RecName: Full=Transcription initiation factor TFIID subunit 8; AltName - Protein

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Mutations in TAF8 cause a neurodegenerative disorder. [Brain. 2022]
Mutations in TAF8 cause a neurodegenerative disorder.
Wong KM, Jepsen WM, Efthymiou S, Salpietro V, Sanchez-Castillo M, Yip J, Kriouile Y, Diegmann S, Dreha-Kulaczewski S, Altmüller J, et al. Brain. 2022 Sep 14; 145(9):3022-3034.
Genomics and transcription analysis of human TFIID. [Oncogene. 1998]
Genomics and transcription analysis of human TFIID.
Purrello M, Di Pietro C, Viola A, Rapisarda A, Stevens S, Guermah M, Tao Y, Bonaiuto C, Arcidiacono A, Messina A, et al. Oncogene. 1998 Mar 26; 16(12):1633-8.
Homozygous TAF8 mutation in a patient with intellectual disability results in undetectable TAF8 protein, but preserved RNA polymerase II transcription. [Hum Mol Genet. 2018]
Homozygous TAF8 mutation in a patient with intellectual disability results in undetectable TAF8 protein, but preserved RNA polymerase II transcription.
El-Saafin F, Curry C, Ye T, Garnier JM, Kolb-Cheynel I, Stierle M, Downer NL, Dixon MP, Negroni L, Berger I, et al. Hum Mol Genet. 2018 Jun 15; 27(12):2171-2186.

RefSeq protein isoforms
See 17 reference sequence protein isoforms for the TAF8 gene.

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Q7Z7C8 [Domain Mapping of Disease Mut...]
Q7Z7C8
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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Reactome
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RecName: Full=Transcription initiation factor TFIID subunit 8; AltName: Full=Pro...
RecName: Full=Transcription initiation factor TFIID subunit 8; AltName: Full=Protein taube nuss; AltName: Full=TBP-associated factor 43 kDa; AltName: Full=TBP-associated factor 8; AltName: Full=Transcription initiation factor TFIID 43 kDa subunit; Short=TAFII-43; Short=TAFII43; Short=hTAFII43
gi|74723384|sp|Q7Z7C8.1|TAF8_HUMAN

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