SACM1L

SACM1L
Identifiers
Aliases	SACM1L, SAC1, SAC1 suppressor of actin mutations 1-like (yeast), SAC1 suppressor of actin mutations 1 like (yeast), SAC1 like phosphatidylinositide phosphatase
External IDs	OMIM: 606569; MGI: 1933169; HomoloGene: 6320; GeneCards: SACM1L; OMA:SACM1L - orthologs
Gene location (Human)
Chr.	Chromosome 3 (human)
End	45,745,409 bp
Gene location (Mouse)
Chr.	Chromosome 9 (mouse)
End	123,421,665 bp
RNA expression pattern
	Top expressed in
	secondary oocyte; ; Brodmann area 23; ; lateral nuclear group of thalamus; ; pars reticulata; ; endothelial cell; ; pars compacta; ; Epithelium of choroid plexus; ; visceral pleura; ; lower lobe of lung; ; renal medulla;
	Top expressed in
	deep cerebellar nuclei; ; medial vestibular nucleus; ; facial motor nucleus; ; substantia nigra; ; dorsal tegmental nucleus; ; pontine nuclei; ; lateral geniculate nucleus; ; mammillary body; ; Epithelium of choroid plexus; ; Paneth cell;
	More reference expression data
	n/a
Gene ontology
Molecular function	phosphatase activity; phosphoric ester hydrolase activity; phosphatidylinositol bisphosphate phosphatase activity; protein binding; hydrolase activity; phosphatidylinositol-4-phosphate phosphatase activity; phosphatidylinositol-3-phosphatase activity; phosphatidylinositol phosphate 4-phosphatase activity;
Cellular component	integral component of membrane; Golgi membrane; integral component of endoplasmic reticulum membrane; Golgi apparatus; AMPA glutamate receptor complex; endoplasmic reticulum membrane; endoplasmic reticulum; membrane;
Biological process	phosphatidylinositol biosynthetic process; phosphatidylinositol dephosphorylation;
	Sources:Amigo / QuickGO
Orthologs
	22908
	83493
	ENSG00000211456
	ENSMUSG00000025240
	Q9NTJ5
	Q9EP69
	NM_014016; NM_001319072; NM_001319073; NM_001319071
	NM_030692; NM_001357485
	NP_001306001; NP_001306002; NP_054735; NP_001306000
	NP_109617; NP_001344414
	Wikidata
View/Edit Human	View/Edit Mouse

Phosphatidylinositide phosphatase SAC1 is an enzyme that in humans is encoded by the SACM1L gene.