Gene Gene information from NCBI Gene database.
Entrez ID 202915
Gene name Transmembrane protein 184A
Gene symbol TMEM184A
Synonyms (NCBI Gene)
SDMG1SLC51C1
Chromosome 7
Chromosome location 7p22.3
miRNA miRNA information provided by mirtarbase database.
444
miRTarBase ID miRNA Experiments Reference
MIRT723959 hsa-miR-6752-3p HITS-CLIP 19536157
MIRT723958 hsa-miR-1913 HITS-CLIP 19536157
MIRT723957 hsa-miR-324-3p HITS-CLIP 19536157
MIRT723956 hsa-miR-3190-5p HITS-CLIP 19536157
MIRT723955 hsa-miR-3176 HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0005737 Component Cytoplasm IEA
GO:0005768 Component Endosome IEA
GO:0005768 Component Endosome ISS
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane ISS
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.
Q6ZMB5
Protein name Transmembrane protein 184A
Protein function Acts as a heparin receptor in vascular cells (By similarity). May be involved in vesicle transport in exocrine cells and Sertoli cells (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03619 Solute_trans_a 55 329 Organic solute transporter Ostalpha Family
Tissue specificity TISSUE SPECIFICITY: Expressed in vascular cells (at protein level). {ECO:0000269|PubMed:26769966}.
Sequence
Sequence length 413
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PEPTIC ULCER DISEASE 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
Ovarian Diseases Ovarian diseases Pubtator 37033258 Associate
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Stomach neoplasms Pubtator 34925643 Associate
★☆☆☆☆
Found in Text Mining only