otoancorin

Summary
Gene Symbol
  • OTOA
Aliases
  • CT108
  • cancer/testis antigen 108
Organism
Homo sapiens (human)
External Links
NCBI Gene
146183
HGNC
16378
KEGG Gene ID
hsa:146183
PubChem
146183
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cell membrane
  • Extracellular matrix
  • GPI-anchor
  • Hearing
  • Membrane
  • Non-syndromic deafness
  • Reference proteome
  • Signal
Proteins
Displaying all 2 entries
UniProt Protein Name
Q7RTW8
Q05BM7
KEGG BRITE Database
Orthology
K25029
Name
otoancorin
References
Disease
Disease Ontology
Displaying entries 41 - 50 of 143 in total
DO ID Disease Name Source
DOID:0110495 autosomal recessive nonsyndromic deafness 37
DOID:0110496 autosomal recessive nonsyndromic deafness 38
DOID:0110497 autosomal recessive nonsyndromic deafness 39
DOID:0110498 autosomal recessive nonsyndromic deafness 4
DOID:0110499 autosomal recessive nonsyndromic deafness 40
DOID:0110500 autosomal recessive nonsyndromic deafness 42
DOID:0110501 autosomal recessive nonsyndromic deafness 44
DOID:0110502 autosomal recessive nonsyndromic deafness 45
DOID:0110503 autosomal recessive nonsyndromic deafness 46
DOID:0110504 autosomal recessive nonsyndromic deafness 47
The Human Phenotype Ontology
Displaying all 2 entries
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000407 Sensorineural hearing impairment
Displaying 1 entry
Disease ID Disease Name
OMIM:607039
  • autosomal recessive nonsyndromic hearing loss 22

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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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