Gene Gene information from NCBI Gene database.
Entrez ID 167555
Gene name Family with sequence similarity 151 member B
Gene symbol FAM151B
Synonyms (NCBI Gene)
UNQ9217
Chromosome 5
Chromosome location 5q14.1
miRNA miRNA information provided by mirtarbase database.
169
miRTarBase ID miRNA Experiments Reference
MIRT688332 hsa-miR-6776-5p HITS-CLIP 23313552
MIRT688331 hsa-miR-4252 HITS-CLIP 23313552
MIRT688330 hsa-miR-1262 HITS-CLIP 23313552
MIRT688329 hsa-miR-4701-3p HITS-CLIP 23313552
MIRT688328 hsa-miR-6736-5p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956
GO:0005615 Component Extracellular space IBA
GO:0042461 Process Photoreceptor cell development IEA
GO:0042461 Process Photoreceptor cell development ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6UXP7
Protein name Protein FAM151B
Protein function Essential for survival of retinal photoreceptor cells.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10223 DUF2181 29 263 Uncharacterized conserved protein (DUF2181) Family
Sequence
Sequence length 276
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations