NBPF15

NBPF15
Identifiers
Aliases	NBPF15, AB14, AG3, NBPF16, neuroblastoma breakpoint family member 15, NBPF member 15, MGC8902
External IDs	OMIM: 610414, 614005; HomoloGene: 41035; GeneCards: NBPF15; OMA:NBPF15 - orthologs
Gene location (Human)
Chr.	Chromosome 1 (human)
End	144,461,674 bp
RNA expression pattern
	Top expressed in
	ventricular zone; ; cerebellar hemisphere; ; thymus; ; right hemisphere of cerebellum; ; stromal cell of endometrium; ; thyroid gland; ; ganglionic eminence; ; right lobe of thyroid gland; ; left lobe of thyroid gland; ; right lobe of liver;
	n/a
	More reference expression data
	n/a
Orthologs
	284565
	n/a
	ENSG00000266338
	n/a
	Q8N660
	n/a
	NM_001102663; NM_001170755; NM_173638
	n/a
	NP_001164226; NP_775909
	n/a
	Wikidata
View/Edit Human

Neuroblastoma breakpoint family, member 15, also known as NBPF15, is a protein which in humans is encoded by the NBPF15 gene. The gene is 18762 bp long, with mRNA that is 3837 bp long. The gene is located on chromosome 1q21.1. Its sub-cellular location is predicted to be in the nucleus and cytoplasm. It contains what is known as the NBPF repeat, which is a two-exon stretch of sequence that is characteristic of all 21 members of the NBPF gene family. The repeat is considered the ancestral exons, and the NBPF family has been linked to primate evolution.