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:3112 | papillary adenocarcinoma | |
DOID:3635 | congenital myasthenic syndrome | |
DOID:3910 | lung adenocarcinoma | |
DOID:3969 | thyroid gland papillary carcinoma | |
DOID:4090 | agnosia | |
DOID:4465 | papillary renal cell carcinoma | |
DOID:4766 | embryoma | |
DOID:539 | ophthalmoplegia | |
DOID:681 | progressive bulbar palsy | |
DOID:8488 | polyhydramnios |
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 |
---|---|---|---|
101612657 | JACJA09189 | ||
117026787 | RHIFE02847 | ||
100219336 | TAEGU12752 | ||
103225827 | CHLSB09519 | ||
108516787 | RHIBE40547 | ||
104673225 | RHIRO40549 | ||
100590158 | NOMLE23125 | ||
114602499 | PODMU32526 | ||
107591095 | SINGR25015 | ||
107593945 | SINGR55766 |
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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