H-InvDB x AHG DB
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H-InvDB_9.0 released on May 27, 2015.
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H-Invitational ID: HIT000338997 Accession number: BC108255 Created date: 26-Mar-2013 Last modified: 27-May-2015
Definition: TFIIH basal transcription factor complex helicase XPD subunit; EC=3.6.4.12; Basic transcription factor 2 80 kDa subunit; BTF2 p80; CXPD; DNA excision repair protein ERCC-2; DNA repair protein complementing XP-D cells; TFIIH basal transcription factor complex 80 kDa subunit; TFIIH 80 kDa subunit; TFIIH p80; Xeroderma pigmentosum group D-complementing protein;
 
 

Disease/pathology information  DiseaseInfo Viewer LEGENDA Last modified:27-May-2015
Disease relation Disease name: Cerebrooculofacioskeletal syndrome 2 (610756);  Disease name: Trichothiodystrophy (601675);  Disease name: Xeroderma pigmentosum, group D (278730); 
Related information in OMIM OMIM ID:  126340;  Title: EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 2
Co-localized orphan diseases NA
Disease related mutation MutationView:  126340
JRE-1.4.0 or later is required.Download JRE at Sun's web site.
Literature-Extracted GENe-Disease Associations (LEGENDA) LEGENDA Gene name Entrez Gene ID:(2068)
Disease Entrez Gene ID:(2068)
Substance Entrez Gene ID:(2068)
Related H-InvDB links DiseaseInfo ViewerDiseaseInfo ViewerLEGENDALEGENDA