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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Aldehyde dehydrogenase family 3 member A2
Summary
- UniProt ID
- P51648
- Gene Symbol
-
- ALDH3A2
- ALDH10
- FALDH
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P51648
- PubChem
- P51648
- SwissLipids
- The Human Metabolome Database
- HMDBP00296
- The O-GlcNAc Database
- P51648
- RaftProt
- P51648
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Direct protein sequencing
- Disease variant
- Fatty acid metabolism
- Ichthyosis
- Intellectual disability
- Microsome
- NAD
- Oxidoreductase
- Phosphoprotein
- Reference proteome
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| peroxisome |
| cytosol |
| endoplasmic reticulum membrane |
| peroxisomal membrane |
| cytoplasm |
| intracellular membrane-bounded organelle |
Sequence
MELEVRRVRQAFLSGRSRPLRFRLQQLEALRRMVQEREKDILTAIAADLCKSEFNVYSQEVITVLGEIDFMLENLPEWVTAKPVKKNVLTMLDEAYIQPQPLGVVLIIGAWNYPFVLTIQPLIGAIAAGNAVIIKPSELSENTAKILAKLLPQYLDQDLYIVINGGVEETTELLKQRFDHIFYTGNTAVGKIVMEAAAKHLTPVTLELGGKSPCYIDKDCDLDIVCRRITWGKYMNCGQTCIAPDYILCEASLQNQIVWKIKETVKEFYGENIKESPDYERIINLRHFKRILSLLEGQKIAFGGETDEATRYIAPTVLTDVDPKTKVMQEEIFGPILPIVPVKNVDEAINFINEREKPLALYVFSHNHKLIKRMIDETSSGGVTGNDVIMHFTLNSFPFGGVGSSGMGAYHGKHSFDTFSHQRPCLLKSLKREGANKLRYPPNSQSKVDWGKFFLLKRFNKEKLGLLLLTFLGIVAAVLVKAEYY
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
|
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| RND1 GTPase cycle | Homo sapiens |
| RND2 GTPase cycle | 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:139 | squamous cell papilloma | |
| DOID:14501 | Sjogren-Larsson syndrome | |
| DOID:1555 | urticaria | |
| DOID:1558 | angioedema | |
| DOID:1572 | normal pressure hydrocephalus | |
| DOID:1697 | ichthyosis | |
| DOID:1699 | obsolete congenital ichthyosiform erythroderma | |
| DOID:1826 | epilepsy | |
| DOID:1837 | diabetic ketoacidosis | |
| DOID:1969 | cerebral palsy |
