GO Term | Evidence Code | PMID |
---|---|---|
benzene-containing compound metabolic process | ||
collagen fibril organization | ||
omega-hydroxylase P450 pathway |
|
|
response to nutrient | ||
DNA modification |
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:0060041 | autism spectrum disorder | |
DOID:0060058 | lymphoma | |
DOID:0060060 | non-Hodgkin lymphoma | |
DOID:0060262 | gallbladder disease | |
DOID:0060287 | cornea plana | |
DOID:0060291 | oculodentodigital dysplasia | |
DOID:0060605 | obsolete anterior segment mesenchymal dysgenesis | |
DOID:0060648 | anterior segment dysgenesis | |
DOID:0060673 | Peters anomaly | |
DOID:0060891 | Parkinson's disease 19A |
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 |
---|---|---|---|
101612471 | JACJA11699 | ||
102417339 | MYOLU01592 | ||
117033397 | RHIFE24644 | ||
100230258 | TAEGU21715 | ||
103220462 | CHLSB04383 | ||
108520884 | RHIBE24276 | ||
104680972 | RHIRO39178 | ||
100583040 | NOMLE15392 | ||
114594484 | PODMU16720 | ||
107549156 | SINGR69202 |
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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