Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
81615
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 163
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM163
Synonyms (NCBI Gene) Gene synonyms aliases
DC29, HLD25, SLC30A11, SV31
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q21.3
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618978 25380 ENSG00000152128
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Biliary Cholangitis Primary biliary cholangitis N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Leukodystrophy leukodystrophy, hypomyelinating, 25 N/A N/A GenCC
Associations from Text Mining Disease 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