MFSD2A

MFSD2A
Identifiants
Alias	MFSD2A
IDs externes	OMIM: 614397 MGI: 1923824 HomoloGene: 19229 GeneCards: MFSD2A
Position du gène (humain)
Chr.	Chromosome 1 humain
Fin	39,969,968 bp
Position du gène (souris)
Chr.	Chromosome 4 (souris)
Fin	122,854,981 bp
Expression génique
	Fortement exprimé dans
	right lobe of liver; ; skin of abdomen; ; mucosa of ileum; ; skin of leg; ; vésicule séminale; ; skin of arm; ; corpus epididymis; ; right testis; ; left testis; ; upper lobe of left lung;
	Fortement exprimé dans
	primary oocyte; ; zygote; ; organe otolithique; ; utricle; ; right kidney; ; epithelium of lens; ; nerf ischiatique; ; gyrus frontal supérieur; ; secondary oocyte; ; cortex visuel;
	Plus de données d'expression de référence
	n/a
Gene Ontology
Fonction moléculaire	symporter activity; phospholipid transporter activity; fatty acid transmembrane transporter activity; lysophospholipid:sodium symporter activity; transporter activity;
Composant cellulaire	integral component of membrane; integral component of plasma membrane; membrane du réticulum endoplasmique; réticulum endoplasmique; membrane; membrane plasmique;
Processus biologique	lipid transport; fatty acid transport; transcytose; lipid transport across blood-brain barrier; transport transmembranaire; establishment of blood-brain barrier; phosphatidylcholine biosynthetic process; hippocampus development; lysophospholipid transport; carbohydrate transport; organic substance transport;
	Sources:Amigo / QuickGO
Orthologues
	84879
	76574
	ENSG00000168389
	ENSMUSG00000028655
	Q8NA29; Q5SSK0
	Q9DA75
NM_001136493; NM_001287808; NM_001287809; NM_032793; NM_001349821;
	NM_001349822; NM_001349823
	NM_029662
NP_001129965; NP_001274737; NP_001274738; NP_116182; NP_001336750;
	NP_001336751; NP_001336752
	NP_083938
	Wikidata
Voir/Editer Humain	Voir/Editer Souris