Gene Gene information from NCBI Gene database.
Entrez ID 400823
Gene name Family with sequence similarity 177 member B
Gene symbol FAM177B
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1q41
miRNA miRNA information provided by mirtarbase database.
14
miRTarBase ID miRNA Experiments Reference
MIRT982213 hsa-miR-4251 CLIP-seq
MIRT982214 hsa-miR-4303 CLIP-seq
MIRT982215 hsa-miR-4329 CLIP-seq
MIRT982216 hsa-miR-4778-5p CLIP-seq
MIRT982217 hsa-miR-539 CLIP-seq
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.
A6PVY3
Protein name Protein FAM177B
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14774 FAM177 6 122 FAM177 family Family
Sequence
Sequence length 158
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
MYOCARDIAL INFARCTION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations