Entity Details

Primary name TMEM260
Entity type gene
Source Source Link

Details

PrimaryID54916
RefseqGene
SymbolTMEM260
Nametransmembrane protein 260
Chromosome14
Location14q22.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-07-03
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTM260_HUMAN

GO terms

Show/Hide Table
GOName
GO:0016021 integral component of membrane

Diseases

Show/Hide Table
Disease IDSourceNameDescription
617478 OMIMStructural heart defects and renal anomalies syndrome (SHDRA)An autosomal recessive syndrome characterized by central nervous system, cardiac, renal, and digit abnormalities. Clinical features include ventricular and atrial septal defects, truncus arteriosus, tetralogy of Fallot, partial anomalous pulmonary venous return, renal cysts, renal failure, and generalized edema. Some patients show partial agenesis of corpus callosum. The disease is caused by variants affecting the gene represented in this entry.

Interactions

8 interactions