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:3748 | esophagus squamous cell carcinoma | |
DOID:3772 | intraventricular meningioma | |
DOID:381 | arthropathy | |
DOID:3829 | pituitary adenoma | |
DOID:3852 | Peutz-Jeghers syndrome | |
DOID:3861 | medullomyoblastoma | |
DOID:3864 | adult medulloblastoma | |
DOID:3868 | melanotic medulloblastoma | |
DOID:3869 | childhood medulloblastoma | |
DOID:3883 | Lynch 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 |
---|---|---|---|
511470 | BOVIN02261 | ||
102184252 | CAPHI01621 | ||
101119706 | SHEEP13930 | ||
100358590 | RABIT08711 | ||
105986861 | DIPOR07022 | ||
13078 | MGI:88590 | MOUSE22049 | |
25426 | RGD:2460 | RATNO34963 | |
100719054 | CAVPO09787 | ||
101580968 | OCTDE05259 | ||
100011610 | MONDO08028 |
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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