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NBPF10
Neuroblastoma breakpoint family member 10 is a protein that in ''Homo sapiens'' is encoded by the ''NBPF10'' gene.〔(【引用サイトリンク】 url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&DbFrom=protein&Cmd=Link&LinkName=protein_gene&IdsFromResult=291621653 )〕
The full gene is 75,313 bp, with the major isoform of mRNA being 10,697 bp long. The gene is located at 1q21.1. NBPF contains what is known as the DUF1220 repeats. The highly conserved, repeated region is believed to be originated from MGC8902. The NBPF family has been linked to primate evolution.〔 It is assumed to be related to the 1q21.1 deletion syndrome and 1q21.1 duplication syndrome.〔e.g.: L. Dumas and J.M. Sikela; DUF1220 Domains, Cognitive Disease, and Human Brain Evolution; Advance 2009, ; Cold Spring Harbor Laboratory Press〕
== Homology ==
Paralogs of NBPF10 includes other NBPF family members.
Orthologs of NBPF10 are found in other primates; distant orthologs are found in bovine, equine, and canine
NBPF10 paralogs and orthologs unrooted phylogenetic tree
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