GO Term | Evidence Code | PMID |
---|---|---|
sensory perception of sound | ||
transmission of nerve impulse | ||
cell-matrix adhesion |
GO Term | Evidence Code | PMID |
---|---|---|
extracellular region |
|
|
cell surface | ||
plasma membrane |
|
|
side of membrane | ||
apical plasma membrane |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050564 | autosomal dominant nonsyndromic deafness | |
DOID:0050565 | autosomal recessive nonsyndromic deafness | |
DOID:0050566 | X-linked nonsyndromic deafness | |
DOID:0050811 | congenital adrenal hyperplasia | |
DOID:0060295 | complement component 2 deficiency | |
DOID:0060574 | von Willebrand's disease 2 | |
DOID:0060690 | autosomal dominant auditory neuropathy 1 | |
DOID:0110462 | autosomal recessive nonsyndromic deafness 101 | |
DOID:0110463 | autosomal recessive nonsyndromic deafness 102 | |
DOID:0110464 | autosomal recessive nonsyndromic deafness 103 |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000407 | Sensorineural hearing impairment |
Disease ID | Disease Name |
---|---|
OMIM:607039 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
102690494 | LEPOC03951 | ||
100007015 | ZFIN:ZDB-GENE-100922-124 | ||
446273 | Xenbase:XB-GENE-5811284 | ||
100490578 | Xenbase:XB-GENE-5811283 | ||
101943041 | CHRPI01300 | ||
100076809 | ORNAN15805 | ||
100403954 | CALJA07559 | ||
105586254 | CERAT31893 | ||
102142073 | MACFA24504 | ||
699600 | MACMU25834 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024