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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
aldehyde dehydrogenase 5 family member A1
Summary
- Gene Symbol
-
- ALDH5A1
- Aliases
-
- SSADH
- SSDH
- succinate-semialdehyde dehydrogenase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Disease variant
- Disulfide bond
- Mitochondrion
- NAD
- Oxidoreductase
- Phosphoprotein
- Reference proteome
- Transit peptide
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| synaptic transmission, GABAergic | ||
| succinate metabolic process | ||
| central nervous system development | ||
| post-embryonic development | ||
| glutamate metabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| synapse | ||
| mitochondrial matrix |
|
|
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| succinate-semialdehyde dehydrogenase (NAD+) activity | ||
| identical protein binding |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:12849 | autistic disorder | |
| DOID:14320 | generalized anxiety disorder | |
| DOID:1824 | status epilepticus | |
| DOID:1826 | epilepsy | |
| DOID:1827 | idiopathic generalized epilepsy | |
| DOID:2007 | degeneration of macula and posterior pole | |
| DOID:2030 | anxiety disorder | |
| DOID:2394 | ovarian cancer | |
| DOID:2468 | psychotic disorder | |
| DOID:305 | carcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000496 | Abnormality of eye movement |
| HP:0000708 | Atypical behavior |
| HP:0000709 | Psychosis |
| HP:0000717 | Autism |
| HP:0000718 | Aggressive behavior |
| HP:0000738 | Hallucinations |
| HP:0000739 | Anxiety |
| HP:0000750 | Delayed speech and language development |
| HP:0000752 | Hyperactivity |
| Disease ID | Disease Name |
|---|---|
| OMIM:271980 |
|
| ORPHA:22 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 102082621 | ORENI01879 | ||
| 108719155 | Xenbase:XB-GENE-6489369 | ||
| 108720127 | Xenbase:XB-GENE-17346769 | ||
| 100216127 | Xenbase:XB-GENE-1013005 | ||
| 101945488 | CHRPI01210 | ||
| 113435584 | PSETE06303 | ||
| 114807396 | ORNAN30071 | ||
| 103116064 | ERIEU13499 | ||
| 100411976 | CALJA31179 | ||
| 105572617 | CERAT09610 |
