Solute carrier family 22 member 5

Solute carrier family 22 member 5

Item
http://www.wikidata.org/entity/Q7390798
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporterOCTN2-mediated carnitine uptake in a newly discovered human proximal tubule cell line (Caki-1)L-Carnitine transport in human placental brush-border membranes is mediated by the sodium-dependent organic cation transporter OCTN2The Bacillus subtilis quorum-sensing molecule CSF contributes to intestinal homeostasis via OCTN2, a host cell membrane transporterPDZK1 directly regulates the function of organic cation/carnitine transporter OCTN2Expression and localization of carnitine/organic cation transporter OCTN1 and OCTN2 in ocular epitheliumMolecular and functional identification of sodium ion-dependent, high affinity human carnitine transporter OCTN2cDNA sequence, transport function, and genomic organization of human OCTN2, a new member of the organic cation transporter family
P921

Solute carrier family 22 member 5

Item
http://www.wikidata.org/entity/Q7390798
description
humanes Protein
@de
mammalian protein found in Homo sapiens
@en
menselijk eiwit
@nl
protein
@id
protein
@sv
proteinë
@sq
protèin
@ace
protéine humaine
@fr
بروتين بشري
@ar
name
Solute carrier family 22 member 5
@en
Solute carrier family 22 member 5
@nl
type
label
Solute carrier family 22 member 5
@en
Solute carrier family 22 member 5
@nl
altLabel
High-affinity sodium-dependent carnitine cotransporter
@en
SLC22A5
@en
high-affinity sodium dependent carnitine cotransporter
@en
organic cation/carnitine transporter 2
@en
solute carrier family 22 member 5
@en
prefLabel
Solute carrier family 22 member 5
@en
Solute carrier family 22 member 5
@nl
P31
P352
P361
P527
P637
P680
P681
P682
P692
P702
P703
P705
P7260
P352
P637
P31
P352
P361
P527
P637
P680
P681
P682
P692
P702
P703
P705
P7260