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Standards Ontologies Notations
autosomal recessive nonsyndromic deafness

Summary
Definition
A nonsyndromic deafness characterized by an autosomal recessive inheritance mode.
Super Class
autosomal recessive disease nonsyndromic deafness
External Links
Disease Ontology
DOID:0050565
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 12 of 12 in total
Gene ID Gene Symbol Description Source
220074 LRTOMT leucine rich transmembrane and O-methyltransferase domain containing
340990 OTOG otogelin
Displaying 1 entry
Gene ID Gene Symbol Description Source
70551 Tmtc4 transmembrane and tetratricopeptide repeat containing 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
290501 Tmtc4 transmembrane O-mannosyltransferase targeting cadherins 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
41867 Tmtc4 Transmembrane O-mannosyltransferase targeting cadherins 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
560605 tmtc4 transmembrane O-mannosyltransferase targeting cadherins 4
Displaying all 2 entries
Gene ID Gene Symbol Description Source Organism
100158586 tmtc4 transmembrane and tetratricopeptide repeat containing 4 Xenopus tropicalis (tropical clawed frog)
108708472 tmtc4.L transmembrane and tetratricopeptide repeat containing 4 L homeolog Xenopus laevis (African clawed frog)
Displaying 1 entry
Gene ID Gene Symbol Description Source
185454 F38B6.6 Protein O-mannosyl-transferase F38B6.6
Related Glycoprotein
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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: August 19, 2024