Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / OrganismsTools
SugarDrawer
GlycanBuilder
Glycan Converters
GlycoMaple
GlycomeAtlas
LM-GlycomeAtlas
GALAXY
MCAW
GlycoSim
GRable
Guidelines
MIRAGE
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
- ORDO
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 64072 | CDH23 | cadherin related 23 | |
| 84899 | TMTC4 | transmembrane O-mannosyltransferase targeting cadherins 4 | |
| 93035 | PKHD1L1 | PKHD1 like 1 | |
| 165829 | GPR156 | G protein-coupled receptor 156 | |
| 645104 | CLRN2 | clarin 2 | |
| 100127206 | MINAR2 | membrane integral NOTCH2 associated receptor 2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| A0PK11 | Clarin-2 | |
| P59773 | Major intrinsically disordered NOTCH2-binding receptor 1-like | |
| Q5T4D3 | Protein O-mannosyl-transferase TMTC4 | |
| Q86WI1 | Fibrocystin-L | |
| Q8NFN8 | Probable G-protein coupled receptor 156 | |
| Q9H251 | Cadherin-23 |
