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Gene : TMCO3 Homo sapiens

Name  ? transmembrane and coiled-coil domains 3 Cytological Location  13q34
Brief Description  transmembrane and coiled-coil domains 3
Description  This gene encodes a member of the monovalent cation:proton antiporter 2 (CPA2) family of transporter proteins. Members of this family typically couple the export of monovalent cations, such as potassium or sodium, to the import of protons across cellular membranes. Mutations in this gene have been identified in patients with a rare inherited vision defect, cornea guttata with anterior polar cataract. [provided by RefSeq, Mar 2017]
  • synonyms:
  • C13orf11,
  • TMCO3,
  • uc001vtu.5,
  • OTTHUMG00000017389,
  • HGNC:20329,
  • BC012564,
  • FLJ20623,
  • chromosome 13 open reading frame 11,
  • C13orf11,
  • NM_017905
  • identifiers:
  • 55002,
  • ENSG00000150403,
  • TMCO3

Genome feature

Region: gene ? Length: 59237  
Location: 13:113490993-113550229 Cyto location: 13q34

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

3756 SN Ps

5 Cross References

17 Data Sets

2 Homologues

0 Located Features

97 Rna Seq Results