FNBP4

FNBP4
Identifiers
Aliases	FNBP4, FBP30, formin binding protein 4
External IDs	OMIM: 615265; MGI: 1860513; HomoloGene: 9087; GeneCards: FNBP4; OMA:FNBP4 - orthologs
Gene location (Human)
Chr.	Chromosome 11 (human)
End	47,767,443 bp
Gene location (Mouse)
Chr.	Chromosome 2 (mouse)
End	90,781,021 bp
RNA expression pattern
	Top expressed in
	sural nerve; ; gastric mucosa; ; Achilles tendon; ; left ovary; ; body of uterus; ; right ovary; ; canal of the cervix; ; body of pancreas; ; right uterine tube; ; left lobe of thyroid gland;
	Top expressed in
	tail of embryo; ; neural layer of retina; ; genital tubercle; ; spermatocyte; ; ventricular zone; ; zygote; ; granulocyte; ; cerebellar cortex; ; thymus; ; neural tube;
	More reference expression data
	More reference expression data
Orthologs
	23360
	55935
	ENSG00000109920; ENSG00000285182
	ENSMUSG00000008200
	Q8N3X1
	Q6ZQ03
	NM_015308; NM_001318339
	NM_018828
	NP_001305268; NP_056123
	NP_061298
	Wikidata
View/Edit Human	View/Edit Mouse

Formin-binding protein 4 is a protein that in humans is encoded by the FNBP4 gene.

Mutations in this gene have been found associated to cases similar to microphthalmia with limb anomalies (doi: 10.1002/ajmg.a.35983).