UniProt | Protein Name |
---|---|
Q9H8P0 |
|
GO Term | Evidence Code | PMID |
---|---|---|
androgen biosynthetic process |
|
|
dolichol metabolic process | ||
polyprenol catabolic process | ||
dolichol-linked oligosaccharide biosynthetic process | ||
dolichol biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum | ||
endoplasmic reticulum membrane |
|
GO Term | Evidence Code | PMID |
---|---|---|
oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor | ||
polyprenol reductase activity | ||
3-oxo-5-alpha-steroid 4-dehydrogenase activity | ||
3-oxo-5alpha-steroid 4-dehydrogenase (NADP+) |
DO ID | Disease Name | Source |
---|---|---|
DOID:4028 | angioma serpiginosum | |
DOID:4090 | agnosia | |
DOID:420 | hypertrichosis | |
DOID:483 | cavernous hemangioma | |
DOID:5212 | congenital disorder of glycosylation | |
DOID:5614 | eye disease | |
DOID:5723 | optic atrophy | |
DOID:7378 | pituitary hypoplasia | |
DOID:758 | situs inversus | |
DOID:83 | cataract |
HPO ID | HPO Term |
---|---|
HP:0000962 | Hyperkeratosis |
HP:0000964 | Eczematoid dermatitis |
HP:0000973 | Cutis laxa |
HP:0000982 | Palmoplantar keratoderma |
HP:0000998 | Hypertrichosis |
HP:0001000 | Abnormality of skin pigmentation |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001251 | Ataxia |
HP:0001252 | Hypotonia |
Disease ID | Disease Name |
---|---|
OMIM:612379 |
|
ORPHA:324737 |
|
OMIM:612713 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
110200149 | PHACI03073 | ||
101035698 | SAIBB22449 | ||
101958155 | ICTTR02164 | ||
118318277 | SCOMX04547 | ||
102442157 | MYOLU08363 | ||
117022239 | RHIFE18822 | ||
100224163 | TAEGU23558 | ||
103235668 | CHLSB16369 | ||
108531594 | RHIBE04210 | ||
104662017 | RHIRO35627 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024