tectorin alpha

Summary
Gene Symbol
  • TECTA
Organism
Homo sapiens (human)
External Links
NCBI Gene
7007
HGNC
11720
KEGG Gene ID
hsa:7007
PubChem
7007
Alliance of Genome Resources
Annotation
Keyword
  • Cell membrane
  • Disease variant
  • Disulfide bond
  • Extracellular matrix
  • GPI-anchor
  • Hearing
  • Non-syndromic deafness
  • Reference proteome
  • Repeat
  • Signal
Proteins
Displaying 1 entry
UniProt Protein Name
O75443
Gene Ontology (GO)
KEGG BRITE Database
Orthology
K18273
Name
alpha-tectorin
References
Disease
Disease Ontology
Displaying entries 21 - 30 of 142 in total
DO ID Disease Name Source
DOID:0110477 autosomal recessive nonsyndromic deafness 2
DOID:0110478 autosomal recessive nonsyndromic deafness 20
DOID:0110479 autosomal recessive nonsyndromic deafness 21
DOID:0110480 autosomal recessive nonsyndromic deafness 22
DOID:0110481 autosomal recessive nonsyndromic deafness 23
DOID:0110482 autosomal recessive nonsyndromic deafness 24
DOID:0110483 autosomal recessive nonsyndromic deafness 25
DOID:0110484 autosomal recessive nonsyndromic deafness 26
DOID:0110485 autosomal recessive nonsyndromic deafness 27
DOID:0110486 autosomal recessive nonsyndromic deafness 28
The Human Phenotype Ontology
Displaying all 3 entries
HPO ID HPO Term
HP:0000006 Autosomal dominant inheritance
HP:0000007 Autosomal recessive inheritance
HP:0000407 Sensorineural hearing impairment
Displaying all 2 entries
Disease ID Disease Name
OMIM:603629
  • autosomal recessive nonsyndromic hearing loss 21
OMIM:601543
  • autosomal dominant nonsyndromic hearing loss 12

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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