UniProt | Protein Name |
---|---|
O15528 |
|
GO Term | Evidence Code | PMID |
---|---|---|
calcium ion transport | ||
negative regulation of calcidiol 1-monooxygenase activity | ||
G1 to G0 transition | ||
response to estrogen | ||
response to lipopolysaccharide |
GO Term | Evidence Code | PMID |
---|---|---|
cytoplasm | ||
mitochondrial outer membrane |
|
|
mitochondrion |
GO Term | Evidence Code | PMID |
---|---|---|
iron ion binding | ||
secalciferol 1-monooxygenase activity | ||
calcidiol 1-monooxygenase activity | ||
heme binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:2349 | arteriosclerosis | |
DOID:235 | colonic benign neoplasm | |
DOID:2351 | iron metabolism disease | |
DOID:2352 | hemochromatosis | |
DOID:2377 | multiple sclerosis | |
DOID:2394 | ovarian cancer | |
DOID:240 | iris disease | |
DOID:2468 | psychotic disorder | |
DOID:2485 | phosphorus metabolism disease | |
DOID:2513 | basal cell carcinoma |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000684 | Delayed eruption of teeth |
HP:0000737 | Irritability |
HP:0000867 | Secondary hyperparathyroidism |
HP:0000886 | Deformed rib cage |
HP:0000893 | Bulging of the costochondral junction |
HP:0000897 | Rachitic rosary |
HP:0000920 | Enlargement of the costochondral junction |
HP:0001252 | Hypotonia |
HP:0001270 | Motor delay |
Disease ID | Disease Name |
---|---|
OMIM:264700 |
|
ORPHA:289157 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
173936 | WB:WBGene00000375 | ||
36105 | FB:FBgn0033524 | ||
36378 | FB:FBgn0033753 | ||
37163 | FB:FBgn0034387 | ||
40037 | FB:FBgn0036806 | ||
41272 | FB:FBgn0037817 | ||
42293 | FB:FBgn0038680 | ||
42294 | FB:FBgn0038681 | ||
246648 | FB:FBgn0050489 | ||
2768720 | FB:FBgn0053503 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024