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:0000593 | Abnormal anterior chamber morphology |
HP:0000603 | Central scotoma |
HP:0000639 | Nystagmus |
HP:0000659 | Peters anomaly |
HP:0001052 | Nevus flammeus |
HP:0001087 | Developmental glaucoma |
HP:0001138 | Optic neuropathy |
HP:0003593 | Infantile onset |
HP:0007759 | Opacification of the corneal stroma |
HP:0007854 | Glaucomatous visual field defect |
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 |
---|---|---|---|
105597190 | CERAT39002 | ||
102146810 | MACFA07628 | ||
710385 | MACMU08781 | ||
105464862 | MACNE00758 | ||
101014578 | PAPAN09598 | ||
105551910 | MANLE31230 | ||
101134278 | GORGO24755 | ||
459163 | PANTR27430 | ||
483038 | CANLF05051 | ||
112935290 | VULVU31546 |
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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