Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10915
Gene name Gene Name - the full gene name approved by the HGNC.
Transcription elongation regulator 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TCERG1
Synonyms (NCBI Gene) Gene synonyms aliases
CA150, TAF2S, Urn1
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5q32
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a nuclear protein that regulates transcriptional elongation and pre-mRNA splicing. The encoded protein interacts with the hyperphosphorylated C-terminal domain of RNA polymerase II via multiple FF domains, and with the pre-mRNA splicing
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT027828 hsa-miR-98-5p Microarray 19088304
MIRT052589 hsa-let-7a-5p CLASH 23622248
MIRT046720 hsa-miR-222-3p CLASH 23622248
MIRT043747 hsa-miR-328-3p CLASH 23622248
MIRT040393 hsa-miR-615-3p CLASH 23622248
Transcription factors
Transcription factor Regulation Reference
SF1 Repression 11604498
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 IDA 20956529
GO:0001103 Function RNA polymerase II repressing transcription factor binding IPI 20956529
GO:0003711 Function Transcription elongation regulator activity TAS 20215116
GO:0003712 Function Transcription coregulator activity IBA 21873635
GO:0003713 Function Transcription coactivator activity TAS 9315662
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605409 15630 ENSG00000113649
Protein
UniProt ID O14776
Protein name Transcription elongation regulator 1 (TATA box-binding protein-associated factor 2S) (Transcription factor CA150)
Protein function Transcription factor that binds RNA polymerase II and inhibits the elongation of transcripts from target promoters. Regulates transcription elongation in a TATA box-dependent manner. Necessary for TAT-dependent activation of the human immunodefi
PDB 2DK7 , 2DOD , 2DOE , 2DOF , 2E71 , 2KIQ , 2KIS , 2MW9 , 2MWA , 2MWB , 2MWD , 2MWE , 2MWF , 2N4R , 2N4S , 2N4T , 2N4U , 2N4V , 2N4W , 2NNT , 3HFH , 3Q1I , 4FQG , 7ABF , 7ABG , 8Q7N , 8QO9
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00397 WW 134 162 WW domain Domain
PF00397 WW 432 460 WW domain Domain
PF01846 FF 661 709 FF domain Family
PF01846 FF 727 776 FF domain Family
PF01846 FF 794 843 FF domain Family
PF01846 FF 898 949 FF domain Family
PF01846 FF 956 1007 FF domain Family
PF01846 FF 1014 1074 FF domain Family
Tissue specificity TISSUE SPECIFICITY: Detected in brain neurons. {ECO:0000269|PubMed:11172033}.
Sequence
MAERGGDGGESERFNPGELRMAQQQALRFRGPAPPPNAVMRGPPPLMRPPPPFGMMRGPP
PPPRPPFGRPPFDPNMPPMPPPGGIPPPMGPPHLQRPPFMPPPMSSMPPPPGMMFPPGMP
PVTAPGTPALPPTEEIWVENKTPDGKVYYYNARTRESAWTKPDGVKVIQQSELTPMLAAQ
AQVQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQAQ
AQVQAQVQAQVQAQAVGASTPTTSSPAPAVSTSTSSSTPSSTTSTTTTATSVAQTVSTPT
TQDQTPSSAVSVATPTVSVSTPAPTATPVQTVPQPHPQTLPPAVPHSVPQPTTAIPAFPP
VMVPPFRVPLPGMPIPLPGVAMMQIVSCPYVKTVATTKTGVLPGMAPPIVPMIHPQVAIA
ASPATLAGATAVSEWTEYKTADGKTYYYNNRTLESTWEKPQELKEKEKLEEKIKEPIKEP
SEEPLPMETEEEDPKEEPIKEIKEEPKEEEMTEEEKAAQKAKPVATAPIPGTPWCVVWTG
DERVFFYNPTTRLSMWDRPDDLIGRADVDKIIQEPPHKKGMEELKKLRHPTPTMLSIQKW
QFSMSAIKEEQELMEEINEDEPVKAKKRKRDDNKDIDSEKEAAMEAEIKAARERAIVPLE
ARMKQFKDMLLERGVSAFSTWEKELHKIVFDPRYLLLNPKERKQVFDQYVKTRAEEERRE
KKNKIMQAKEDFKKMMEEAKFNPRATFSEFAAKHAKDSRFKAIEKMKDREALFNEFVAAA
RKKEKEDSKTRGEKIKSDFFELLSNHHLDSQSRWSKVKDKVESDPRYKAVDSSSMREDLF
KQY
IEKIAKNLDSEKEKELERQARIEASLREREREVQKARSEQTKEIDREREQHKREEAI
QNFKALLSDMVRSSDVSWSDTRRTLRKDHRWESGSLLEREEKEKLFNEH
IEALTKKKREH
FRQLLDETSAITLTSTWKEVKKIIKEDPRCIKFSSSDRKKQREFEEY
IRDKYITAKADFR
TLLKETKFITYRSKKLIQESDQHLKDVEKILQNDKRYLVLDCVPEERRKLIVAY
VDDLDR
RGPPPPPTASEPTRRSTK
Sequence length 1098
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Spliceosome  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Narcolepsy Narcolepsy rs104894574, rs387906655 19629137
Unknown
Disease term Disease name Evidence References Source
Rheumatoid arthritis Rheumatoid arthritis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Delayed Cranial Ossification due to CBFB Haploinsufficiency Associate 35617825
Huntington Disease Associate 17018562
Multiple Sclerosis Associate 31805175