APRT
protein-coding gene in the species Homo sapiens
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APRT
Summary
APRT is a gene[1].
Key Facts
- APRT's instance of is recorded as gene[2].
- APRT is a type of protein-coding gene[3].
- APRT's HomoloGene ID is recorded as 413[4].
- APRT's genomic start is recorded as 88809339[5].
- APRT's genomic start is recorded as 88875747[6].
- APRT's genomic end is recorded as 88878352[7].
- APRT's genomic end is recorded as 88811937[8].
- APRT's ortholog is recorded as Aprt[9].
- APRT's ortholog is recorded as APT1[10].
- APRT's ortholog is recorded as Aprt[11].
- APRT's ortholog is recorded as T19B4.3[12].
- APRT's ortholog is recorded as aprt[13].
- APRT's ortholog is recorded as Aprt[14].
- APRT's encodes is recorded as Adenine phosphoribosyltransferase[15].
- APRT's found in taxon is recorded as Homo sapiens[16].
- APRT's chromosome is recorded as human chromosome 16[17].
- APRT's genetic association is recorded as adenine phosphoribosyltransferase deficiency[18].
- APRT's strand orientation is recorded as reverse strand[19].
- APRT's exact match is recorded as http://identifiers.org/ncbigene/353[20].
- APRT's cytogenetic location is recorded as 16q24.3[21].
- APRT's expressed in is recorded as skin of abdomen[22].
- APRT's expressed in is recorded as skin of leg[23].
- APRT's expressed in is recorded as granulocyte[24].
- APRT's expressed in is recorded as mucosa of transverse colon[25].
- APRT's expressed in is recorded as body of pancreas[26].