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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Delta(24)-sterol reductase
Summary
- UniProt ID
- Q15392
- Gene Symbol
-
- DHCR24
- KIAA0018
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q15392
- PubChem
- Q15392
- SwissLipids
- The Human Metabolome Database
- HMDBP01935
- The O-GlcNAc Database
- Q15392
- RaftProt
- Q15392
Annotation
- Keyword
-
- Alternative splicing
- Cholesterol biosynthesis
- Disease variant
- Endoplasmic reticulum
- FAD
- Golgi apparatus
- NADP
- Oxidoreductase
- Reference proteome
- Signal
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| nucleus |
| cytoplasm |
| membrane |
| endoplasmic reticulum |
| endoplasmic reticulum membrane |
| Golgi membrane |
Sequence
MEPAVSLAVCALLFLLWVRLKGLEFVLIHQRWVFVCLFLLPLSLIFDIYYYVRAWVVFKLSSAPRLHEQRVRDIQKQVREWKEQGSKTFMCTGRPGWLTVSLRVGKYKKTHKNIMINLMDILEVDTKKQIVRVEPLVTMGQVTALLTSIGWTLPVLPELDDLTVGGLIMGTGIESSSHKYGLFQHICTAYELVLADGSFVRCTPSENSDLFYAVPWSCGTLGFLVAAEIRIIPAKKYVKLRFEPVRGLEAICAKFTHESQRQENHFVEGLLYSLDEAVIMTGVMTDEAEPSKLNSIGNYYKPWFFKHVENYLKTNREGLEYIPLRHYYHRHTRSIFWELQDIIPFGNNPIFRYLFGWMVPPKISLLKLTQGETLRKLYEQHHVVQDMLVPMKCLQQALHTFQNDIHVYPIWLCPFILPSQPGLVHPKGNEAELYIDIGAYGEPRVKHFEARSCMRQLEKFVRSVHGFQMLYADCYMNREEFWEMFDGSLYHKLREKLGCQDAFPEVYDKICKAARH
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
|
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Bloch pathway | Homo sapiens |
| Cholesterol biosynthesis | Homo sapiens |
| Kandutsch-Russell pathway | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0040085 | bacterial sepsis | |
| DOID:0050424 | familial adenomatous polyposis | |
| DOID:0050453 | lissencephaly | |
| DOID:0050777 | Joubert syndrome | |
| DOID:0060041 | autism spectrum disorder | |
| DOID:0060270 | pontocerebellar hypoplasia type 2D | |
| DOID:0060276 | pontocerebellar hypoplasia type 7 | |
| DOID:0060277 | pontocerebellar hypoplasia type 8 | |
| DOID:0060278 | pontocerebellar hypoplasia type 9 | |
| DOID:0060292 | X-linked chondrodysplasia punctata 1 |
