NBPF10

NBPF20
Identifiers
Aliases	NBPF20, NBPF member 20
External IDs	OMIM: 614007; HomoloGene: 41035; GeneCards: NBPF20; OMA:NBPF20 - orthologs
Gene location (Human)
Chr.	Chromosome 1 (human)
End	145,405,567 bp
RNA expression pattern
	Top expressed in
	sural nerve; ; cerebellar cortex; ; cerebellar hemisphere; ; right hemisphere of cerebellum; ; testicle; ; stromal cell of endometrium; ; tonsil; ; bone marrow cells; ; liver; ; gonad;
	n/a
	More reference expression data
	n/a
Orthologs
	100288142
	n/a
	ENSG00000162825
	n/a
	P0DPF3; P0DPF2
	n/a
	NM_001278267; NM_001397211
	n/a
	NP_001032764; NP_001264373; NP_001265196
	n/a
	Wikidata
View/Edit Human

Neuroblastoma breakpoint family member 10 is a protein that in Homo sapiens is encoded by the NBPF10 gene.

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.