Gene Gene information from NCBI Gene database.
Entrez ID 220323
Gene name Out at first homolog
Gene symbol OAF
Synonyms (NCBI Gene)
NS5ATP13TP2
Chromosome 11
Chromosome location 11q23.3
miRNA miRNA information provided by mirtarbase database.
79
miRTarBase ID miRNA Experiments Reference
MIRT004880 hsa-miR-124-3p Microarray 15685193
MIRT004880 hsa-miR-124-3p Microarray 15685193
MIRT004880 hsa-miR-124-3p Microarray 18668037
MIRT723402 hsa-miR-6736-3p HITS-CLIP 19536157
MIRT723401 hsa-miR-6793-3p HITS-CLIP 19536157
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
621070 28752 ENSG00000184232
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86UD1
Protein name Out at first protein homolog (HCV NS5A-transactivated protein 13 target protein 2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14941 OAF 30 268 Transcriptional regulator, Out at first Family
Sequence
Sequence length 273
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Clear cell carcinoma of kidney Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Ectopia Lentis Ectopia Lentis BEFREE 29305299
★☆☆☆☆
Found in Text Mining only
Irido-corneo-trabecular dysgenesis (disorder) Anterior segment dysgenesis BEFREE 29305299
★☆☆☆☆
Found in Text Mining only