Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6872
Gene name Gene Name - the full gene name approved by the HGNC.
TATA-box binding protein associated factor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TAF1
Synonyms (NCBI Gene) Gene synonyms aliases
BA2R, CCG1, CCGS, DYT3, DYT3/TAF1, KAT4, MRXS33, N-TAF1, NSCL2, OF, P250, TAF(II)250, TAF2A, TAFII-250, TAFII250, XDP
Disease Acronyms (UniProt) Disease acronyms from UniProt database
DYT3, MRXS33
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xq13.1
Summary Summary of gene provided in NCBI Entrez Gene.
Initiation of transcription by RNA polymerase II requires the activities of more than 70 polypeptides. The protein that coordinates these activities is the basal transcription factor TFIID, which binds to the core promoter to position the polymerase prope
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs144106353 T>C Conflicting-interpretations-of-pathogenicity 5 prime UTR variant, genic upstream transcript variant, coding sequence variant, non coding transcript variant, synonymous variant
rs148448660 G>A Conflicting-interpretations-of-pathogenicity 5 prime UTR variant, missense variant, genic upstream transcript variant, non coding transcript variant, coding sequence variant
rs397509359 C>A,T Pathogenic Non coding transcript variant, genic downstream transcript variant
rs767354861 C>T Likely-pathogenic Coding sequence variant, genic upstream transcript variant, non coding transcript variant, missense variant
rs864321627 T>C Pathogenic Genic upstream transcript variant, genic downstream transcript variant, non coding transcript variant, missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018059 hsa-miR-335-5p Microarray 18185580
MIRT025847 hsa-miR-7-5p Microarray 17612493
MIRT030916 hsa-miR-21-5p Microarray 18591254
MIRT673006 hsa-miR-4486 HITS-CLIP 23824327
MIRT673004 hsa-miR-24-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IMP 24289924
GO:0000209 Process Protein polyubiquitination IDA 20181722
GO:0000785 Component Chromatin IDA 20181722, 24289924
GO:0000979 Function RNA polymerase II core promoter sequence-specific DNA binding IMP 25412659
GO:0001181 Function RNA polymerase I general transcription initiation factor activity IDA 12498690
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
313650 11535 ENSG00000147133
Protein
UniProt ID P21675
Protein name Transcription initiation factor TFIID subunit 1 (EC 2.3.1.48) (EC 2.7.11.1) (Cell cycle gene 1 protein) (TBP-associated factor 250 kDa) (p250) (Transcription initiation factor TFIID 250 kDa subunit) (TAF(II)250) (TAFII-250) (TAFII250)
Protein function The TFIID basal transcription factor complex plays a major role in the initiation of RNA polymerase II (Pol II)-dependent transcription (PubMed:33795473). TFIID recognizes and binds promoters with or without a TATA box via its subunit TBP, a TAT
PDB 1EQF , 3AAD , 3UV4 , 3UV5 , 4RGW , 4YYM , 4YYN , 5FUR , 5I1Q , 5I29 , 5MG2 , 6BQD , 6FIC , 6MZD , 6MZL , 6MZM , 6P38 , 6P39 , 6P3A , 7EDX , 7EG7 , 7EG8 , 7EG9 , 7EGA , 7EGB , 7EGC , 7EGD , 7EGE , 7EGH , 7EGI , 7EGJ , 7ENA , 7ENC , 7JJG , 7JJH , 7JSP , 7JTC , 7K03 , 7K0D , 7K0U , 7K1P , 7K27 , 7K3O , 7K42 , 7K6F , 7L6X , 7LB0 , 7LB1 , 7LB2 , 7LB3 , 7N42
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09247 TBP-binding 24 86 TATA box-binding protein binding Domain
PF12157 DUF3591 565 1028 Protein of unknown function (DUF3591) Family
PF15288 zf-CCHC_6 1261 1300 Zinc knuckle Domain
PF00439 Bromodomain 1389 1472 Bromodomain Domain
PF00439 Bromodomain 1511 1595 Bromodomain Domain
Sequence
MGPGCDLLLRTAATITAAAIMSDTDSDEDSAGGGPFSLAGFLFGNINGAGQLEGESVLDD
ECKKHLAGLGALGLGSLITELTANEE
LTGTDGALVNDEGWVRSTEDAVDYSDINEVAEDE
