UniProt | Protein Name |
---|---|
O00468 |
|
GO Term | Evidence Code | PMID |
---|---|---|
clustering of voltage-gated sodium channels |
|
GO Term | Evidence Code | PMID |
---|---|---|
extracellular region |
|
|
Golgi lumen |
|
|
basement membrane | ||
synapse | ||
plasma membrane |
|
GO Term | Evidence Code | PMID |
---|---|---|
dystroglycan binding | ||
laminin binding |
|
|
chondroitin sulfate binding | ||
calcium ion binding | ||
heparan sulfate proteoglycan binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:10003 | sensorineural hearing loss | |
DOID:10293 | monocular esotropia | |
DOID:1059 | intellectual disability | |
DOID:10652 | Alzheimer's disease | |
DOID:11771 | spontaneous ocular nystagmus | |
DOID:11832 | visual epilepsy | |
DOID:11870 | Pick's disease | |
DOID:11963 | esophagitis | |
DOID:12506 | Bell's palsy | |
DOID:13174 | dissociated nystagmus |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000218 | High palate |
HP:0000276 | Long face |
HP:0000308 | Microretrognathia |
HP:0000369 | Low-set ears |
HP:0000407 | Sensorineural hearing impairment |
HP:0000467 | Neck muscle weakness |
HP:0000496 | Abnormality of eye movement |
HP:0000508 | Ptosis |
HP:0000565 | Esotropia |
Disease ID | Disease Name |
---|---|
ORPHA:98913 |
|
ORPHA:98914 |
|
OMIM:615120 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
525795 | BOVIN08530 | ||
102169403 | CAPHI07001 | ||
101107299 | SHEEP03852 | ||
100765949 | CRIGR19976 | ||
11603 | MGI:87961 | MOUSE41401 | |
25592 | RGD:2067 | RATNO33347 | |
100716304 | CAVPO24564 | ||
113906726 | BOBOX05594 | ||
101076403 | TAKRU37574 | ||
105727803 | AOTNA38005 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024