Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5450
Gene name Gene Name - the full gene name approved by the HGNC.
POU class 2 homeobox associating factor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
POU2AF1
Synonyms (NCBI Gene) Gene synonyms aliases
BOB1, OBF-1, OBF1, OCAB
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
MIRT439929 ebv-miR-BART4-5p HITS-CLIP 22473208
MIRT439928 hsa-miR-210-3p HITS-CLIP 22473208
MIRT439929 ebv-miR-BART4-5p HITS-CLIP 22473208
MIRT726902 hsa-miR-15a-5p HITS-CLIP 22473208
MIRT726901 hsa-miR-15b-5p HITS-CLIP 22473208
Transcription factors
Transcription factor Regulation Reference
POU2F1 Unknown 11847120
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002314 Process Germinal center B cell differentiation IEA
GO:0002314 Process Germinal center B cell differentiation ISS
GO:0003677 Function DNA binding IEA
GO:0003712 Function Transcription coregulator activity TAS 7859290
GO:0003713 Function Transcription coactivator activity IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601206 9211 ENSG00000110777
Protein
UniProt ID Q16633
Protein name POU domain class 2-associating factor 1 (B-cell-specific coactivator OBF-1) (BOB-1) (OCA-B) (OCT-binding factor 1)
Protein function Transcriptional coactivator that specifically associates with either POU2F1/OCT1 or POU2F2/OCT2 (PubMed:7859290). It boosts the POU2F1/OCT1 mediated promoter activity and to a lesser extent, that of POU2F2/OCT2 (PubMed:7779176). It recognizes th
PDB 1CQT
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09310 PD-C2-AF1 7 255 POU domain, class 2, associating factor 1 Domain
Tissue specificity TISSUE SPECIFICITY: B-cell specific (PubMed:7779176, PubMed:7859290). Detected in mainly in spleen, but also in thymus, periphral blood leukocyte and small intestine (PubMed:7779176, PubMed:7859290). {ECO:0000269|PubMed:7779176, ECO:0000269|PubMed:7859290
Sequence
Sequence length 256
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
Agammaglobulinemia agammaglobulinemia N/A N/A GenCC
Biliary Cholangitis Primary biliary cholangitis N/A N/A GWAS
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Multiple Sclerosis Multiple sclerosis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Acute Radiation Syndrome Associate 33476246, 35680903, 37676284, 38499035
Adenocarcinoma of Lung Associate 38015097
Aortic Aneurysm Abdominal Associate 34637689
Arthritis Rheumatoid Associate 33004899
Carcinoma Renal Cell Associate 32012488
Common Variable Immunodeficiency Associate 21905497
COVID 19 Associate 37040675
Epstein Barr Virus Infections Associate 20016960
Gastrointestinal Stromal Tumors Inhibit 29578181
Hematologic Diseases Associate 37676284