Gene Gene information from NCBI Gene database.
Entrez ID 55751
Gene name Transmembrane protein 184C
Gene symbol TMEM184C
Synonyms (NCBI Gene)
SLC51C3TMEM34
Chromosome 4
Chromosome location 4q31.23
miRNA miRNA information provided by mirtarbase database.
502
miRTarBase ID miRNA Experiments Reference
MIRT047195 hsa-miR-182-5p CLASH 23622248
MIRT719010 hsa-miR-153-5p HITS-CLIP 19536157
MIRT719009 hsa-miR-627-3p HITS-CLIP 19536157
MIRT719008 hsa-miR-4641 HITS-CLIP 19536157
MIRT719007 hsa-miR-431-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0016020 Component Membrane IBA
GO:0016020 Component Membrane IEA
GO:0022857 Function Transmembrane transporter activity IBA
GO:0055085 Process Transmembrane transport IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
613937 25587 ENSG00000164168
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NVA4
Protein name Transmembrane protein 184C (Transmembrane protein 34)
Protein function Possible tumor suppressor which may play a role in cell growth.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03619 Solute_trans_a 48 317 Organic solute transporter Ostalpha Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed with higher expression in lung, kidney, spleen, pancreas, thymus, prostate, testis, ovary, small intestine and thyroid. {ECO:0000269|PubMed:17072649}.
Sequence
Sequence length 438
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
COLORECTAL CANCER 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
Anaplastic thyroid carcinoma Anaplastic thyroid cancer BEFREE 17072649
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of thyroid Thyroid cancer BEFREE 17072649
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 17072649
★☆☆☆☆
Found in Text Mining only
Thyroid carcinoma Thyroid Carcinoma BEFREE 17072649
★☆☆☆☆
Found in Text Mining only
Thyroid Neoplasm Thyroid Neoplasm LHGDN 17072649
★☆☆☆☆
Found in Text Mining only