SMIM15 (small integral membrane protein 15)

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID 643155
Gene name Small integral membrane protein 15
Gene symbol SMIM15
Synonyms (NCBI Gene)
C5orf43
Chromosome 5
Chromosome location 5q12.1
miRNA miRNA information provided by mirtarbase database.
2022
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (2022)
miRTarBase ID miRNA Experiments Reference
MIRT050930 hsa-miR-17-5p CLASH 23622248
MIRT609108 hsa-miR-548a-5p HITS-CLIP 22927820
MIRT609107 hsa-miR-548ab HITS-CLIP 22927820
MIRT609106 hsa-miR-548ad-5p HITS-CLIP 22927820
MIRT609105 hsa-miR-548ae-5p HITS-CLIP 22927820
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (1)
GO ID Ontology Definition Evidence Reference
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q7Z3B0
Protein name Small integral membrane protein 15
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15086 UPF0542 4 → 71 Uncharacterised protein family UPF0542 Family
Sequence
Sequence length 74
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Gene miRNA Gene ontology Other IDs Protein Associated diseases
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)
Show/Hide Unknown Diseases (1)
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
COLOR VISION DISORDER — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations