NBPF19

NBPF19
Identifiers
Aliases	NBPF19, NBPF member 19
External IDs	OMIM: 614006; HomoloGene: 41035; GeneCards: NBPF19; OMA:NBPF19 - orthologs
Gene location (Human)
Chr.	Chromosome 1 (human)
End	149,556,361 bp
RNA expression pattern
	Top expressed in
	sural nerve; ; bone marrow cells; ; monocyte; ; epithelium of colon; ; ventricular zone; ; granulocyte; ; Achilles tendon; ; tonsil; ; gastric mucosa; ; stromal cell of endometrium;
	n/a
	More reference expression data
	n/a
Gene ontology
Molecular function	calcium ion binding; protein binding; Notch binding;
Cellular component	cytoplasm; extracellular region; plasma membrane;
Biological process	Notch signaling pathway; multicellular organism development; cell differentiation; cerebral cortex development; positive regulation of Notch signaling pathway;
	Sources:Amigo / QuickGO
Orthologs
	101060226
	n/a
	ENSG00000271383
	n/a
	Q7Z3S9
	n/a
	NM_001351365
	n/a
	NP_001350936; NP_001350937
	n/a
	Wikidata
View/Edit Human

Neuroblastoma breakpoint family member 19, or NBPF19, is a protein that in humans is encoded by the NBPF19 gene. This protein is included in the neuroblastoma breakpoint family of proteins.