Gene Gene information from NCBI Gene database.
Entrez ID 10915
Gene name Transcription elongation regulator 1
Gene symbol TCERG1
Synonyms (NCBI Gene)
CA150TAF2SUrn1
Chromosome 5
Chromosome location 5q32
Summary 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.
175
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 factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
SF1 Repression 11604498
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
24
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IDA 20956529
GO:0003711 Function Transcription elongation factor activity TAS 20215116
GO:0003712 Function Transcription coregulator activity IBA
GO:0003713 Function Transcription coactivator activity TAS 9315662
GO:0003714 Function Transcription corepressor activity IDA 20956529
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605409 15630 ENSG00000113649
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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 associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Colorectal cancer Pathogenic rs1762720125 RCV001293848
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Delayed Cranial Ossification due to CBFB Haploinsufficiency Associate 35617825
Huntington Disease Associate 17018562
Multiple Sclerosis Associate 31805175