Gene Gene information from NCBI Gene database.
Entrez ID 400451
Gene name Family with sequence similarity 174 member B
Gene symbol FAM174B
Synonyms (NCBI Gene)
-
Chromosome 15
Chromosome location 15q26.1
miRNA miRNA information provided by mirtarbase database.
356
miRTarBase ID miRNA Experiments Reference
MIRT611220 hsa-miR-8485 HITS-CLIP 23824327
MIRT672171 hsa-miR-6767-3p HITS-CLIP 23824327
MIRT611219 hsa-miR-4328 HITS-CLIP 23824327
MIRT635527 hsa-miR-8064 HITS-CLIP 23824327
MIRT630472 hsa-miR-125a-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0005794 Component Golgi apparatus IDA 29851555
GO:0005794 Component Golgi apparatus IEA
GO:0005886 Component Plasma membrane IDA 29851555
GO:0005886 Component Plasma membrane IEA
GO:0007030 Process Golgi organization IMP 29851555
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.
Q3ZCQ3
Protein name Membrane protein FAM174B
Protein function Essential for Golgi structural integrity.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06679 DUF1180 6 159 Protein of unknown function (DUF1180) Family
Sequence
Sequence length 159
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
MIGRAINE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations