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Protein-coding gene in the species Homo sapiens
Apolipoprotein L2 is a protein that in humans is encoded by the APOL2 gene. This gene is a member of the apolipoprotein L gene family and protein in this
APOL2
Protein family
velocardiofacial syndrome that includes symptoms of schizophrenia. APOL1; APOL2; APOL3; APOL4; APOL5; APOL6; APOLD1; Arai H, Mimmack ML, Ryan M, Baba H
Apolipoprotein_L
HGNC:615; Q13790 876 APOH HGNC:616; P02749 877 APOL1 HGNC:618; O14791 878 APOL2 HGNC:619; Q9BQE5 879 APOL3 HGNC:14868; O95236 880 APOL4 HGNC:14867; Q9BPW4
List of human protein-coding genes 1
List_of_human_protein-coding_genes_1
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