autosomal recessive nonsyndromic deafness 68

Summary
Synonym
  • DFNB68
  • autosomal recessive deafness 68
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the S1PR2 gene on chromosome 19p13.
Super Class
autosomal recessive nonsyndromic deafness
Disease Ontology
DOID:0110519
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9294 S1PR2 sphingosine-1-phosphate receptor 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
14739 S1pr2 sphingosine-1-phosphate receptor 2
Related Glycoprotein

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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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Last updated: April 7, 2025