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 1 - 10 of 143 in total
DO ID Disease Name Source
DOID:0050564 autosomal dominant nonsyndromic deafness
DOID:0050565 autosomal recessive nonsyndromic deafness
DOID:0050566 X-linked nonsyndromic deafness
DOID:0050811 congenital adrenal hyperplasia
DOID:0060295 complement component 2 deficiency
DOID:0060574 von Willebrand's disease 2
DOID:0060690 autosomal dominant auditory neuropathy 1
DOID:0110462 autosomal recessive nonsyndromic deafness 101
DOID:0110463 autosomal recessive nonsyndromic deafness 102
DOID:0110464 autosomal recessive nonsyndromic deafness 103
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

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024