UniProt | Protein Name |
---|---|
Q07973 |
|
GO Term | Evidence Code | PMID |
---|---|---|
vitamin D catabolic process | ||
vitamin D metabolic process |
|
|
vitamin D receptor signaling pathway |
|
|
osteoblast differentiation | ||
vitamin metabolic process |
|
GO Term | Evidence Code | PMID |
---|---|---|
mitochondrial inner membrane |
|
GO Term | Evidence Code | PMID |
---|---|---|
vitamin D 25-hydroxylase activity | ||
1-alpha,25-dihydroxyvitamin D3 23-hydroxylase activity | ||
iron ion binding | ||
1-alpha,25-dihydroxyvitamin D3 24-hydroxylase activity | ||
25-hydroxycholecalciferol-23-hydroxylase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0110741 | type 1 diabetes mellitus 2 | |
DOID:0110742 | type 1 diabetes mellitus 3 | |
DOID:4386 | myofibroma | |
DOID:0110743 | type 1 diabetes mellitus 4 | |
DOID:0110744 | type 1 diabetes mellitus 5 | |
DOID:0110745 | type 1 diabetes mellitus 6 | |
DOID:0110746 | type 1 diabetes mellitus 7 | |
DOID:0110747 | type 1 diabetes mellitus 8 | |
DOID:0110748 | obsolete type 1 diabetes mellitus 9 | |
DOID:0110749 | type 1 diabetes mellitus 10 |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000103 | Polyuria |
HP:0000121 | Nephrocalcinosis |
HP:0000787 | Nephrolithiasis |
HP:0001252 | Hypotonia |
HP:0001254 | Lethargy |
HP:0001508 | Failure to thrive |
HP:0001824 | Weight loss |
HP:0001944 | Dehydration |
HP:0002013 | Vomiting |
Disease ID | Disease Name |
---|---|
OMIM:143880 |
|
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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Last updated: August 19, 2024