Spermatogenesis associated 13

SPATA13
Identifiers
Aliases	SPATA13, ARHGEF29, ASEF2, spermatogenesis associated 13
External IDs	OMIM: 613324; MGI: 104838; HomoloGene: 19482; GeneCards: SPATA13; OMA:SPATA13 - orthologs
Gene location (Mouse)
Chr.	Chromosome 14 (mouse)
End	61,002,005 bp
Gene ontology
Molecular function	protein binding; guanyl-nucleotide exchange factor activity; identical protein binding;
Cellular component	cytoplasm; filopodium; ruffle membrane; plasma membrane; cell projection; membrane; lamellipodium; nucleoplasm; cytosol;
Biological process	filopodium assembly; regulation of Rho protein signal transduction; regulation of cell migration; cell migration; lamellipodium assembly;
	Sources:Amigo / QuickGO
Orthologs
	221178
	219140
	n/a
	ENSMUSG00000021990
	Q96N96
	Q5DU57
NM_001166271; NM_001286792; NM_001286793; NM_001286794; NM_001286795;
	NM_153023
	NM_001033272; NM_001310594
NP_001159743; NP_001273721; NP_001273722; NP_001273723; NP_001273724;
	NP_694568; NP_694568.1
NP_001028444; NP_001297523; NP_001391878; NP_001391879; NP_001391880;
	NP_001391881; NP_001391882; NP_001391883; NP_001391893
	Wikidata
View/Edit Human	View/Edit Mouse

Spermatogenesis associated 13 is a protein that in humans is encoded by the SPATA13 gene.