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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 |
|---|
| cytoplasm |
| intracellular membrane-bounded organelle |
| peroxisome |
| cytosol |
| endoplasmic reticulum membrane |
| peroxisomal membrane |
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:11830 | myopia | |
| DOID:0050572 | cone-rod dystrophy | |
| DOID:0050576 | Senior-Loken syndrome | |
| DOID:0050635 | alternating hemiplegia of childhood | |
| DOID:0060216 | Cogan syndrome | |
| DOID:0060249 | scoliosis | |
| DOID:0060640 | ethylmalonic encephalopathy | |
| DOID:0060655 | autosomal recessive congenital ichthyosis | |
| DOID:0060656 | autosomal recessive congenital ichthyosis 1 | |
| DOID:0060710 | autosomal recessive congenital ichthyosis 2 |
