FCHSD1

FCHSD1
Identifiers
Aliases	FCHSD1, NWK2, FCH and double SH3 domains 1
External IDs	OMIM: 617555; MGI: 2441771; HomoloGene: 14127; GeneCards: FCHSD1; OMA:FCHSD1 - orthologs
Gene location (Human)
Chr.	Chromosome 5 (human)
End	141,651,418 bp
Gene location (Mouse)
Chr.	Chromosome 18 (mouse)
End	38,102,827 bp
RNA expression pattern
	Top expressed in
	granulocyte; ; left ovary; ; Descending thoracic aorta; ; appendix; ; right ovary; ; anterior pituitary; ; ascending aorta; ; sural nerve; ; body of uterus; ; ectocervix;
	Top expressed in
	granulocyte; ; lip; ; ventricular zone; ; right kidney; ; blood; ; dentate gyrus of hippocampal formation granule cell; ; embryo; ; esophagus; ; neural layer of retina; ; primary visual cortex;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	lipid binding;
Cellular component	neuromuscular junction; recycling endosome; cuticular plate; cytoplasm; cytoplasmic vesicle; cell projection; perikaryon;
Biological process	neuromuscular synaptic transmission; regulation of actin filament polymerization; positive regulation of actin filament polymerization;
	Sources:Amigo / QuickGO
Orthologs
	89848
	319262
	ENSG00000197948
	ENSMUSG00000038524
	Q86WN1
	Q6PFY1
	NM_033449
	NM_175684
	NP_258260
	NP_783615
	Wikidata
View/Edit Human	View/Edit Mouse

FCH and double SH3 domains protein 1 is a protein that in humans is encoded by the FCHSD1 gene.