Gene Gene information from NCBI Gene database.
Entrez ID 56889
Gene name Transmembrane 9 superfamily member 3
Gene symbol TM9SF3
Synonyms (NCBI Gene)
EP70-P-isoSMBP
Chromosome 10
Chromosome location 10q24.1
miRNA miRNA information provided by mirtarbase database.
1076
miRTarBase ID miRNA Experiments Reference
MIRT000166 hsa-miR-21-5p Luciferase reporter assay 19253296
MIRT016580 hsa-miR-193b-3p Proteomics 21512034
MIRT019233 hsa-miR-331-3p Sequencing 20371350
MIRT023025 hsa-miR-124-3p Microarray 18668037
MIRT025193 hsa-miR-181a-5p Sequencing 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0016020 Component Membrane IBA
GO:0016020 Component Membrane IEA
GO:0072657 Process Protein localization to membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616872 21529 ENSG00000077147
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9HD45
Protein name Transmembrane 9 superfamily member 3 (EP70-P-iso) (SM-11044-binding protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02990 EMP70 57 546 Endomembrane protein 70 Family
Sequence
Sequence length 589
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
SCOLIOSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Adult T-Cell Lymphoma/Leukemia T-Cell Lymphoma/Leukemia BEFREE 28390114
★☆☆☆☆
Found in Text Mining only
Leukemia, T-Cell T-cell leukemia BEFREE 28390114
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of stomach Stomach Neoplasms BEFREE 24642718, 26033320
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 24642718
★☆☆☆☆
Found in Text Mining only
Stomach Carcinoma Stomach Carcinoma BEFREE 24642718, 26033320
★☆☆☆☆
Found in Text Mining only