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Repository for lectin-assisted multimodality data
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otogelin
Summary
- Gene Symbol
-
- OTOG
- Aliases
-
- FLJ46346
- OTGN
- mlemp
- Organism
- Homo sapiens (human)
Annotation
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| nervous system development | ||
| L-arabinose metabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular space | ||
| apical plasma membrane | ||
| extracellular matrix |
| GO Term | Evidence Code | PMID |
|---|---|---|
| alpha-L-arabinofuranosidase activity |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- otogelin
- Functional Category
-
- E: Amino acid transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
- Q: Secondary metabolites biosynthesis, transport and catabolism
| Gene Ontology |
|---|
| L-arabinose metabolic process |
| alpha-L-arabinofuranosidase activity |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110474 | autosomal recessive nonsyndromic deafness 18B |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000750 | Delayed speech and language development |
| HP:0001756 | Vestibular hypofunction |
| HP:0003577 | Congenital onset |
| Disease ID | Disease Name |
|---|---|
| OMIM:614945 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
