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rdfs:label
Haplogrupo H (ADNmt) ハプログループH (mtDNA) Haplogruppe H (mtDNA) Haplogrupo H (ADNmt) Haplogroupe H (ADNmt) Haploskupina H (mtDNA) Гаплогруппа H (мтДНК) Haplogroup H (mtDNA)
rdfs:comment
ハプログループH (mtDNA)は分子人類学におけるミトコンドリアDNAハプログループの一タイプであり、ハプログループHVの子型のうち「G2706A, T7028C」で定義されるもの。西南アジアにおいて、25000-20000年前に誕生したと考えられている。ヒトミトコンドリアDNAの参照配列として用いられているケンブリッジ参照配列は、このハプログループ(詳細にはH2a2a1)に属している。 Em genética humana, o haplogrupo H (ADNmt) é um haplogrupo do ADN mitocondrial humano (ADNmt) tipico da Euroasia ocidental. Deriva do haplogrupo HV (ADNmt) e constitui o haplogrupo mais carateristico em todo o continente europeu, exceto entre os lapões. como pode ser observado seguindo a hiper-ligação. Die Haplogruppe H ist in der Humangenetik eine Haplogruppe der Mitochondrien. Die (CRS), die mitochondriale Sequenz, mit der alle anderen Sequenzen verglichen werden, gehört zu Haplogruppe H. Haplogruppe H ist mit 40 % bis 50 % die häufigste mtDNA Haplogruppe in Europa. Diese Haplogruppe ist auch in Nordafrika und dem Nahen Osten verbreitet. Diese Dichte sinkt im Südosten des Kontinents auf 20 % im Nahen Osten sowie im Kaukasus. Nach FamilyTreeDNA steht die Nucleotid-Position 4336 tRNA-Variante der Haplogruppe H im Zusammenhang mit dem späteren Beginn der Alzheimer-Krankheit. L'haplogroupe H est un haplogroupe du génome mitochondrial humain (ADNmt). Il est particulièrement répandu en Europe, où 40 % des habitants seraient de cet haplogroupe, mais on le trouve aussi tout autour de la Méditerranée et dans le Caucase, avec des poussées vers l'Afrique de l'Est et vers l'Asie centrale. Il existe différents sous-clades de H. Haploskupina H je haploskupina lidské mitochondriální DNA. Z haploskupiny H vychází Cambridžská referenční sekvence (CRS), vůči které jsou porovnávány veškeré jiné sekvence mitochondriální DNA. Přibližně polovina Evropanů je nositeli haploskupiny H. Tato haploskupina je dále běžná v Severní Africe a na Blízkém Východě. FamilyTreeDNA, v současnosti největší laboratoř zabývající se genealogickými testy DNA, má ve své databázi přibližně 32 % vzorků, které patří haploskupině H. Z nich má přibližně 21 % mutaci 519C, která je nestálá a tudíž ji nelze využít pro zatřídění vzorků do dalších podskupin. Změna nukleotidu tRNA na pozici 4336 je u haploskupiny H spojována s nástupem Alzheimerovy choroby. En genética humana el haplogrupo H es un linaje mitocondrial humano (ADNmt) típico de Eurasia Occidental. Es derivado del haplogrupo HV y es el haplogrupo matrilineal más característico de toda Europa (excepto en los sami), predominando en Europa Occidental. Гаплогруппа H — гаплогруппа митохондриальной ДНК человека. Является потомком гаплогруппы HV. «Кембриджская эталонная последовательность» — человеческая митохондриальная последовательность, с которой сравниваются все прочие, принадлежит гаплогруппе H. Haplogroup H is a human mitochondrial DNA (mtDNA) haplogroup. The clade is believed to have originated in Southwest Asia, near present day Syria, around 20,000 to 25,000 years ago. Mitochondrial haplogroup H is today predominantly found in Europe, and is believed to have evolved before the Last Glacial Maximum (LGM). It first expanded in the northern Near East and Southern Caucasus soon, and later migrations from Iberia suggest that the clade reached Europe before the Last Glacial Maximum. The haplogroup has also spread to parts of Africa, Siberia and inner Asia. Today, around 40% of all maternal lineages in Europe belong to haplogroup H.
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H
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dbo:abstract
L'haplogroupe H est un haplogroupe du génome mitochondrial humain (ADNmt). Il est particulièrement répandu en Europe, où 40 % des habitants seraient de cet haplogroupe, mais on le trouve aussi tout autour de la Méditerranée et dans le Caucase, avec des poussées vers l'Afrique de l'Est et vers l'Asie centrale. Il existe différents sous-clades de H. Гаплогруппа H — гаплогруппа митохондриальной ДНК человека. Является потомком гаплогруппы HV. «Кембриджская эталонная последовательность» — человеческая митохондриальная последовательность, с которой сравниваются все прочие, принадлежит гаплогруппе H. Haplogroup H is a human mitochondrial DNA (mtDNA) haplogroup. The clade is believed to have originated in Southwest Asia, near present day Syria, around 20,000 to 25,000 years ago. Mitochondrial haplogroup H is today predominantly found in Europe, and is believed to have evolved before the Last Glacial Maximum (LGM). It first expanded in the northern Near East and Southern Caucasus soon, and later migrations from Iberia suggest that the clade reached Europe before the Last Glacial Maximum. The haplogroup has also spread to parts of Africa, Siberia and inner Asia. Today, around 40% of all maternal lineages in Europe belong to haplogroup H. Em genética humana, o haplogrupo H (ADNmt) é um haplogrupo do ADN mitocondrial humano (ADNmt) tipico da Euroasia ocidental. Deriva do haplogrupo HV (ADNmt) e constitui o haplogrupo mais carateristico em todo o continente europeu, exceto entre os lapões. como pode ser observado seguindo a hiper-ligação. Haploskupina H je haploskupina lidské mitochondriální DNA. Z haploskupiny H vychází Cambridžská referenční sekvence (CRS), vůči které jsou porovnávány veškeré jiné sekvence mitochondriální DNA. Přibližně polovina Evropanů je nositeli haploskupiny H. Tato haploskupina je dále běžná v Severní Africe a na Blízkém Východě. FamilyTreeDNA, v současnosti největší laboratoř zabývající se genealogickými testy DNA, má ve své databázi přibližně 32 % vzorků, které patří haploskupině H. Z nich má přibližně 21 % mutaci 519C, která je nestálá a tudíž ji nelze využít pro zatřídění vzorků do dalších podskupin. Změna nukleotidu tRNA na pozici 4336 je u haploskupiny H spojována s nástupem Alzheimerovy choroby. Bryan Sykes použil ve své knize Sedm dcer Eviných pro zakladatelku haploskupiny H jméno Helena. Die Haplogruppe H ist in der Humangenetik eine Haplogruppe der Mitochondrien. Die (CRS), die mitochondriale Sequenz, mit der alle anderen Sequenzen verglichen werden, gehört zu Haplogruppe H. Haplogruppe H ist mit 40 % bis 50 % die häufigste mtDNA Haplogruppe in Europa. Diese Haplogruppe ist auch in Nordafrika und dem Nahen Osten verbreitet. Diese Dichte sinkt im Südosten des Kontinents auf 20 % im Nahen Osten sowie im Kaukasus. Nach FamilyTreeDNA steht die Nucleotid-Position 4336 tRNA-Variante der Haplogruppe H im Zusammenhang mit dem späteren Beginn der Alzheimer-Krankheit. Im Buch Die sieben Töchter Evas von Bryan Sykes ist die Urmutter dieser Haplogruppe Helena. ハプログループH (mtDNA)は分子人類学におけるミトコンドリアDNAハプログループの一タイプであり、ハプログループHVの子型のうち「G2706A, T7028C」で定義されるもの。西南アジアにおいて、25000-20000年前に誕生したと考えられている。ヒトミトコンドリアDNAの参照配列として用いられているケンブリッジ参照配列は、このハプログループ(詳細にはH2a2a1)に属している。 En genética humana el haplogrupo H es un linaje mitocondrial humano (ADNmt) típico de Eurasia Occidental. Es derivado del haplogrupo HV y es el haplogrupo matrilineal más característico de toda Europa (excepto en los sami), predominando en Europa Occidental.
dbp:ancestor
dbr:Haplogroup_HV_(mtDNA)
dbp:descendants
H* lineages; subclades H1, H2, H3, H4, H5'36, H6, H7, H8, H9, H10, H11, H12, H13, H14, H15, H16, H18, H19, H20, H22, H23, H24, H25, H26, H28, H29, H31, H32, H33, H34, H35, H37, H38, H39, 16129, 16129
dbp:mutations
G2706A, T7028C
dbp:originPlace
dbr:Lesser_Caucasus dbr:West_Asia
gold:hypernym
dbr:Haplogroup
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wikipedia-en:Haplogroup_H_(mtDNA)?oldid=1124102844&ns=0
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