Sequence of THG1_HUMAN

tRNAHis guanylyltransferase

Q9NWX6

298

34831

366933

Guo D.,Hu K.,Lei Y.,Wang Y.,Ma T.,He D.

Identification and characterization of a novel cytoplasm protein ICF45 that is involved in cell cycle regulation.

J. Biol. Chem.

279

53498-53505

2004

366934

Wiemann S.,Weil B.,Wellenreuther R.,Gassenhuber J.,Glassl S.,Ansorge W.,Boecher M.,Bloecker H.,Bauersachs S.,Blum H.,Lauber J.,Duesterhoeft A.,Beyer A.,Koehrer K.,Strack N.,Mewes H.-W.,Ottenwaelder B.,Obermaier B.,Tampe J.,Heubner D.,Wambutt R.,Korn B.,Klein M.,Poustka A.

Towards a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.

Genome Res.

11

422-435

2001

366935

Ota T.,Suzuki Y.,Nishikawa T.,Otsuki T.,Sugiyama T.,Irie R.,Wakamatsu A.,Hayashi K.,Sato H.,Nagai K.,Kimura K.,Makita H.,Sekine M.,Obayashi M.,Nishi T.,Shibahara T.,Tanaka T.,Ishii S.,Yamamoto J.,Saito K.,Kawai Y.,Isono Y.,Nakamura Y.,Nagahari K.,Murakami K.,Yasuda T.,Iwayanagi T.,Wagatsuma M.,Shiratori A.,Sudo H.,Hosoiri T.,Kaku Y.,Kodaira H.,Kondo H.,Sugawara M.,Takahashi M.,Kanda K.,Yokoi T.,Furuya T.,Kikkawa E.,Omura Y.,Abe K.,Kamihara K.,Katsuta N.,Sato K.,Tanikawa M.,Yamazaki M.,Ninomiya K.,Ishibashi T.,Yamashita H.,Murakawa K.,Fujimori K.,Tanai H.,Kimata M.,Watanabe M.,Hiraoka S.,Chiba Y.,Ishida S.,Ono Y.,Takiguchi S.,Watanabe S.,Yosida M.,Hotuta T.,Kusano J.,Kanehori K.,Takahashi-Fujii A.,Hara H.,Tanase T.-O.,Nomura Y.,Togiya S.,Komai F.,Hara R.,Takeuchi K.,Arita M.,Imose N.,Musashino K.,Yuuki H.,Oshima A.,Sasaki N.,Aotsuka S.,Yoshikawa Y.,Matsunawa H.,Ichihara T.,Shiohata N.,Sano S.,Moriya S.,Momiyama H.,Satoh N.,Takami S.,Terashima Y.,Suzuki O.,Nakagawa S.,Senoh A.,Mizoguchi H.,Goto Y.,Shimizu F.,Wakebe H.,Hishigaki H.,Watanabe T.,Sugiyama A.,Takemoto M.,Kawakami B.,Yamazaki M.,Watanabe K.,Kumagai A.,Itakura S.,Fukuzumi Y.,Fujimori Y.,Komiyama M.,Tashiro H.,Tanigami A.,Fujiwara T.,Ono T.,Yamada K.,Fujii Y.,Ozaki K.,Hirao M.,Ohmori Y.,Kawabata A.,Hikiji T.,Kobatake N.,Inagaki H.,Ikema Y.,Okamoto S.,Okitani R.,Kawakami T.,Noguchi S.,Itoh T.,Shigeta K.,Senba T.,Matsumura K.,Nakajima Y.,Mizuno T.,Morinaga M.,Sasaki M.,Togashi T.,Oyama M.,Hata H.,Watanabe M.,Komatsu T.,Mizushima-Sugano J.,Satoh T.,Shirai Y.,Takahashi Y.,Nakagawa K.,Okumura K.,Nagase T.,Nomura N.,Kikuchi H.,Masuho Y.,Yamashita R.,Nakai K.,Yada T.,Nakamura Y.,Ohara O.,Isogai T.,Sugano S.

Complete sequencing and characterization of 21,243 full-length human cDNAs.

Nat. Genet.

36

40-45

2004

366939

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

Genome Res.

14

2121-2127

2004

366940

Hickey F.B.,Corcoran J.B.,Griffin B.,Bhreathnach U.,Mortiboys H.,Reid H.M.,Andrews D.,Byrne S.,Furlong F.,Martin F.,Godson C.,Murphy M.

IHG-1 increases mitochondrial fusion and bioenergetic function.

Diabetes

63

4314-4325

2014

366941

Hyde S.J.,Eckenroth B.E.,Smith B.A.,Eberley W.A.,Heintz N.H.,Jackman J.E.,Doublie S.

tRNA(His) guanylyltransferase (THG1), a unique 3'-5' nucleotidyl transferase, shares unexpected structural homology with canonical 5'-3' DNA polymerases.

Proc. Natl. Acad. Sci. U.S.A.

107

20305-20310

2010

366942

Edvardson S.,Elbaz-Alon Y.,Jalas C.,Matlock A.,Patel K.,Labbe K.,Shaag A.,Jackman J.E.,Elpeleg O.

A mutation in the THG1L gene in a family with cerebellar ataxia and developmental delay.

Neurogenetics

17

219-225

2016

366943

Walker M.A.,Lerman-Sagie T.,Swoboda K.,Lev D.,Blumkin L.

Refining the phenotype of the THG1L (p.Val55Ala mutation)-related mitochondrial autosomal recessive congenital cerebellar ataxia.

Am. J. Med. Genet. A

179

1575-1579

2019

366944

Shaheen R.,Maddirevula S.,Ewida N.,Alsahli S.,Abdel-Salam G.M.H.,Zaki M.S.,Tala S.A.,Alhashem A.,Softah A.,Al-Owain M.,Alazami A.M.,Abadel B.,Patel N.,Al-Sheddi T.,Alomar R.,Alobeid E.,Ibrahim N.,Hashem M.,Abdulwahab F.,Hamad M.,Tabarki B.,Alwadei A.H.,Alhazzani F.,Bashiri F.A.,Kentab A.,Sahintuerk S.,Sherr E.,Fregeau B.,Sogati S.,Alshahwan S.A.M.,Alkhalifi S.,Alhumaidi Z.,Temtamy S.,Aglan M.,Otaify G.,Girisha K.M.,Tulbah M.,Seidahmed M.Z.,Salih M.A.,Abouelhoda M.,Momin A.A.,Saffar M.A.,Partlow J.N.,Arold S.T.,Faqeih E.,Walsh C.,Alkuraya F.S.

Genomic and phenotypic delineation of congenital microcephaly.

Genet. Med.

21

545-552

2019