GO Term | Evidence Code | PMID |
---|---|---|
cellular response to toxic substance | ||
positive regulation of translation | ||
retinal metabolic process | ||
epoxygenase P450 pathway |
|
|
cellular response to hydrogen peroxide |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
endoplasmic reticulum membrane |
|
|
mitochondrion |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110848 | xeroderma pigmentosum group F | |
DOID:0110849 | xeroderma pigmentosum group G | |
DOID:0110850 | xeroderma pigmentosum group B | |
DOID:0111228 | Sveinsson chorioretinal atrophy | |
DOID:0111441 | optic atrophy 1 | |
DOID:0111529 | familial multiple nevi flammei | |
DOID:10041 | dysplastic nevus syndrome | |
DOID:11716 | prediabetes syndrome | |
DOID:11771 | spontaneous ocular nystagmus | |
DOID:10283 | prostate cancer |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000486 | Strabismus |
HP:0000501 | Glaucoma |
HP:0000505 | Visual impairment |
HP:0000523 | Subcapsular cataract |
HP:0000525 | Abnormality iris morphology |
HP:0000541 | Retinal detachment |
HP:0000557 | Buphthalmos |
HP:0000572 | Visual loss |
HP:0000587 | Abnormal optic nerve morphology |
Disease ID | Disease Name |
---|---|
OMIM:617315 |
|
ORPHA:98976 |
|
OMIM:600975 |
|
ORPHA:98977 |
|
ORPHA:708 |
|
OMIM:231300 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
107586077 | SINGR28061 | ||
106825888 | EQUAS08935 | ||
105292959 | PTEVA08344 | ||
115055310 | ECHNA09814 | ||
115399571 | SALFA52884 | ||
105507461 | COLAP05091 | ||
105818018 | PROCO05798 | ||
109100547 | CYPCA64164 | ||
109100558 | CYPCA80681 | ||
103725278 | NANGA19347 |
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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