ALDH18A1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 10[13]
- Cytogenetic location
- 10q24.1[20]
- Expressed in
- parotid gland, jejunal mucosa, mucosa of ileum, tibia, duodenum, rectum, mucosa of colon, mucosa of transverse colon, mucosa of sigmoid colon, secondary oocyte[21][22][23][24][25][26][27][28][29][30]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- autosomal dominant cutis laxa 3, hereditary spastic paraplegia 9A, autosomal recessive complex spastic paraplegia type 9B, autosomal dominant spastic paraplegia type 9, autosomal dominant cutis laxa[14][15][16][17][18]
- HomoloGene ID
- 2142[3]
- Strand orientation
- reverse strand[19]
🏷️ Also known as
en ADCL3
en aldehyde dehydrogenase 18 family member A1
en Aldehyde dehydrogenase 18 family, member A1
en ALDH18A1
en ARCL3A
en GSAS
en P5CS
en PYCS
en SPG9
en SPG9A
en SPG9B
🔖 Identifiers · 11
- Image (Wikimedia Commons)
- Protein ALDH18A1 PDB 2h5g.png ↗
- Ensembl gene ID
- ENSG00000059573
- Ensembl transcript ID
- ENST00000489386, ENST00000371221, ENST00000371224, ENST00000483788, ENST00000485428
- Entrez Gene ID
- 5832
- Exact match
- identifiers.org
- Freebase ID
- /m/03hmfgg
- HGNC ID
- 9722
- HGNC gene symbol
- ALDH18A1
- OMIM ID
- 138250
- RefSeq RNA ID
- NM_001017423, NM_002860, NM_001323412, NM_001323413, NM_001323414, NM_001323415, NM_001323416, NM_001323417, NM_001323418, NM_001323419
- UMLS CUI
- C1538262
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