Gene Gene information from NCBI Gene database.
Entrez ID 201931
Gene name Transmembrane protein 192
Gene symbol TMEM192
Synonyms (NCBI Gene)
-
Chromosome 4
Chromosome location 4q32.3
miRNA miRNA information provided by mirtarbase database.
790
miRTarBase ID miRNA Experiments Reference
MIRT027253 hsa-miR-101-3p Sequencing 20371350
MIRT028454 hsa-miR-30a-5p Proteomics 18668040
MIRT047317 hsa-miR-181a-5p CLASH 23622248
MIRT685137 hsa-miR-4694-3p HITS-CLIP 23313552
MIRT685136 hsa-miR-4496 HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0005634 Component Nucleus IDA 22736246
GO:0005654 Component Nucleoplasm IDA
GO:0005764 Component Lysosome IDA 22736246
GO:0005764 Component Lysosome IEA
GO:0005765 Component Lysosomal membrane IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620677 26775 ENSG00000170088
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IY95
Protein name Transmembrane protein 192
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14802 TMEM192 26 259 TMEM192 family Family
Tissue specificity TISSUE SPECIFICITY: Strongly expressed in kidney, liver, lung and pancreas. {ECO:0000269|PubMed:20370317}.
Sequence
Sequence length 271
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
NEUROTIC DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
POLYCYSTIC OVARY SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Mouth Neoplasms Associate 36626444
★☆☆☆☆
Found in Text Mining only