SRRYQQTMGSLQPLCHSDYDEDDYDADCEDIDCKLMPPPPPPPGPMKKDKDQDSITGEKV
DFSSSSDSESEMGPQEATQAESEDGKLTLPLAGIMQHDATKLLPSVTELFPEFRPGKVLR
FLRLFGPGKNVPSVWRSARRKRKKKHRELIQEEQIQEVECSVESEVSQKSLWNYDYAPPP
PPEQCLSDDEITMMAPVESKFSQSTGDIDKVTDTKPRVAEWRYGPARLWYDMLGVPEDGS
GFDYGFKLRKTEHEPVIKSRMIEEFRKLEENNGTDLLADENFLMVTQLHWEDDIIWDGED
VKHKGTKPQRASLAGWLPSSMTRNAMAYNVQQGFAATLDDDKPWYSIFPIDNEDLVYGRW
EDNIIWDAQAMPRLLEPPVLTLDPNDENLILEIPDEKEEATSNSPSKESKKESSLKKSRI
LLGKTGVIKEEPQQNMSQPEVKDPWNLSNDEYYYPKQQGLRGTFGGNIIQHSIPAVELRQ
PFFPTHMGPIKLRQFHRPPLKKYSFGALSQPGPHSVQPLLKHIKKKAKMREQERQASGGG
EMFFMRTPQDLTGKDGDLILAEYSEENGPLMMQVGMATKIKNYYKRKPGKDPGAPDCKYG
ETVYCHTSPFLGSLHPGQLLQAFENNLFRAPIYLHKMPETDFLIIRTRQGYYIRELVDIF
VVGQQCPLFEVPGPNSKRANTHIRDFLQVFIYRLFWKSKDRPRRIRMEDIKKAFPSHSES
SIRKRLKLCADFKRTGMDSNWWVLKSDFRLPTEEEIRAMVSPEQCCAYYSMIAAEQRLKD
AGYGEKSFFAPEEENEEDFQMKIDDEVRTAPWNTTRAFIAAMKGKCLLEVTGVADPTGCG
EGFSYVKIPNKPTQQKDDKEPQPVKKTVTGTDADLRRLSLKNAKQLLRKFGVPEEEIKKL
SRWEVIDV
VRTMSTEQARSGEGPMSKFARGSRFSVAEHQERYKEECQRIFDLQNKVLSST
EVLSTDTDSSSAEDSDFEEMGKNIENMLQNKKTSSQLSREREEQERKELQRMLLAAGSAA
SGNNHRDDDTASVTSLNSSATGRCLKIYRTFRDEEGKEYVRCETVRKPAVIDAYVRIRTT
KDEEFIRKFALFDEQHREEMRKERRRIQEQLRRLKRNQEKEKLKGPPEKKPKKMKERPDL
KLKCGACGAIGHMRTNKFCPLYYQTNAPPSNPVAMTEEQEEELEKTVIHNDNEELIKVEG
TKIVLGKQLIESADEVRRKSLVLKFPKQQLPPKKKRRVGTTVHCDYLNRPHKSIHRRRTD
PMVTLSSILESIINDMRDLPNTYPFHTPVNAKVVKDYYKIITRPMDLQTLRENVRKRLYP
SREEFREHLELIVKNSATYNGPKHSLTQISQS
MLDLCDEKLKEKEDKLARLEKAINPLLD
DDDQVAFSFILDNIVTQKMMAVPDSWPFHHPVNKKFVPDYYKVIVNPMDLETIRKNISKH
KYQSRESFLDDVNLILANSVKYNGPESQYTKTAQE
IVNVCYQTLTEYDEHLTQLEKDICT
AKEAALEEAELESLDPMTPGPYTPQPPDLYDTNTSLSMSRDASVFQDESNMSVLDIPSAT
PEKQVTQEGEDGDGDLADEEEGTVQQPQASVLYEDLLMSEGEDDEEDAGSDEEGDNPFSA
IQLSESGSDSDVGSGGIRPKQPRMLQENTRMDMENEESMMSYEGDGGEASHGLEDSNISY
GSYEEPDPKSNTQDTSFSSIGGYEVSEEEEDEEEEEQRSGPSVLSQVHLSEDEEDSEDFH
SIAGDSDLDSDE
Sequence length 1872
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Basal transcription factors   RNA Polymerase II Pre-transcription Events
Regulation of TP53 Activity through Phosphorylation
RNA Polymerase II Promoter Escape
RNA Polymerase II Transcription Pre-Initiation And Promoter Opening
RNA Polymerase II Transcription Initiation
RNA Polymerase II Transcription Initiation And Promoter Clearance
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Aplasia cutis congenita Aplasia Cutis Congenita rs587777706
Autism Autistic behavior rs121964908, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699
View all (8 more)
Colorectal cancer Adenocarcinoma of large intestine rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Developmental delay Global developmental delay, Gross motor development delay rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291
View all (32 more)
26350204
Unknown
Disease term Disease name Evidence References Source
Dystonia-parkinsonism, x-linked X-linked dystonia-parkinsonism ClinVar
Otitis media Chronic otitis media ClinVar
Intellectual Disability-Global Development Delay-Facial Dysmorphism-Sacral Caudal Remnant Syndrome, X-Linked X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome GenCC
Associations from Text Mining
Disease Name Relationship Type References
Blood Coagulation Disorders Associate 39252244
Carcinogenesis Associate 27571988
Carcinoma Hepatocellular Associate 30249878
Charcot Marie Tooth disease Type 2B Associate 7912286
Colitis Ulcerative Associate 39252244
Colorectal Neoplasms Associate 27571988, 35880088
Diabetes Mellitus Type 2 Associate 27906902
Dubowitz syndrome Associate 33098347
Dystonia Associate 16366515, 20200153, 31523486, 38042508
Dystonia 3 Torsion X Linked Associate 12928496, 1550125, 16366515, 20200153, 25604858, 26769797, 26879577, 28017799, 29229810, 29474915, 29474918, 32975318, 33315879, 35052466, 35216353
View all (6 more)