SERTM1 (serine rich and transmembrane domain containing 1)

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID 400120
Gene name Serine rich and transmembrane domain containing 1
Gene symbol SERTM1
Synonyms (NCBI Gene)
C13orf36
Chromosome 13
Chromosome location 13q13.3
miRNA miRNA information provided by mirtarbase database.
116
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (116)
miRTarBase ID miRNA Experiments Reference
MIRT509774 hsa-miR-5580-3p HITS-CLIP 21572407
MIRT509772 hsa-miR-6074 HITS-CLIP 21572407
MIRT542174 hsa-miR-6867-5p HITS-CLIP 21572407
MIRT509769 hsa-miR-3924 HITS-CLIP 21572407
MIRT509770 hsa-miR-210-3p HITS-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (3)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0016020 Component Membrane IEA
GO:0043231 Component Intracellular membrane-bounded organelle IBA
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.
A2A2V5
Protein name Serine-rich and transmembrane domain-containing protein 1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15872 SRTM1 1 → 106 Serine-rich and transmembrane domain-containing protein 1 Family
Sequence
Sequence length 107
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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 (5)
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
BRONCHOPNEUMONIA — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CONGENITAL ANOMALY OF CARDIOVASCULAR SYSTEM — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PARKINSON DISEASE — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PERIPHERAL VASCULAR DISEASE — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations