Haplogroup O, also known as O-M175, is a human Y-chromosome DNA haplogroup. It is primarily found among populations in Southeast Asia and East Asia. It also is found in various percentages of populations of the Russian Far East, South Asia, Central Asia, Caucasus, Crimea, Ukraine, Iran, Oceania, Madagascar and the Comoros. Haplogroup O is a primary descendant of haplogroup NO-M214.
Haplogroup O-M175 | |
---|---|
Possible time of origin | 41,750 (95% CI 30,597<-> 46,041) years ago[1] 44,700 or 38,300 ybp[2] |
Coalescence age | 33,943 (95% CI 25,124 <-> 37,631) years (Karmin 2022[1]) 35,000 or 30,000 years ago depending on mutation rate[2] |
Possible place of origin | Southeast Asia or East Asia |
Ancestor | NO |
Descendants | Primary: O1 (O-F265); O2 (O-M122) Secondary: O1a (O-M119); O1b (O-M268); O2a (O-M324); O2b (O-F742) |
Defining mutations | M175 (+ numerous other SNPs).[3] |
The O-M175 haplogroup is very common amongst males from East and Southeast Asia. It has two primary branches: O1 (O-F265) and O2 (O-M122). O1 is found at high frequencies amongst males native to Southeast Asia, Taiwan, the Japanese Archipelago, the Korean Peninsula, Madagascar and some populations in southern China and Austroasiatic speakers of India. O2 is found at high levels amongst Han Chinese, Tibeto-Burman populations (including many of those in Yunnan, Tibet, Burma, Northeast India, and Nepal), Manchu, Mongols (especially those who are citizens of the PRC), Koreans, Vietnamese, Filipinos, Japanese, Thais, Polynesians, Miao people, Hmong, the Naiman tribe of Kazakhs in Kazakhstan,[4] Kazakhs in the southeast of Altai Republic,[5] and Kazakhs in the Ili area of Xinjiang.[6]
Origins
editHaplogroup O-M175 is a descendant haplogroup of Haplogroup NO-M214, and first appeared according to different theories either in Southeast Asia (see Rootsi 2006, TMC 1998, Shi 2005, and Bradshaw Foundation) or East Asia (see ISOGG 2012) approximately 40,000 years ago (or between 31,294 and 51,202 years ago according to Karmin et al. 2015).[7][8]
Haplogroup O-M175 is one of NO-M214's two branches. The other is Haplogroup N, which is common throughout North Eurasia.
Distribution
editThis haplogroup appears in high to moderate frequencies in most populations in both East Asia and Southeast Asia, and it is almost exclusive to that region. It is almost nonexistent in Western Siberia, Western Asia, Europe, most of Africa, India and the Americas, where its presence may be the result of recent migrations. However, certain O subclades do achieve significant frequencies among some populations of Central Asia, South Asia, and Oceania. For example, one study found it at a rate of 67% among the Naimans, a tribe in Kazakhstan,[4] even though the rate among Kazakhs in general is only about 3.3% to 10.8%(Wells et al. 2001).[4][9] (It is notable that 75% of cases of haplogroup O-M175 observed in the Kazakh sample of Ashirbekov et al. 2017, of which 10.8% have been found to belong to haplogroup O-M175, have been contributed by the Naimans themselves; only 3.1% of the remainder of the Kazakh sample with the Naimans excluded belong to haplogroup O-M175.) It has been estimated that 25% of the entire male population of the world carries different subclades of O.[8][10] Karafet et al. (2015) have assigned the Y-DNA of 46.2% (12/26) of a sample of Papuan from Pantar Island to haplogroup NO-M214;[11] considering their location in the Malay Archipelago, all or most of these individuals should belong to haplogroup O-M175.
An association with the spread of Austronesian languages in late antiquity is suggested by significant levels of O-M175 among island populations of the South Pacific and Indian Ocean, including the East African littoral. For example, Haplogroup O-M50 has even been found in Bantu-speaking populations of the Comoros along 6% of O-MSY2.2(xM50),[12] while both O-M50 and O-M95(xM88) occur commonly among the Malagasy people of Madagascar with a combined frequency of 34%.[13][14] O-M175 has been found in 28.1% of Solomon Islanders from Melanesia.[15] 12% of Uyghurs (Wells et al. 2001), 6.8% of Kalmyks[16] (17.1% of Khoshuud, 6.1% of Dörwöd, 3.3% of Torguud, 0% of Buzawa), 6.2% of Altaians (Kharkov et al. 2007), 4.1% of Uzbeks on average but Uzbeks from Bukhara 12.1%, Karakalpaks (Uzbekistan) 11.4%, Sinte (Uzbekistans) 6.7% (Wells et al. 2001) and 4.0% of Buryats.[17]
In the Caucasus region it has been found in the Nogais 6%[18] but 5.3% in the Karan Nogais, it is also found in the Dargins of Dargwa speakers at 2.9%.[19] In the Iranic population, it is found in Iranian (Esfahan) at 6.3% (Wells et al. 2001), 8.9% of Tajiks in Afghanistan[20] 4.2% in the Pathans in Pakistan (Firasat 2007) but 1% in Afghanistan,[citation needed] 3.1% in Burusho (Firasat 2007).
Haplogroup O-M175 ranges in various moderate to high frequencies in the ethnic minorities of South Africa. The frequency of this haplogroup is 6.14% in the Cape colored population,[21] 18% in Cape Coloured Muslim, 38% in Cape Indian Muslims and 10% in Cape Other Muslims.[21] It's found 11.5% in the Réunion Creole.[22]
Haplogroup O-M175 had also been found in Latin America and Caribbean as a result of massive Chinese male migration from the 19th century. It was found in the Jamaicans at 3.8%,[23] and in Cubans, 1.5%.[24]
Haplogroup O-M175 has been found in 88.7% of Asian American. 1.6% in Hispanic American, White Americans 0.5%, and 0.3% in African American.[25] Another study gives 0.5% African American.[26]
Among the sub-branches of haplogroup O-M175 are O-M119(O1a), O-M268(O1b), and O-M122(O2).
Y Haplogroup O3-M122 makes up the majority of Jadoon's males, the same haplogroup carried by the majority (50-60%) of Han Chinese. 82.5% of Jadoon men carrying Q-MEH2 and O3-M122 which are both of East Asian origin. O3-M122 was absent in the Sayyid (Syed) population and appeared in low numbers among Tanolis, Gujars and Yousafzais. There appears to be founder affect in the O3-M122 among the Jadoon.[27][28][29] 76.32% of Jadoon men carry O3-M122 while 0.75% of Tanolis, 0.81% of Gujars and 2.82% of Yousafzais carry O3-M122.[30][31]
Russians in China East Asian haplogroup O made up 58% of their Y haplogroup. O3-M122 specifically made up 47% of the Russian sample.[32] The East Asian Y haplogroup O3-M122 was found in 47% of Russian males in China. In another test the East Asian paternal Y Haplogroup O made up 58% of Russian males samples in China.[33]
Haplogroup O was found in 1%-1.2% of Persians in one sample.[34][35][36][better source needed][37][better source needed]
O3-M122 is the commonly shared genetic signature of Sino-Tibetan speaking ethnicities.[38]
O-M175*
editA broad survey of Y-chromosome variation among populations of central Eurasia found haplogroup O-M175(xM119,M95,M122) in 31% (14/45) of a sample of Koreans and in smaller percentages of Crimean Tatars (1/22 = 4.5%), Tajiks (1/16 = 6.25% Dushanbe, 1/40 = 2.5% Samarkand), Uyghurs (2/41 = 4.9%), Uzbeks (1/68 = 1.5% Surxondaryo, 1/70 = 1.4% Xorazm), and Kazakhs (1/54 = 1.9%) (Wells et al. 2001). However, nearly all of the purported Korean O-M175(xM119,M95,M122) Y-chromosomes may belong to Haplogroup O-M176,[Note 1] and later studies do not support the finding of O-M175* among similar population samples (Xue 2006, Kim 2011). The reported examples of O-M175(xM119,M95,M122) Y-chromosomes that have been found among these populations might therefore belong to Haplogroup O-M268*(xM95,M176) or Haplogroup O-M176 (O1b2).
A study published in 2013 found O-M175(xM119, M95, M176, M122) Y-DNA in 5.5% (1/18) Iranians from Teheran, 5.4% (2/37) Tajiks from Badakhshan Province of Afghanistan, and 1/97 Mongols from northwest Mongolia, while finding O-M176 only in 1/20 Mongols from northeast Mongolia.[39]
O-F265 (O1)
editO1a-M119 and O1b-M268 share a common ancestor, O1-F265 (a.k.a. O-F75) approximately 33,181 (95% CI 24,461 to 36,879) YBP.[1][40] O1-F265, in turn, coalesces to a common ancestor with O2-M122 approximately 33,943 (95% CI 25,124 to 37,631) YBP.[1] Thus, O1-F265 should have existed as a single haplogroup parallel to O2-M122 for a duration of approximately 762 years (or anywhere from 0 to 13,170 years considering the 95% CIs and assuming that the phylogeny is correct) before breaking up into its two extant descendant haplogroups, O1-MSY2.2 and O1b-M268.
O-M119 (O1a)
editThis section needs expansion. You can help by adding to it. (December 2012) |
O-M119 (which was known briefly as O-MSY2.2, until the SNP MSY2.2 was found to be unreliable) is found frequently in Austronesian-speaking people, with a moderate distribution in southern and eastern Chinese and Kra-dai peoples.
O-M268 (O1b)
edit- O-K18 Naxi[41]
- O-CTS4040
- O-MF56251 Observed sporadically in China (Guangxi,[41][42] Guangdong,[42] Sichuan,[42] Zhejiang,[42] Jiangsu,[42] Beijing[42]), Thailand (Phuan,[43] Yuan,[43] Central Thai[43]), Vietnam (Nùng,[43] Tày[43])
- O-Page59/CTS10887 Found among North Han Chinese (5%), East Han Chinese (4%), South Han Chinese (3%) [44]
- O-F4070
- O-MF106398 Observed sporadically in China (Guangdong, Henan, Hubei, Jiangxi, Sichuan, Zhejiang, Guangxi, Heilongjiang, Jiangsu, Shandong[42])
- O-F779/F993/F3135 China,[42] Vietnam (Lahu[45]), Qatar[46]
- O-MF107014 Observed sporadically in China (Jiangsu, Anhui, Heilongjiang[42])
- O-CTS5160/MF61620 China (Han,[41] mostly Guangdong or Fujian[42])
- O-F2064/F1759 China (Han from Fujian,[41] Shandong[41]), Singapore,[41] Vietnam (Sila,[45] Hanhi,[45] Kinh[45]), Korea[41]
- O-PH2797/CTS1127 China (especially Shandong, Jiangsu, Liaoning, Hebei, Anhui, Beijing, Henan, and Shanghai[42])
- O-Y148532 China (Shandong, Heilongjiang, Liaoning, Jilin, Jiangsu, Shanghai, Sichuan,[41] Beijing, Shaanxi[42]), Afghanistan (Hazara[41])
- O-Y239146/MF31164 Singapore,[41] Taiwan[41]
- O-Y47392/MF17288 China (Zhejiang[41])
- O-BY182144/Y157814 China (Shandong,[41][42] Gansu[42]), Taiwan[47]
- O-PH4822 China (Beijing,[41] Jiangsu[41])
- O-F417/M1654/CTS469 Japan (Tokyo[41])
- O-CTS9996/PF4341 Philippines[47]
- O-F4070
- O-PK4
- O-F838 Found in about 1.4% of Han Chinese[44] (and esp. in Hunan, Chongqing, Jiangxi, Sichuan, Guizhou[42])
- O-M95
- O-CTS350 China (Ningxia, Yunnan, Heilongjiang, Hunan, Shaanxi, Anhui, etc.[42])
- O-M1310
- O-Y172653/Y172877 Found in China (esp. Zhejiang, Fujian, Guangdong, Sichuan, Hunan, Jiangxi, Hubei, Chongqing[42]) and Japan[42]
- O-F1803/M1348 China (Zhejiang, Shandong, Beijing, Guangdong, Hubei, Sichuan, Jiangsu, Shanghai, etc.[42])
- O-ACT721/ACT1038 Found sporadically in China (Zhejiang,[42] Anhui,[42] Hunan,[42] Hainan,[41] Tianjin,[42] Beijing,[42] Liaoning,[41] Heilongjiang[42])
- O-F789/M1283 Found in China (Blang,[49] Palaung,[49] Wa,[49] Dai,[41][50] Yi,[41][50] Naxi), Vietnam, Cambodia, Singapore (Malay), Java, Borneo, Thailand, Laos, Myanmar, Bhutan, Bangladesh, India (Tripura, Ho, Konda Dora, Gond)
- O-M1283* Lao Isan[51]
- O-MF600645 Gansu (Hui,[41] Dongxiang[42]), Sichuan (Chengdu[42]), Hunan (Yiyang[42])
- O-M1368 Singapore[41]
- O-M1361
- O-MF611153 Found sporadically in China (Hunan, Hubei, Chongqing, Guangxi, Jiangxi[42])
- O-A22938 Vietnam (Kinh from Ho Chi Minh City[41]), China (Hong Kong,[41] Qinzhou,[42] Chongqing,[42] Lijiang[42])
- O-Y9322 China (Dai in Xishuangbanna,[41] Yunnan,[42] Chongqing,[42] Guangdong,[42] Sichuan,[42] etc.)
- O-Y9325
- O-Z39485 China (Dai, Yi)[41]
- O-Z39490
- O-Y9033/B426 Laos (Laotian[51]), Thailand (Blang,[51] Khmu,[51] Lawa,[51] Htin,[51] Padaung Karen,[51] Tai Dam,[51] Suay,[51] Khmer,[51] Mon,[51] Lao Isan,[51] Soa,[51] Shan,[51] Phutai,[51] Nyaw,[51] S'gaw Karen,[51] Thai,[51] Khon Mueang[51]), Vietnam (Mang from Mường Tè District,[45] Ede from Krông Buk District and Tuy An District,[45] Kinh from Hoàng Mai District, Gia Lâm District, and Yên Phong District,[45] Thái from Điện Biên Phủ,[45] Giarai from Ayun Pa[45])
- O-Y9325
- O-M1361
- O-F1252
- O-SK1630/F5504 China (esp. Sichuan and Guizhou, accounting for about 0.25% of the entire Chinese population[42])
- O-ACT5802
- O-MF92614
- O-F16061
- O-MF286118 Found in two Han Chinese from Guangdong[42]
- O-F19607
- O-ACT5802
- O-F2924
- O-CTS5854
- O-Z23810
- O-CTS7399
- O-Y85641 Japan (Tokyo[41]), China (esp. Shandong, Liaoning, Jilin, Heilongjiang[42])
- O-FGC19713/Y14026 Laos (Laotian in Vientiane and Luang Prabang[51]), Thailand (Tai Dam,[51] Tai Lue,[51] Nyah Kur,[51] Thai,[51] Eastern Lawa[51]), Vietnam (Thái from Bá Thước District and Tủa Chùa District,[45] Hà Nhì from Mường Tè District[45])
- O-FGC19707
- O-MF14427 China (esp. Jiangsu, Gansu, Henan, Shandong, Shanxi, Hebei, Shaanxi[42])
- O-FGC19716 China (Hong Kong,[41] Guangdong,[42] Hunan,[42] Chongqing[42])
- O-FGC19718 China (esp. Fujian, Jiangxi, Hubei, Jiangsu, Guangdong[42]), Philippines (Capiz[41])
- O-Z23849 China (Chongqing Han,[41] Xishuangbanna Dai,[41] Guangxi Zhuang,[41] Guangdong,[41] Shandong,[41] Tianjin[41])
- O-FGC19707
- O-CTS651/CTS10484 Thailand (Tai Khün,[51] Phuan,[51] Tai Lue,[51] Khon Mueang,[51] Eastern Lawa,[51] Lao Isan,[51] Thai[51]), Laos (Laotian in Vientiane[51]), Vietnam (Dao and Nùng from Hoàng Su Phì District,[45] Tày from Krông Pắk District, Hà Quảng District, and Đình Lập District[45])
- O-CTS7399
- O-Z23781 China (Henan[41])
- O-Z23810
- O-M111/M88 Found frequently among Vietnamese,[53][54][45] Tai peoples[55][56][54][45] (Bouyei,[55] Zhuang,[57][58][56] Nùng,[45] Tày,[45] Thái people in Vietnam,[45] Lao,[59] Northeastern Thai,[57] Northern Thai,[60][59] general population of Bangkok[54]), Lachi,[45] Lô Lô,[45] Hani-Akha,[55][54][45] Bunu,[61] She people,[53] Cambodians,[57] Kuy,[49][61] Bru,[61] and Htin,[49] with a moderate distribution among Qiang,[55] Bai,[62] Yi,[56] Bamar,[63] Jingpo,[63] Lahu,[45] Tujia,[57] Han Chinese,[57][55][53][54] Miao,[53][61] Pathen,[45] Yao,[55][53][61][45] Hlai,[57][55] Taiwanese aborigines[13][53][54] (especially Bunun[60][54]), the Philippines,[53][54] Malaysia[53] (Kota Kinabalu[13]), Kalimantan (Banjarmasin[13]), Java,[54] Chamic-speaking peoples (Cham from Bình Thuận,[59] Ede,[45] Jarai[45]), and Kiribati[60]
- O-M111/M88* Northern Thailand (Htin, Lawa), Cambodia (Jarai, Brao, Kachac, Khmer, Lao, Lun), Yunnan (De'ang)[49]
- O-F2524
- O-F2524* Jiangsu[41]
- O-F2346
- O-F2890 Thailand (Khon Mueang,[51] Phuan,[51] Shan,[51] Htin,[51] Tai Dam,[51] Thai,[51] Lawa,[51] Lao Isan,[51] Mon[51]), Vietnam (Kinh from Gia Lâm District,[45] Tày from Lục Yên District[45])
- O-F2890* Ho Chi Minh City[41]
- O-Z24048
- O-F2758 Vietnam (Kinh,[45] Lahu,[45] Dao, Pathen,[45] Tày,[45] Thái,[45] Ede,[45] Giarai[45]), Cambodia (Kuy, Tampuan, Khmer), Thailand (Phutai,[51] Bru,[51] Tai Khün,[51] Phuan,[51] Tai Dam,[51] Shan,[51] Khon Mueang,[51] Mon,[51] Lao Isan,[51] Tai Lue,[51] Htin,[49][51] Lawa,[49] Khmu,[51] Kaleun,[51] Nyaw,[51] Suay,[51] Thai[51]), Laos (Laotian in Luang Prabang[51]), Yunnan (Bulang, De'ang)[49]
- O-F2758* China (Miao,[41] Hunan[41])
- O-Z24083
- O-Z24083* Ho Chi Minh City (Kinh)
- O-Z24089
- O-SK1627/Z24091 Vietnam (Lô Lô from Mèo Vạc District,[45] La Chí and Nùng from Hoàng Su Phì District,[45] Hà Nhì from Mường Tè District,[45] Tày from Chợ Đồn District and Đăk Mil District,[45] Ede from Ea Kar District,[45] Kinh from Nghĩa Hưng District[45]), Thailand (Soa,[51] Saek,[51] Phutai,[51] Suay,[51] Tai Dam,[51] S'gaw Karen,[51] Nyah Kur,[51] Khmer,[51] Lawa,[51] Lao Isan,[51] Mon,[51] Thai[51]), Laos (Laotian in Vientiane[51])
- O-Z24091* China (Hebei,[41] Xishuangbanna Dai[41]), Vietnam (Kinh from Ho Chi Minh City[41])
- O-Y26364
- O-Y26364* Thailand (Phutai from Sakon Nakhon Province[51][41])
- O-Y26370 China (Tujia[41]), Vietnam (Kinh from Ho Chi Minh City[41])
- O-F923
- O-SK1627/Z24091 Vietnam (Lô Lô from Mèo Vạc District,[45] La Chí and Nùng from Hoàng Su Phì District,[45] Hà Nhì from Mường Tè District,[45] Tày from Chợ Đồn District and Đăk Mil District,[45] Ede from Ea Kar District,[45] Kinh from Nghĩa Hưng District[45]), Thailand (Soa,[51] Saek,[51] Phutai,[51] Suay,[51] Tai Dam,[51] S'gaw Karen,[51] Nyah Kur,[51] Khmer,[51] Lawa,[51] Lao Isan,[51] Mon,[51] Thai[51]), Laos (Laotian in Vientiane[51])
- O-F2890 Thailand (Khon Mueang,[51] Phuan,[51] Shan,[51] Htin,[51] Tai Dam,[51] Thai,[51] Lawa,[51] Lao Isan,[51] Mon[51]), Vietnam (Kinh from Gia Lâm District,[45] Tày from Lục Yên District[45])
- O-CTS5854
- O-SK1630/F5504 China (esp. Sichuan and Guizhou, accounting for about 0.25% of the entire Chinese population[42])
- O-CTS4040
- O-M176
- O-K4: Found frequently among Koreans and with a moderate distribution among Japanese, Ryukyuans, Daurs, Evenks, Hezhe, Manchus, and Sibe. Also found sporadically (<1%) among Han Chinese, Hui, Micronesians, Mongols, Thais, Uyghurs, Vietnamese, etc.
- O-47z: Found frequently among Japanese and Ryukyuans and with a moderate distribution among Koreans. Found sporadically (<1%) among Manchus, Mongols, Han Chinese, Hui, Tujia, Vietnamese, etc.
O-M122 (O2)
editFound frequently among populations of East Asia, Southeast Asia, and culturally Austronesian regions of Oceania, with a moderate distribution in Central Asia (Shi 2005).
- O-M122
- O-CTS1754 East & Southeast Asia
- O-M324
- O-L465
- O-CTS727
- O-F915
- O-CTS3709
- O-JST002611/CTS2483
- O-CTS2483* China,[47] Japan,[47] Philippines[47]
- O-CTS10573 Beijing,[64] Sichuan,[64] Henan,[64] Jiangsu[64]
- O-F18
- O-CTS498 China,[41] Japan (Tokyo)[41]
- O-F449 Azerbaijan[47]
- O-F117
- O-F117* Fujian[41]
- O-F11
- O-F11* Gansu,[41] Japanese[41]
- O-F930 Beijing,[41] Armenia,[41] Inner Mongolia,[64] Hebei,[64] Shaanxi,[64] Shandong,[64] Zhejiang,[64] Hubei[64]
- O-F2685 Beijing, Shanghai, Fujian, Guangdong[64]
- O-BY169374
- O-F539 Beijing, Shanghai, Jiangsu, Zhejiang, Jiangxi, Guangdong, Yunnan[64]
- O-CTS12877
- O-Y29837
- O-BY36917 Japan[47]
- O-F4062 Beijing, Shanghai, Guangdong, Jiangsu, Shandong, Shaanxi, Chongqing, Heilongjiang, Liaoning, Henan, Hubei, Hunan, Zhejiang[64]
- O-Y15976 China, Japan,[47] Korea, Pakistan, Vietnam
- O-FGC54474
- O-F971 Beijing, Shanghai, Hubei, Guangdong[64]
- O-F632
- O-F632* Beijing[41]
- O-F16340 Zhejiang[41]
- O-F133 China, Bulgaria[47]
- O-CTS727
- O-P201
- O-M188
- O-M188* Korea[47]
- O-CTS800
- O-CTS445
- O-CTS201 Korea[47]
- O-M159 China (about 0.79% of the national male population[65]), Taiwan, Cambodia, Malaysia, Singapore[47]
- O-FTA21663/O-MF22947 China (Heilongjiang,[41][42] Inner Mongolia,[41][42] Zhejiang,[42] Shanghai,[42] Henan,[42] Hebei,[42] etc.; accounts for about 0.06% of the male population in China at present[66]), Saudi Arabia (al-Qaṣīm[41])
- O-CTS3994
- O-MF18110/FGC50590 China (esp. Guangdong, Zhejiang, Hunan, Shandong, and Guangxi[42])
- O-MF109844
- O-FGC50661 China (esp. Jiangsu and Hunan[42])
- O-MF56709
- O-FGC50643/MF15475 China (Shandong,[42] Hebei,[42] Hubei,[42] Shanxi,[41][42] Anhui,[42] Jiangsu,[42] etc.)
- O-MF56474 China (Jiangsu, Anhui, Jilin, Shandong, etc.[42])
- O-FGC50649
- O-Y169670/O-MF14256 China (esp. Jiangsu,[41][42] Shandong,[42] Zhejiang,[42] and Shanghai[42])
- O-MF50824
- O-MF14135/O-Z12303 China (currently accounts for about 0.44% of the total male population[68])
- O-MF238642
- O-MF37094 China (Zhejiang,[42] Jiangsu[42])
- O-Y169696/O-MF15693 China (Jiangsu,[41][42] Fufeng County,[42] Beijing,[42] Tangshan,[42] Feidong County,[42] Chifeng,[42] Xi County,[42] Min County,[42] Laizhou,[42] Rushan,[42] Harbin,[42] Yanji,[42] Dancheng County[42])
- O-MF18577/O-MF18626 China (currently accounts for about 0.23% of all males in China, especially in Jiangsu [1.08%], Shanghai [0.69%], Ningxia [0.39%], Shandong [0.38%], Anhui [0.33%], Heilongjiang [0.32%], Zhejiang [0.31%], and Jilin [0.26%][69]), Kazakhstan,[70] Thailand[70]
- O-MF238642
- O-FGC50558 Japan,[47] Korea[47]
- O-Y169670/O-MF14256 China (esp. Jiangsu,[41][42] Shandong,[42] Zhejiang,[42] and Shanghai[42])
- O-M159 China (about 0.79% of the national male population[65]), Taiwan, Cambodia, Malaysia, Singapore[47]
- O-M7 Found frequently among human remains associated with the Neolithic Daxi culture[71] and modern Hmong–Mien, Katuic, and Bahnaric peoples,[61] with a moderate distribution among Han Chinese (Xue 2006), Buyei (Xue 2006), Bai (Wen 2004), Mosuo (Wen 2004), Tibetans (Wen 2004), Qiang (Xue 2006), Oroqen (Xue 2006), Tujia (Su 2000), Thai (Su 2000), Orang Asli (Su 2000), western Indonesians (Su 2000 and Kayser 2008), Malaysians (Kayser 2008), Vietnamese (Kayser 2008), and Atayal (Su 2000).
- O-MF106687 China (Jinghu District,[42] etc.)
- O-Z25245
- O-MF9858/O-Z6157 China (approximately 0.08% of all males in present-day China[72]), Thailand (Central Thai in Central Thailand[51][43])
- O-Y26422
- O-F1276
- O-F1863
- O-MF107102 China (Tongchuan District[42])
- O-MF56735 China (Haiyan County, Suzhou, Wuxi, Shanghai, etc.[42])
- O-MF36531 China (Han in Yanping District[42])
- O-Y13816
- O-MF109664 China (Kazakh in Minqin County,[43] Kazakh in Tacheng City,[42] Han in Zizhong County,[42] Han in Furong District[42])
- O-MF36502 Guangdong (Kaiping, Yangjiang, Foshan, Lianjiang, etc.[42])
- O-Y13816
- O-F1134
- O-MF35799/O-Y94171 Thailand (Mon in Central Thailand[51][43]), China (observed sporadically in Pingyang County, Yunan County, Siming District, Longyao County, Shanwei, etc.[42])
- O-F1262/O-Y173492 China[41][70] (accounts for about 0.15% of the male population in China at present and is relatively concentrated in Zhejiang, Taiwan, Anhui, Jiangxi, etc.;[73] also observed in individuals from Zhenjiang,[43] Hejian,[43] and Langfang[43])
- O-FT303223/O-MF106843/O-F15314/O-F20756 China[70] (Changsha,[42] Chancheng District,[42] Wanzhou District,[42] Chaoyang District,[42] Dongying,[42] Chifeng,[42] Liaoyuan,[42] Harbin,[42] Han in Zhengzhou,[43] Dai in Xishuangbanna[41]), Thailand[70] (Khon Mueang in Northern Thailand,[51][43] Black Tai in Loei Province[51][43])
- O-Z25288/O-Z25293 Vietnam[70] (Kinh in Ho Chi Minh City,[41][43] Hanoi,[43] Nam Dinh,[43] and Lao Cai,[43] Giarai in Gia Lai,[43] Tày in Thai Nguyen[43])
- O-CTS6489
- O-MF106428/O-Y94472/O-FTB23660 Thailand[70] (Phayao,[41] Phutai, Lao Isan, Tai Lue, Phuan, Shan, Khon Mueang/Tai Yuan, Khmer, Mon[43]), Vietnam[70] (Tày in Lào Cai[43]), China (Dai in Xishuangbanna,[41] Achang in Yunnan;[43] accounts for about 0.05% of all males in China at present, mainly distributed in Guangxi and Guangdong[74])
- O-F1275 Guangxi (Dushan 4-1 ca. 7024 - 6643 BCE[70])
- O-MF15199/O-FTA25885
- O-F20472
- O-FTB23785 Thailand,[70] Vietnam[70]
- O-F17410/O-F18833/O-MF122643/O-BY177553 Thailand (Lao Isan in Northeast Thailand[51][43])
- O-MF106415/O-MF111486/O-BY122399 Thailand[70] (Shan in Mae Hong Son Province[75][43]), China (observed sporadically in individuals from Hubei, Hunan, Chongqing, Sichuan, Guangxi, Jiangxi, Zhejiang, Jiangsu, Anhui, Gansu, Shaanxi, Shanxi, Henan, and Shandong[42])
- O-Y127482/O-F15988 Thailand (Nyahkur and Lao Isan in Northeast Thailand[51][43])
- O-MF6534/O-MF58872/O-BY27925/O-Y23477 Thailand[70] (Central Thai in Central Thailand, Phuan in Central Thailand, Khon Mueang in North Thailand,[51][43] White Hmong in Chiang Rai Province[75][43]), Singapore,[41][43] China (Guangdong, Guangxi, Hunan, Sichuan, Jiangxi, Zhejiang, Shaanxi, Henan, Shandong[43][42])
- O-CTS6579
- O-CTS123/O-F22573/O-MF48275 China (Hunan Han;[41] accounts for about 0.13% of the male population in China at present, mainly distributed in Jiangxi, Hunan and other south-central provinces and cities[76])
- O-F14832/O-F15788/O-Y208219 China[70] (accounts for about 0.22% of the male population in China at present, mainly distributed in the northern region[77]), Thailand[70] (Mon in Western Thailand,[51][43] Tai Lue in Northern Thailand[51][43])
- O-F20472
- O-Z25411
- O-ACT1126/O-Y140772/O-F1289 China (relatively concentrated in northern China at present, accounting for about 0.24% of the national male population;[78] also found in Fujian[41]), Thailand[70] (Lisu[43])
- O-Z25398
- O-F22005/O-Z25400 Thailand[70] (Black Hmong in North Thailand[41][75]), Vietnam[70] (Kinh in Ho Chi Minh City[41]), China (currently distributed mainly in Guangxi, Sichuan, Guangdong and other places, accounting for about 0.10% of the national male population[79])
- O-F1100/O-Y37861 Hunan[41]
- O-MF17697 Laos,[70] Thailand,[70] China (Jiangsu, Hunan, Jiangxi, Guangxi, Guangdong, Guizhou, Yunnan, Fujian, Sichuan, Hong Kong, Chongqing, Henan, Liaoning[42])
- O-F1234/O-Y37855
- O-Y185160/O-MF36985 Hebei,[41] Beijing,[41] Sichuan, Shaanxi, Guangxi, Zhejiang, Shandong, Ningxia, Inner Mongolia, Hubei, Jiangxi (currently accounts for approximately 0.13% of the Chinese male population[80])
- O-FGC71370
- O-MF193618 Sichuan, Zhejiang, Shandong, Anhui, Hunan, Hubei, Fujian (currently accounts for about 0.08% of the male population in China, mainly distributed in Guangdong, Hunan, Anhui and other provinces and cities[81]), Philippines[70]
- O-F14904/N5 Ningxia,[41] Hmong (Northern Thailand[75]), She,[41] Iu Mien (Phayao Province[75]), Quebec[41]. Huang et al. (2022) found that this is the most common Y-chromosome haplogroup among many Hmongic-speaking ethnic groups (including Guangxi Miao, Hunan Miao, Hunan Pa-hng, and Thailand Hmong), with a frequency of 47.1% among the Guangxi Miao.[82]
- O-MF15199/O-FTA25885
- O-F1863
- O-CTS201 Korea[47]
- O-P164
- O-F996/F3237
- O-A16433 Heilongjiang[41]
- O-MF56976 Anhui[41]
- O-Y125645
- O-F871
- O-F706 Philippines, China, Cambodia,[47] Thailand (Bru in Sakon Nakhon Province[51])
- O-F1010 Thailand (Eastern Lawa, Blang, Palaung, Khon Mueang from Chiang Rai Province[51])
- O-AM01750/AM01861/B451 Singapore (Malay),[7] Indonesia (Bajo),[7] Philippines (Batak)[7]
- O-F2472
- O-F706 Philippines, China, Cambodia,[47] Thailand (Bru in Sakon Nakhon Province[51])
- O-A16433 Heilongjiang[41]
- O-M134: Found frequently among speakers of Sino-Tibetan languages, among members of the Kazakh Naiman tribe with a moderate distribution throughout East Asia and Southeast Asia.[citation needed]
- O-Y20/PAGES00125 Poland[47]
- O-F1725
- O-Y12/F314
- O-Y12* Beijing (Han)[41]
- O-CTS2643/CTS11192
- O-CTS53
- O-F876
- O-F275
- O-F634
- O-CTS3776/F2887
- O-M117/PAGE23
- O-MF1380/CTS4960 China, Korea, Japan,[47] Indonesia[47]
- O-M133/M1706 Shandong[41]
- O-M1706* Japan (Tokyo)[41]
- O-YP4864
- O-CTS7634
- O-M1726
- O-A9459
- O-F6800
- O-F14249
- O-F438 Japan (Tokyo)[41]
- O-CTS1642
- O-Y20/PAGES00125 Poland[47]
- O-F996/F3237
- O-M188
- O-L465
O-M324 (O2a)
editThis section needs expansion. You can help by adding to it. (December 2017) |
O-F742 (O2b)
editThis section needs expansion. You can help by adding to it. (December 2017) |
Language families and genes
editHaplogroup O is associated with populations which speak Austric languages. The following is a phylogenetic tree of language families and their corresponding SNP markers, or haplogroups, sourced mainly from Edmondson 2007 and Shi 2005. This has been called the "Father Tongue Hypothesis" by George van Driem (van Driem 2011). It does not appear to account for O-M176, which is found among Japanese, Korean, and Manchurian males.
(M175) |
| ||||||||||||||||||
Phylogenetics
editPhylogenetic history
editPrior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being, above all, timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.
YCC 2002/2008 (Shorthand) | (α) | (β) | (γ) | (δ) | (ε) | (ζ) | (η) | YCC 2002 (Longhand) | YCC 2005 (Longhand) | YCC 2008 (Longhand) | YCC 2010r (Longhand) | ISOGG 2006 | ISOGG 2007 | ISOGG 2008 | ISOGG 2009 | ISOGG 2010 | ISOGG 2011 | ISOGG 2012 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
O-M175 | 26 | VII | 1U | 28 | Eu16 | H9 | I | O* | O | O | O | O | O | O | O | O | O | O |
O-M119 | 26 | VII | 1U | 32 | Eu16 | H9 | H | O1* | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a |
O-M101 | 26 | VII | 1U | 32 | Eu16 | H9 | H | O1a | O1a1 | O1a1a | O1a1a | O1a1 | O1a1 | O1a1a | O1a1a | O1a1a | O1a1a | O1a1a |
O-M50 | 26 | VII | 1U | 32 | Eu16 | H10 | H | O1b | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 |
O-P31 | 26 | VII | 1U | 33 | Eu16 | H5 | I | O2* | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 |
O-M95 | 26 | VII | 1U | 34 | Eu16 | H11 | G | O2a* | O2a | O2a | O2a | O2a | O2a | O2a | O2a | O2a | O2a1 | O2a1 |
O-M88 | 26 | VII | 1U | 34 | Eu16 | H12 | G | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1a | O2a1a |
O-SRY465 | 20 | VII | 1U | 35 | Eu16 | H5 | I | O2b* | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b |
O-47z | 5 | VII | 1U | 26 | Eu16 | H5 | I | O2b1 | O2b1a | O2b1 | O2b1 | O2b1a | O2b1a | O2b1 | O2b1 | O2b1 | O2b1 | O2b1 |
O-M122 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3* | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 |
O-M121 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3a | O3a | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1a | O3a1a |
O-M164 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3b | O3b | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a1b | O3a1b |
O-M159 | 13 | VII | 1U | 31 | Eu16 | H6 | L | O3c | O3c | O3a3a | O3a3a | O3a3 | O3a3 | O3a3a | O3a3a | O3a3a | O3a3a | O3a3a |
O-M7 | 26 | VII | 1U | 29 | Eu16 | H7 | L | O3d* | O3c | O3a3b | O3a3b | O3a4 | O3a4 | O3a3b | O3a3b | O3a3b | O3a2b | O3a2b |
O-M113 | 26 | VII | 1U | 29 | Eu16 | H7 | L | O3d1 | O3c1 | O3a3b1 | O3a3b1 | - | O3a4a | O3a3b1 | O3a3b1 | O3a3b1 | O3a2b1 | O3a2b1 |
O-M134 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e* | O3d | O3a3c | O3a3c | O3a5 | O3a5 | O3a3c | O3a3c | O3a3c | O3a2c1 | O3a2c1 |
O-M117 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e1* | O3d1 | O3a3c1 | O3a3c1 | O3a5a | O3a5a | O3a3c1 | O3a3c1 | O3a3c1 | O3a2c1a | O3a2c1a |
O-M162 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e1a | O3d1a | O3a3c1a | O3a3c1a | O3a5a1 | O3a5a1 | O3a3c1a | O3a3c1a | O3a3c1a | O3a2c1a1 | O3a2c1a1 |
Original Research Publications
editThe following research teams per their publications were represented in the creation of the YCC Tree.
Phylogenetic trees
editISOGG 2017 tree (ver. 12.244).[86]
- O (M175)
- O1 (F265/M1354, CTS2866, F75/M1297, F429/M1415, F465/M1422)
- O1a (M119)
- O1a1 (B384/Z23193)
- O1a1a (M307.1/P203.1)
- O1a1a1 (F446)
- O1a1a1a (F140)
- O1a1a1a1 (F78)
- O1a1a1a1a (F81)
- O1a1a1a1a1 (CTS2458)
- O1a1a1a1a1a (F533)
- O1a1a1a1a1a1 (F492)
- O1a1a1a1a1a1a (F656)
- O1a1a1a1a1a1a1 (A12440)
- O1a1a1a1a1a1a1a (A12439)
- O1a1a1a1a1a1a2 (A14788)
- O1a1a1a1a1a1a3 (F65)
- O1a1a1a1a1a1a4 (MF1068)
- O1a1a1a1a1a1a5 (Z23482)
- O1a1a1a1a1a1a1 (A12440)
- O1a1a1a1a1a1b (FGC66168)
- O1a1a1a1a1a1b1 (CTS11553)
- O1a1a1a1a1a1c (Y31266)
- O1a1a1a1a1a1c1 (Y31261)
- O1a1a1a1a1a1d (A12441)
- O1a1a1a1a1a1e (MF1071)
- O1a1a1a1a1a1e1 (MF1074)
- O1a1a1a1a1a1a (F656)
- O1a1a1a1a1a2 (CTS4585)
- O1a1a1a1a1a1 (F492)
- O1a1a1a1a1a (F533)
- O1a1a1a1a2 (MF1075)
- O1a1a1a1a1 (CTS2458)
- O1a1a1a1a (F81)
- O1a1a1a2 (YP4610/Z39229)
- O1a1a1a2a (AM00330/AMM480/B386)
- O1a1a1a2a1 (AM00333/AMM483/B387)
- O1a1a1a2a1a (B388)
- O1a1a1a2a1 (AM00333/AMM483/B387)
- O1a1a1a2b (SK1555)
- O1a1a1a2a (AM00330/AMM480/B386)
- O1a1a1a1 (F78)
- O1a1a1b (SK1568/Z23420)
- O1a1a1b1 (M101)
- O1a1a1b2 (Z23392)
- O1a1a1b2a (Z23442)
- O1a1a1b2a1 (SK1571)
- O1a1a1b2a (Z23442)
- O1a1a1a (F140)
- O1a1a2 (CTS52)
- O1a1a2a (CTS701)
- O1a1a2a1 (K644/Z23266)
- O1a1a2a (CTS701)
- O1a1a1 (F446)
- O1a1b (CTS5726)
- O1a1a (M307.1/P203.1)
- O1a2 (M110)
- O1a2a (F3288)
- O1a2a1 (B392)
- O1a2a1a (B393)
- O1a2a1 (B392)
- O1a2a (F3288)
- O1a3 (Page109)
- O1a1 (B384/Z23193)
- O1b (M268)
- O1b1 (F2320)
- O1b1a (M1470)
- O1b1a1 (PK4)
- O1b1a1a (M95)
- O1b1a1a1 (F1803/M1348)
- O1b1a1a1a (F1252)
- O1b1a1a1a1 (F2924)
- O1b1a1a1a1a (M111)
- O1b1a1a1a1a1 (F2758)
- O1b1a1a1a1a1a (Z24083)
- O1b1a1a1a1a1a1 (Z24089)
- O1b1a1a1a1a1a1a (F923)
- O1b1a1a1a1a1a1a1 (CTS2022)
- O1b1a1a1a1a1a1a1a (F1399)
- O1b1a1a1a1a1a1a1a1 (F2415)
- O1b1a1a1a1a1a1a1a (F1399)
- O1b1a1a1a1a1a1a2 (Z24131)
- O1b1a1a1a1a1a1a3 (Z24100)
- O1b1a1a1a1a1a1a1 (CTS2022)
- O1b1a1a1a1a1a1b (SK1627/Z24091)
- O1b1a1a1a1a1a1b1 (Z39410)
- O1b1a1a1a1a1a1a (F923)
- O1b1a1a1a1a1a2 (Z24088)
- O1b1a1a1a1a1a1 (Z24089)
- O1b1a1a1a1a1a (Z24083)
- O1b1a1a1a1a2 (F2890)
- O1b1a1a1a1a2a (Z24048)
- O1b1a1a1a1a2a1 (Z24050)
- O1b1a1a1a1a2b (Z24014)
- O1b1a1a1a1a2a (Z24048)
- O1b1a1a1a1a1 (F2758)
- O1b1a1a1a1b (CTS5854)
- O1b1a1a1a1b1 (Z23810)
- O1b1a1a1a1b1a (CTS7399)
- O1b1a1a1a1b1a1 (FGC19713/Y14026)
- O1b1a1a1a1b1a1a (Z23849)
- O1b1a1a1a1b1a1a1 (FGC61038)
- O1b1a1a1a1b1a1a (Z23849)
- O1b1a1a1a1b1a1 (FGC19713/Y14026)
- O1b1a1a1a1b1b (CTS651)
- O1b1a1a1a1b1b1 (CTS9884)
- O1b1a1a1a1b1a (CTS7399)
- O1b1a1a1a1b2 (F4229)
- O1b1a1a1a1b2a (F809)
- O1b1a1a1a1b2a1 (F2517)
- O1b1a1a1a1b2a (F809)
- O1b1a1a1a1b1 (Z23810)
- O1b1a1a1a1a (M111)
- O1b1a1a1a2 (SK1630)
- O1b1a1a1a2a (SK1636)
- O1b1a1a1a1 (F2924)
- O1b1a1a1b (F789/M1283)
- O1b1a1a1b1 (FGC29900/Y9322/Z23667)
- O1b1a1a1b1a (B426/FGC29896/Y9033/Z23671)
- O1b1a1a1b1a1 (FGC29907/YP3930)
- O1b1a1a1b1a2 (B427/Z23680)
- O1b1a1a1b1b (Z39485)
- O1b1a1a1b1c (B418)
- O1b1a1a1b1a (B426/FGC29896/Y9033/Z23671)
- O1b1a1a1b2 (SK1646)
- O1b1a1a1b1 (FGC29900/Y9322/Z23667)
- O1b1a1a1a (F1252)
- O1b1a1a2 (CTS350)
- O1b1a1a3 (Page103)
- O1b1a1a1 (F1803/M1348)
- O1b1a1b (F838)
- O1b1a1b1 (F1199)
- O1b1a1a (M95)
- O1b1a2 (Page59)
- O1b1a2a (F993)
- O1b1a2a1 (F1759)
- O1b1a2a1a (CTS1127)
- O1b1a2a1 (F1759)
- O1b1a2b (F417/M1654)
- O1b1a2b1 (F840)
- O1b1a2b1a (F1127)
- O1b1a2b2 (CTS1451)
- O1b1a2b1 (F840)
- O1b1a2c (CTS9996)
- O1b1a2a (F993)
- O1b1a1 (PK4)
- O1b1a (M1470)
- O1b2 (P49, M176)
- O1b2a (F1942/Page92)
- O1b2a1 (CTS9259)
- O1b2a1a (F1204)
- O1b2a1a1 (CTS713)
- O1b2a1a1a (CTS1875)
- O1b2a1a1a1 (CTS10682)
- O1b2a1a1b (Z24598)
- O1b2a1a1c (CTS203)
- O1b2a1a1a (CTS1875)
- O1b2a1a2 (F2868)
- O1b2a1a2a (L682)
- O1b2a1a2a1 (CTS723)
- O1b2a1a2a1a (CTS7620)
- O1b2a1a2a1b (A12446)
- O1b2a1a2a1b1 (PH40)
- O1b2a1a2a1 (CTS723)
- O1b2a1a2b (F940)
- O1b2a1a2a (L682)
- O1b2a1a3 (CTS10687)
- O1b2a1a3a (CTS1215)
- O1b2a1a1 (CTS713)
- O1b2a1b (CTS562)
- O1b2a1a (F1204)
- O1b2a2 (Page90)
- O1b2a1 (CTS9259)
- O1b2a (F1942/Page92)
- O1b1 (F2320)
- O1a (M119)
- O2 (M122)
- O2a (M324)
- O2a1 (L127.1)
- O2a1a (F1876/Page127)
- O2a1a1 (F2159)
- O2a1a1a (F1867/Page124)
- O2a1a1a1 (F852)
- O2a1a1a1a (F2266)
- O2a1a1a1a1 (L599)
- O2a1a1a1a1a (Z43961)
- O2a1a1a1a1a1 (Z43963)
- O2a1a1a1a1a (Z43961)
- O2a1a1a1a1 (L599)
- O2a1a1a1b (F854)
- O2a1a1a1b1 (Z43966)
- O2a1a1a1c (Page130)
- O2a1a1a1a (F2266)
- O2a1a1a1 (F852)
- O2a1a1b (F915)
- O2a1a1b1 (F1478)
- O2a1a1b1a (PF5390)
- O2a1a1b1a1 (CTS1936)
- O2a1a1b1a1a (Z43975)
- O2a1a1b1a2 (FGC33994)
- O2a1a1b1a (PF5390)
- O2a1a1b1 (F1478)
- O2a1a1a (F1867/Page124)
- O2a1a1 (F2159)
- O2a1b (M164)
- O2a1c (IMS-JST002611)
- O2a1c1 (F18)
- O2a1c1a (F117)
- O2a1c1a1 (F13)
- O2a1c1a1a (F11)
- O2a1c1a1a1 (F632)
- O2a1c1a1a1a (F110/M11115)
- O2a1c1a1a1a1 (F17)
- O2a1c1a1a1a1a (F377)
- O2a1c1a1a1a1a1 (F1095)
- O2a1c1a1a1a1a1a (F856)
- O2a1c1a1a1a1a1a1 (F1418)
- O2a1c1a1a1a1a1a2 (Z25097)
- O2a1c1a1a1a1a1a (F856)
- O2a1c1a1a1a1a2 (CTS7501)
- O2a1c1a1a1a1a1 (F1095)
- O2a1c1a1a1a1b (F793)
- O2a1c1a1a1a1a (F377)
- O2a1c1a1a1a2 (Y20951)
- O2a1c1a1a1a2a (Y20932)
- O2a1c1a1a1a1 (F17)
- O2a1c1a1a1a (F110/M11115)
- O2a1c1a1a2 (F38)
- O2a1c1a1a3 (F12)
- O2a1c1a1a4 (F930)
- O2a1c1a1a4a (F2685)
- O2a1c1a1a5 (F1365/M5420/PF1558)
- O2a1c1a1a5a (Y15976)
- O2a1c1a1a5a1 (Y16154)
- O2a1c1a1a5a1a (Y26383)
- O2a1c1a1a5a1a1 (SK1686)
- O2a1c1a1a5a1a (Y26383)
- O2a1c1a1a5a1 (Y16154)
- O2a1c1a1a5b (FGC54486)
- O2a1c1a1a5b1 (FGC54507)
- O2a1c1a1a5a (Y15976)
- O2a1c1a1a6 (CTS12877)
- O2a1c1a1a6a (F2527)
- O2a1c1a1a6a1 (CTS5409)
- O2a1c1a1a6a2 (F2941)
- O2a1c1a1a6a (F2527)
- O2a1c1a1a7 (F723)
- O2a1c1a1a8 (CTS2107)
- O2a1c1a1a9 (SK1691)
- O2a1c1a1a1 (F632)
- O2a1c1a1b (PH203)
- O2a1c1a1a (F11)
- O2a1c1a1 (F13)
- O2a1c1b (F449)
- O2a1c1b1 (F238)
- O2a1c1b1a (F134)
- O2a1c1b1a1 (F1273)
- O2a1c1b1a2 (F724)
- O2a1c1b1a (F134)
- O2a1c1b2 (F1266)
- O2a1c1b1 (F238)
- O2a1c1c (CTS498)
- O2a1c1a (F117)
- O2a1c2 (FGC3750/SK1673)
- O2a1c1 (F18)
- O2a1a (F1876/Page127)
- O2a2 (IMS-JST021354/P201)
- O2a2a (M188)
- O2a2a1 (F2588)
- O2a2a1a (CTS445)
- O2a2a1a1 (CTS201)
- O2a2a1a1a (M159/Page96)
- O2a2a1a2 (M7)
- O2a2a1a2a (F1276)
- O2a2a1a2a1 (CTS6489)
- O2a2a1a2a1a (F1275)
- O2a2a1a2a1a1 (M113)
- O2a2a1a2a1a2 (N5)
- O2a2a1a2a1a3 (Z25400)
- O2a2a1a2a1a (F1275)
- O2a2a1a2a2 (F1863)
- O2a2a1a2a2a (F1134)
- O2a2a1a2a2a1 (F1262)
- O2a2a1a2a2a (F1134)
- O2a2a1a2a1 (CTS6489)
- O2a2a1a2b (Y26403)
- O2a2a1a2a (F1276)
- O2a2a1a1 (CTS201)
- O2a2a1b (F1837)
- O2a2a1a (CTS445)
- O2a2a2 (F879)
- O2a2a2a (F1226)
- O2a2a2a1 (F2859)
- O2a2a2a (F1226)
- O2a2a1 (F2588)
- O2a2b (P164)
- O2a2b1 (M134)
- O2a2b1a (F450/M1667)
- O2a2b1a1 (M117/Page23)
- O2a2b1a1a (M133)
- O2a2b1a1a1 (F438)
- O2a2b1a1a1a (Y17728)
- O2a2b1a1a1a1 (F155)
- O2a2b1a1a1a1a (F813/M6539)
- O2a2b1a1a1a1a1 (Y20928)
- O2a2b1a1a1a1a (F813/M6539)
- O2a2b1a1a1a2 (F1754)
- O2a2b1a1a1a2a (F2137)
- O2a2b1a1a1a2a1 (F1442)
- O2a2b1a1a1a2a1a (F1123)
- O2a2b1a1a1a2a1a1 (F1369)
- O2a2b1a1a1a2a1a (F1123)
- O2a2b1a1a1a2a2 (A16636)
- O2a2b1a1a1a2a1 (F1442)
- O2a2b1a1a1a2a (F2137)
- O2a2b1a1a1a3 (Z25907)
- O2a2b1a1a1a1 (F155)
- O2a2b1a1a1a (Y17728)
- O2a2b1a1a2 (FGC23469/Z25852)
- O2a2b1a1a2a (F310)
- O2a2b1a1a2a1 (F402)
- O2a2b1a1a2a1a (F1531)
- O2a2b1a1a2a1 (F402)
- O2a2b1a1a2a (F310)
- O2a2b1a1a3 (CTS7634)
- O2a2b1a1a3a (F317)
- O2a2b1a1a3a1 (F3039)
- O2a2b1a1a3a2 (Y29861)
- O2a2b1a1a3b (CTS5488)
- O2a2b1a1a3a (F317)
- O2a2b1a1a4 (Z25853)
- O2a2b1a1a4a (CTS5492)
- O2a2b1a1a4a1 (CTS6987)
- O2a2b1a1a4a1a (Z42620)
- O2a2b1a1a4a2 ( F20963)
- O2a2b1a1a4a1 (CTS6987)
- O2a2b1a1a4a (CTS5492)
- O2a2b1a1a5 (CTS10738/M1707)
- O2a2b1a1a5a (CTS9678)
- O2a2b1a1a5a1 (Z39663)
- O2a2b1a1a5a2 (M1513)
- O2a2b1a1a5b (A9457)
- O2a2b1a1a5b1 (F17158)
- O2a2b1a1a5a (CTS9678)
- O2a2b1a1a6 (CTS4658)
- O2a2b1a1a6a (CTS5308)
- O2a2b1a1a6b (Z25928)
- O2a2b1a1a6b1 (SK1730/Z25982)
- O2a2b1a1a6b1a (Z26030)
- O2a2b1a1a6b1b (Z26010)
- O2a2b1a1a6b2 (A9462)
- O2a2b1a1a6b3 (B456)
- O2a2b1a1a6b1 (SK1730/Z25982)
- O2a2b1a1a7 (YP4864)
- O2a2b1a1a7a (Z44068)
- O2a2b1a1a7a1 (F5525/SK1748)
- O2a2b1a1a7b (Z44071)
- O2a2b1a1a7a (Z44068)
- O2a2b1a1a8 (Z44091)
- O2a2b1a1a8a (Z44092)
- O2a2b1a1a1 (F438)
- O2a2b1a1b (CTS4960)
- O2a2b1a1a (M133)
- O2a2b1a2 (F114)
- O2a2b1a2a (F79)
- O2a2b1a2a1 (F46/Y15)
- O2a2b1a2a1a (FGC16847/Z26091)
- O2a2b1a2a1a1 (F48)
- O2a2b1a2a1a1a (F152)
- O2a2b1a2a1a1a1 (F2505)
- O2a2b1a2a1a1b (CTS3149)
- O2a2b1a2a1a1a (F152)
- O2a2b1a2a1a2 (F242)
- O2a2b1a2a1a2a (CTS4266)
- O2a2b1a2a1a2a1 (Z26108)
- O2a2b1a2a1a2a1a (F2173)
- O2a2b1a2a1a2a1 (Z26108)
- O2a2b1a2a1a2a (CTS4266)
- O2a2b1a2a1a3 (F2887)
- O2a2b1a2a1a3a (F3607)
- O2a2b1a2a1a3a1 (F3525)
- O2a2b1a2a1a3b (CTS3763)
- O2a2b1a2a1a3b1 (A9472)
- O2a2b1a2a1a3b2 (FGC16863/Y7110)
- O2a2b1a2a1a3b2a (L1360)
- O2a2b1a2a1a3b2a1 (FGC16889)
- O2a2b1a2a1a3b2b (SK1768/Y7112/Z26257)
- O2a2b1a2a1a3b2b1 (F4249)
- O2a2b1a2a1a3b2b1a (FGC23868)
- O2a2b1a2a1a3b2b2 (CTS335)
- O2a2b1a2a1a3b2b1 (F4249)
- O2a2b1a2a1a3b2a (L1360)
- O2a2b1a2a1a3a (F3607)
- O2a2b1a2a1a1 (F48)
- O2a2b1a2a1b (CTS53)
- O2a2b1a2a1b1 (CTS6373)
- O2a2b1a2a1b1a (A9473)
- O2a2b1a2a1b1 (CTS6373)
- O2a2b1a2a1c (F3386)
- O2a2b1a2a1d (Y29828)
- O2a2b1a2a1d1 (F735)
- O2a2b1a2a1d1a (FGC34973)
- O2a2b1a2a1d1b (F1739)
- O2a2b1a2a1d1 (F735)
- O2a2b1a2a1a (FGC16847/Z26091)
- O2a2b1a2a1 (F46/Y15)
- O2a2b1a2b (F743)
- O2a2b1a2b1 (CTS8481)
- O2a2b1a2b1a (CTS4325)
- O2a2b1a2b1a1 (A16629)
- O2a2b1a2b1a2 (CTS682)
- O2a2b1a2b1a (CTS4325)
- O2a2b1a2b2 (F748)
- O2a2b1a2b2a (F728)
- O2a2b1a2b1 (CTS8481)
- O2a2b1a2c (Page101)
- O2a2b1a2a (F79)
- O2a2b1a1 (M117/Page23)
- O2a2b1a (F450/M1667)
- O2a2b2 (AM01822/F3223)
- O2a2b2a (AM01856/F871)
- O2a2b2a1 (N7)
- O2a2b2a1a (F4110)
- O2a2b2a1a1 (F4068)
- O2a2b2a1a2 (SK1780)
- O2a2b2a1b (F4124)
- O2a2b2a1b1 (IMS-JST008425p6)
- O2a2b2a1b2 (BY15188)
- O2a2b2a1b2a (F16411)
- O2a2b2a1a (F4110)
- O2a2b2a2 (AM01845/F706)
- O2a2b2a2a (F717)
- O2a2b2a2a1 (F3612)
- O2a2b2a2a2 (SK1783)
- O2a2b2a2b (AM01847/B451)
