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Standards Ontologies Notations
autosomal dominant nonsyndromic deafness 25

Summary
Synonym
  • DFNA25
  • autosomal dominant deafness 25
Definition
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second-sixth decade of life with high frequency progressive hearing loss and has_material_basis_in mutation in the SLC17A8 gene on chromosome 12q23.
Super Class
autosomal dominant nonsyndromic deafness
Disease Ontology
DOID:0110555
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
246213 SLC17A8 solute carrier family 17 member 8
Displaying all 2 entries
Gene ID Gene Symbol Description Source
63873 Trpv4 transient receptor potential cation channel, subfamily V, member 4
216227 Slc17a8 solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8
Displaying 1 entry
Gene ID Gene Symbol Description Source
266767 Slc17a8 solute carrier family 17 member 8
Displaying 1 entry
Gene ID Gene Symbol Description Source
563467 slc17a8 solute carrier family 17 member 8
Displaying all 3 entries
Gene ID Gene Symbol Description Source
176291 eat-4 Major facilitator superfamily (MFS) profile domain-containing protein;putative vesicular glutamate transporter eat-4
176441 vglu-2 Major facilitator superfamily (MFS) profile domain-containing protein
176442 vglu-3 putative vesicular glutamate transporter vglu-3
Displaying 1 entry
Gene ID Gene Symbol Description Source
850671 YCT1 Yct1p
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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

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Last updated: December 9, 2024