ABCA1
protein-coding gene in the species Homo sapiens
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ABCA1
Summary
ABCA1 is a gene[1].
Key Facts
- ABCA1's instance of is recorded as gene[2].
- ABCA1 is a type of protein-coding gene[3].
- ABCA1's HomoloGene ID is recorded as 21130[4].
- ABCA1's genomic start is recorded as 107543283[5].
- ABCA1's genomic start is recorded as 104781006[6].
- ABCA1's genomic end is recorded as 107690518[7].
- ABCA1's genomic end is recorded as 104928155[8].
- ABCA1's ortholog is recorded as Abca1[9].
- ABCA1's ortholog is recorded as Abca1[10].
- ABCA1's ortholog is recorded as abca1b[11].
- ABCA1's ortholog is recorded as abt-2[12].
- ABCA1's ortholog is recorded as abca1a[13].
- ABCA1's encodes is recorded as ATP binding cassette subfamily A member 1[14].
- ABCA1's found in taxon is recorded as Homo sapiens[15].
- ABCA1's chromosome is recorded as human chromosome 9[16].
- ABCA1's genetic association is recorded as myopia[17].
- ABCA1's genetic association is recorded as metabolic disease[18].
- ABCA1's genetic association is recorded as lipid metabolism disorder[19].
- ABCA1's genetic association is recorded as coronary artery disease[20].
- ABCA1's genetic association is recorded as Tangier disease[21].
- ABCA1's strand orientation is recorded as reverse strand[22].
- ABCA1's exact match is recorded as http://identifiers.org/ncbigene/19[23].
- ABCA1's cytogenetic location is recorded as 9q31.1[24].
- ABCA1's expressed in is recorded as skin of hip[25].
- ABCA1's expressed in is recorded as left adrenal gland[26].