Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
341032
Gene name Gene Name - the full gene name approved by the HGNC.
POU class 2 homeobox associating factor 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
POU2AF2
Synonyms (NCBI Gene) Gene synonyms aliases
C11orf53, OCA-T1, OCAT1
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q23.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT829969 hsa-miR-1228 CLIP-seq
MIRT829970 hsa-miR-1587 CLIP-seq
MIRT829971 hsa-miR-1910 CLIP-seq
MIRT829972 hsa-miR-3140-5p CLIP-seq
MIRT829973 hsa-miR-329 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0003713 Function Transcription coactivator activity IBA
GO:0003713 Function Transcription coactivator activity IDA 35576971
GO:0005515 Function Protein binding IPI 35576971
GO:0005634 Component Nucleus IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620671 30527 ENSG00000150750
Protein
UniProt ID Q8IXP5
Protein name POU domain class 2-associating factor 2 (Oct coactivator from tuft cells 1) (Protein OCA-T1) (POU class 2 homeobox-associating factor 2)
Protein function Transcriptional coactivator of POU2F3 (PubMed:35576971, PubMed:36197978). This complex drives the development of tuft cells, a rare chemosensory cells that coordinate immune and neural functions within mucosal epithelial tissues (PubMed:35576971
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17721 DUF5566 3 236 Family of unknown function (DUF5566) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in tuft cells of colon mucosa, as well as in small intestine and thymus (PubMed:35576971). {ECO:0000269|PubMed:25048349, ECO:0000269|PubMed:35576971}.
Sequence
Sequence length 236
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Colorectal Cancer Colorectal cancer, ICD10 C18, C19, C20: colorectal cancer N/A N/A GWAS