Gene Gene information from NCBI Gene database.
Entrez ID 148753
Gene name Family with sequence similarity 163 member A
Gene symbol FAM163A
Synonyms (NCBI Gene)
C1orf76NDSP
Chromosome 1
Chromosome location 1q25.2
miRNA miRNA information provided by mirtarbase database.
57
miRTarBase ID miRNA Experiments Reference
MIRT718035 hsa-miR-4685-5p HITS-CLIP 19536157
MIRT718034 hsa-miR-6837-5p HITS-CLIP 19536157
MIRT718033 hsa-miR-1915-3p HITS-CLIP 19536157
MIRT718032 hsa-miR-6764-5p HITS-CLIP 19536157
MIRT718031 hsa-miR-103a-2-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183, 32814053
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611727 28274 ENSG00000143340
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96GL9
Protein name Protein FAM163A (Cebelin) (Neuroblastoma-derived secretory protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15069 FAM163 1 167 FAM163 family Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in neuroblastoma compared to other tissues, suggesting that it may be used as a marker for metastasis in bone marrow. {ECO:0000269|PubMed:17208556}.
Sequence
Sequence length 167
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
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
ASTROCYTOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CENTRAL NERVOUS SYSTEM CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ENDOMETRIOSIS Disgenet
★★☆☆☆
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
Borderline Personality Disorder Borderline personality disorder Pubtator 25612291 Associate
★☆☆☆☆
Found in Text Mining only
Depressive Disorder Major Major depressive disorder Pubtator 25612291 Associate
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 19671756
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 31496741
★☆☆☆☆
Found in Text Mining only
Neuroblastoma Neuroblastoma BEFREE 19671756, 31496741
★☆☆☆☆
Found in Text Mining only
Neuroblastoma Neuroblastoma Pubtator 19671756 Stimulate
★☆☆☆☆
Found in Text Mining only
Squamous cell carcinoma of lung Lung carcinoma BEFREE 31496741
★☆☆☆☆
Found in Text Mining only