ALDH18A1
protein-coding gene in the species Homo sapiens
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ALDH18A1
Summary
ALDH18A1 is a gene[1]. ALDH18A1 ranks in the top 2% of gene entities by monthly Wikipedia readership (12 views/month).[2]
Key Facts
- ALDH18A1's instance of is recorded as gene[3].
- ALDH18A1 is a type of protein-coding gene[4].
- ALDH18A1's HomoloGene ID is recorded as 2142[5].
- ALDH18A1's genomic start is recorded as 97365696[6].
- ALDH18A1's genomic start is recorded as 95605941[7].
- ALDH18A1's genomic end is recorded as 97416463[8].
- ALDH18A1's genomic end is recorded as 95656711[9].
- ALDH18A1's ortholog is recorded as Aldh18a1[10].
- ALDH18A1's ortholog is recorded as alh-13[11].
- ALDH18A1's ortholog is recorded as CG7470[12].
- ALDH18A1's ortholog is recorded as aldh18a1[13].
- ALDH18A1's ortholog is recorded as Aldh18a1[14].
- ALDH18A1's encodes is recorded as Aldehyde dehydrogenase 18 family member A1[15].
- ALDH18A1's found in taxon is recorded as Homo sapiens[16].
- ALDH18A1's chromosome is recorded as human chromosome 10[17].
- ALDH18A1's genetic association is recorded as autosomal dominant cutis laxa 3[18].
- ALDH18A1's genetic association is recorded as hereditary spastic paraplegia 9A[19].
- ALDH18A1's genetic association is recorded as autosomal recessive complex spastic paraplegia type 9B[20].
- ALDH18A1's genetic association is recorded as autosomal dominant spastic paraplegia type 9[21].
- ALDH18A1's genetic association is recorded as autosomal dominant cutis laxa[22].
- ALDH18A1's strand orientation is recorded as reverse strand[23].
- ALDH18A1's exact match is recorded as http://identifiers.org/ncbigene/5832[24].
- ALDH18A1's cytogenetic location is recorded as 10q24.1[25].
- ALDH18A1's expressed in is recorded as parotid gland[26].
- ALDH18A1's expressed in is recorded as jejunal mucosa[27].
Why It Matters
ALDH18A1 ranks in the top 2% of gene entities by monthly Wikipedia readership (12 views/month).[2]