- O2a2b2a2b1 (A17418)
- O2a2b2a2b2 (AM01756)
- O2a2b2a2b2a (B450)
- O2a2b2a2b2b (AM00472/B452)
- O2a2b2a2b2b1 (F18942)
- O2a2b2a2b2c (A16427)
- O2a2b2a2a (F717)
- O2a2b2a1 (N7)
- O2a2b2b (A16433)
- O2a2b2b1 (A16438)
- O2a2b2b1a (SK1775)
- O2a2b2b1a1 (SK1774)
- O2a2b2b1b (A16440)
- O2a2b2b1a (SK1775)
- O2a2b2b1 (A16438)
- O2a2b2a (AM01856/F871)
- O2a2b1 (M134)
- O2a2a (M188)
- O2a3 (M300)
- O2a4 (M333)
- O2a1 (L127.1)
- O2b (F742)
- O2b1 (F1150)
- O2b1a (F837)
- O2b1a1 (F1025)
- O2b1a (F837)
- O2b2 (F1055)
- O2b2a (F3021)
- O2b1 (F1150)
- O2a (M324)
- O1 (F265/M1354, CTS2866, F75/M1297, F429/M1415, F465/M1422)
See also
editGenetics
editY-DNA O subclades
editY-DNA backbone tree
editNotes
editReferences
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- ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br bs bt bu bv bw bx by bz ca cb cc cd ce cf cg ch ci cj ck cl cm cn co cp cq cr cs ct cu cv cw cx cy cz da db dc dd de df dg dh di dj dk dl dm dn do dp dq dr ds dt du dv dw dx dy dz ea eb ec ed ee ef eg eh ei ej ek el em en eo ep eq er es et eu ev ew ex ey ez fa fb fc fd fe ff fg fh fi fj fk fl fm fn fo fp fq fr fs ft fu fv fw fx fy fz ga gb gc gd ge gf gg gh gi gj gk gl gm gn go gp gq gr gs gt gu gv gw gx gy gz ha hb hc hd he hf hg hh hi hj hk hl hm hn ho hp hq hr hs ht hu hv hw hx hy hz ia ib ic id ie if ig ih ii ij ik il im in io ip iq ir is it iu iv iw ix iy iz ja jb jc jd je jf jg jh ji jj jk jl jm jn jo jp jq jr js jt ju jv jw jx jy jz ka kb kc kd ke kf kg kh ki kj kk kl km kn ko kp kq kr ks kt ku kv kw kx ky kz la lb lc ld le lf lg lh li lj lk ll lm ln lo lp lq lr ls lt lu lv lw lx ly lz ma mb mc md me mf mg mh mi mj mk ml mm mn mo mp mq mr ms mt mu mv mw mx my mz na nb nc nd ne nf ng nh ni nj nk nl nm nn no np nq nr ns nt nu nv nw nx ny nz oa ob oc od oe of og oh oi oj ok ol om on oo op oq or os ot ou ov ow ox oy oz pa pb pc pd pe pf pg ph pi pj pk pl pm pn po pp pq pr ps pt pu pv pw px py pz qa qb qc qd qe qf qg qh qi qj qk YFull Haplogroup YTree v5.04 at 16 May 2017
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Sources for conversion tables
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Further reading
edit- Edmondson JA (2007). Jimmy G. Harris, Somsonge Burusphat and James E. Harris (ed.). "The power of language over the past: Tai settlement and Tai linguistics in southern China and northern Vietnam" (PDF). Studies in Southeast Asian Languages and Linguistics. Bangkok, Thailand: Ek Phim Thai Co. Ltd. Archived from the original (PDF) on 21 August 2007. Retrieved 24 October 2010.
- van Driem, George (2011). "Rice and the Austroasiatic and Hmong-Mien Homelands". In Enfield, N. J (ed.). Dynamics of Human Diversity (PDF). Pacific Linguistics. pp. 361–390. CiteSeerX 10.1.1.694.9991. ISBN 978-0-85883-638-9. S2CID 135246934. Archived from the original on 7 February 2016.
{{cite book}}
: CS1 maint: unfit URL (link) - Firasat S, Khaliq S, Mohyuddin A, Papaioannou M, Tyler-Smith C, Underhill PA, Ayub Q (January 2007). "Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan". European Journal of Human Genetics. 15 (1): 121–6. doi:10.1038/sj.ejhg.5201726. PMC 2588664. PMID 17047675.
- Fornarino, Simona; Pala, Maria; Battaglia, Vincenza; Maranta, Ramona; Achilli, Alessandro; Modiano, Guido; Torroni, Antonio; Semino, Ornella; Santachiara-Benerecetti, Silvana A (December 2009). "Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation". BMC Evolutionary Biology. 9 (1): 154. Bibcode:2009BMCEE...9..154F. doi:10.1186/1471-2148-9-154. PMC 2720951. PMID 19573232.
- Karafet TM, Mendez FL, Meilerman MB, Underhill PA, Zegura SL, Hammer MF (May 2008). "New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree". Genome Research. 18 (5): 830–8. doi:10.1101/gr.7172008. PMC 2336805. PMID 18385274.
- Kayser M, Choi Y, van Oven M, Mona S, Brauer S, Trent RJ, et al. (July 2008). "The impact of the Austronesian expansion: evidence from mtDNA and Y chromosome diversity in the Admiralty Islands of Melanesia". Molecular Biology and Evolution. 25 (7): 1362–74. doi:10.1093/molbev/msn078. PMID 18390477.
- Kharkov, V. N.; Stepanov, V. A.; Medvedeva, O. F.; Spiridonova, M. G.; Voevoda, M. I.; Tadinova, V. N.; Puzyrev, V. P. (2007). "Gene pool differences between Northern and Southern Altaians inferred from the data on Y-chromosomal haplogroups". Russian Journal of Genetics. 43 (5): 551–562. doi:10.1134/S1022795407050110. PMID 17633562. S2CID 566825.
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External links
edit- Bradshaw Foundation. "Journey of Man - The Peopling of the World".
- ISOGG (2012). "Y-DNA Haplogroup O and its Subclades - 2012".
- TMC (1998). "Genetic Findings Support 'Out of Africa' Theory". Archived from the original on 10 October 2009.
- Spread of Haplogroup O, from The Genographic Project, National Geographic
- Y-DNA Phylogenetic Tree of Haplogroup O (DNAHaplogroups.org)
- Migration patterns of early Humans and the full size map
- China DNA at Family Tree DNA