Entity Details

Primary name TECTA
Entity type gene
Source Source Link

Details

PrimaryID7007
RefseqGeneNG_011633
SymbolTECTA
Nametectorin alpha
Chromosome11
Location11q23.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-08-11
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTECTA_HUMAN

GO terms

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GOName
GO:0005201 extracellular matrix structural constituent
GO:0005576 extracellular region
GO:0005886 plasma membrane
GO:0007160 cell-matrix adhesion
GO:0007605 sensory perception of sound
GO:0031225 anchored component of membrane
GO:0062023 collagen-containing extracellular matrix
GO:0070062 extracellular exosome

Diseases

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Disease IDSourceNameDescription
601543 OMIMDeafness, autosomal dominant, 12 (DFNA12)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.
603629 OMIMDeafness, autosomal recessive, 21 (DFNB21)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.

Interactions

3 interactions

InteractorPartnerSourcesPublicationsLink
TECTANEK4BioGRID, MINT25798074 details
TECTADCAF4BioGRID30945288 details
TECTAHNRNPLBioGRID28611215 details