Gene Gene information from NCBI Gene database.
Entrez ID 81615
Gene name Transmembrane protein 163
Gene symbol TMEM163
Synonyms (NCBI Gene)
DC29HLD25SLC30A11SV31
Chromosome 2
Chromosome location 2q21.3
miRNA miRNA information provided by mirtarbase database.
28
miRTarBase ID miRNA Experiments Reference
MIRT017779 hsa-miR-335-5p Microarray 18185580
MIRT641381 hsa-miR-1255b-2-3p HITS-CLIP 23824327
MIRT641381 hsa-miR-1255b-2-3p HITS-CLIP 23824327
MIRT1431799 hsa-miR-125a-3p CLIP-seq
MIRT1431800 hsa-miR-1271 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
21
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25130899, 36204728
GO:0005764 Component Lysosome IEA
GO:0005765 Component Lysosomal membrane IEA
GO:0005768 Component Endosome IEA
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618978 25380 ENSG00000152128
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TC26
Protein name Transmembrane protein 163
Protein function Zinc ion transporter that mediates zinc efflux and plays a crucial role in intracellular zinc homeostasis (PubMed:25130899, PubMed:31697912, PubMed:36204728). Binds the divalent cations Zn(2+), Ni(2+), and to a minor extent Cu(2+) (By similarity
Family and domains
Tissue specificity TISSUE SPECIFICITY: Widely expressed. High expression is detected in brain, lung and testis. {ECO:0000269|PubMed:25130899}.
Sequence
MEPAAGIQRRSSQGPTVPPPPRGHAPPAAAPGPAPLSSPVREPPQLEEERQVRISESGQF
SDGLEDRGLLESSTRLKPHEAQNYRKKALWVSWFSIIVTLALAVAAFTVSVMRYSASAFG
FAFDAILDVLSSAIVLWRYSNAAAVHSAHREYIACVILGVIFLLSSICIVVKAIHDLSTR
LLPEVDDFLFSVSILSGILCSILAVLKFMLGKVLTSRALITDGFNSLVGGVMGFSILLSA
EVFKHDSAVWYLDGSIGVLIGLTIFAYGVKLLIDMVPRVRQTRHYEMFE
Sequence length 289
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
6
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Leukodystrophy, hypomyelinating, 25 Likely pathogenic; Pathogenic rs2467325671, rs2468508886, rs2468508848 RCV003152356
RCV003152357
RCV003152358
RCV003152359
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 35205284
Carcinoma Pancreatic Ductal Associate 33574088
Diabetes Mellitus Type 2 Associate 26290879
Parkinson Disease Associate 27393345, 33523105