PCSK9
protein-coding gene in the species Homo sapiens
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PCSK9
Summary
PCSK9 is a gene[1].
Key Facts
- PCSK9's instance of is recorded as gene[2].
- PCSK9 is a type of protein-coding gene[3].
- PCSK9's HomoloGene ID is recorded as 17790[4].
- PCSK9's genomic start is recorded as 55505221[5].
- PCSK9's genomic start is recorded as 55039447[6].
- PCSK9's genomic end is recorded as 55064852[7].
- PCSK9's genomic end is recorded as 55530525[8].
- PCSK9's ortholog is recorded as Pcsk9[9].
- PCSK9's ortholog is recorded as Pcsk9[10].
- PCSK9's ortholog is recorded as YSP3[11].
- PCSK9's ortholog is recorded as pcsk9[12].
- PCSK9's encodes is recorded as Proprotein convertase subtilisin/kexin type 9[13].
- PCSK9's found in taxon is recorded as Homo sapiens[14].
- PCSK9's chromosome is recorded as human chromosome 1[15].
- PCSK9's genetic association is recorded as hypercholesterolemia, autosomal dominant, 3[16].
- PCSK9's genetic association is recorded as familial hypercholesterolemia[17].
- PCSK9's strand orientation is recorded as forward strand[18].
- PCSK9's exact match is recorded as http://identifiers.org/ncbigene/255738[19].
- PCSK9's cytogenetic location is recorded as 1p32.3[20].
- PCSK9's expressed in is recorded as right lobe of liver[21].
- PCSK9's expressed in is recorded as mucosa of transverse colon[22].
- PCSK9's expressed in is recorded as testicle[23].
- PCSK9's expressed in is recorded as cerebellar hemisphere[24].
- PCSK9's expressed in is recorded as right hemisphere of cerebellum[25].
- PCSK9's expressed in is recorded as secondary oocyte[26].