Gene Gene information from NCBI Gene database.
Entrez ID 56935
Gene name Single-pass membrane protein with coiled-coil domains 4
Gene symbol SMCO4
Synonyms (NCBI Gene)
C11orf75FN5
Chromosome 11
Chromosome location 11q21
miRNA miRNA information provided by mirtarbase database.
166
miRTarBase ID miRNA Experiments Reference
MIRT004895 hsa-miR-124-3p Microarray 15685193
MIRT016301 hsa-miR-193b-3p Microarray 20304954
MIRT004895 hsa-miR-124-3p Microarray 18668037
MIRT004895 hsa-miR-124-3p Microarray 15685193
MIRT606900 hsa-miR-8485 HITS-CLIP 23824327
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 21516116, 25416956, 32296183
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
609477 24810 ENSG00000166002
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NRQ5
Protein name Single-pass membrane and coiled-coil domain-containing protein 4 (Protein FN5)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15012 DUF4519 1 56 Domain of unknown function (DUF4519) Family
Sequence
Sequence length 59
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
METABOLIC SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations