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:0014667 | disease of metabolism | |
DOID:0050387 | nonpapillary renal cell carcinoma | |
DOID:0050424 | familial adenomatous polyposis | |
DOID:0050427 | xeroderma pigmentosum | |
DOID:0050448 | white sponge nevus | |
DOID:0050590 | severe congenital neutropenia | |
DOID:0050639 | primary cutaneous amyloidosis | |
DOID:0050865 | tongue squamous cell carcinoma | |
DOID:0050902 | medulloblastoma | |
DOID:0050908 | myelodysplastic syndrome |
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 |
---|---|---|---|
123799824 | URSAM29251 | ||
100466967 | AILME17244 | ||
101676151 | MUSPF07886 | ||
101099873 | FELCA08013 | ||
122216410 | PANLE02648 | ||
101319238 | TURTR14145 | ||
118906405 | BALMU05300 | ||
100655003 | LOXAF08443 | ||
100070088 | HORSE09336 | ||
100625479 | PIGXX22235 |
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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