APOA1
protein-coding gene in the species Homo sapiens
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APOA1
Summary
APOA1 is a gene[1].
Key Facts
- APOA1's instance of is recorded as gene[2].
- APOA1 is a type of protein-coding gene[3].
- APOA1's HomoloGene ID is recorded as 47900[4].
- APOA1's genomic start is recorded as 116835751[5].
- APOA1's genomic start is recorded as 116706467[6].
- APOA1's genomic end is recorded as 116708666[7].
- APOA1's genomic end is recorded as 116837622[8].
- APOA1's ortholog is recorded as Apoa1[9].
- APOA1's ortholog is recorded as Apoa1[10].
- APOA1's ortholog is recorded as apoa1b[11].
- APOA1's ortholog is recorded as apoa1a[12].
- APOA1's encodes is recorded as Apolipoprotein A1[13].
- APOA1's encodes is recorded as Apolipoprotein A-I, isoform CRA_a[14].
- APOA1's found in taxon is recorded as Homo sapiens[15].
- APOA1's chromosome is recorded as human chromosome 11[16].
- APOA1's genetic association is recorded as hypertrophic pyloric stenosis[17].
- APOA1's genetic association is recorded as Tangier disease[18].
- APOA1's genetic association is recorded as familial visceral amyloidosis[19].
- APOA1's strand orientation is recorded as reverse strand[20].
- APOA1's exact match is recorded as http://identifiers.org/ncbigene/335[21].
- APOA1's cytogenetic location is recorded as 11q23.3[22].
- APOA1's expressed in is recorded as jejunal mucosa[23].
- APOA1's expressed in is recorded as right lobe of liver[24].
- APOA1's expressed in is recorded as mucosa of ileum[25].
- APOA1's expressed in is recorded as right testis[26].