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 131 - 140 of 142 in total
DO ID Disease Name Source
DOID:0110587 autosomal dominant nonsyndromic deafness 66
DOID:0110588 autosomal dominant nonsyndromic deafness 67
DOID:0110589 autosomal dominant nonsyndromic deafness 68
DOID:0110590 autosomal dominant nonsyndromic deafness 69
DOID:0110591 autosomal dominant nonsyndromic deafness 7
DOID:0110592 autosomal dominant nonsyndromic deafness 70
DOID:0110593 autosomal dominant nonsyndromic deafness 9
DOID:0111414 trichohepatoenteric syndrome
DOID:0111415 trichohepatoenteric syndrome 1
DOID:10003 sensorineural hearing loss
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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