Entity Details

Primary name TMIE
Entity type gene
Source Source Link

Details

PrimaryID259236
RefseqGeneNG_011628
SymbolTMIE
Nametransmembrane inner ear
Chromosome3
Location3p21.31
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-08-09
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTMIE_HUMAN

GO terms

Show/Hide Table
GOName
GO:0007605 sensory perception of sound
GO:0016021 integral component of membrane
GO:0042472 inner ear morphogenesis

Diseases

Show/Hide Table
Disease IDSourceNameDescription
600971 OMIMDeafness, autosomal recessive, 6 (DFNB6)A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. The disease is caused by variants affecting the gene represented in this entry.