about
P527
P688
Identification and comparative functional characterization of a new human riboflavin transporter hRFT3 expressed in the brainSLC52A2 [p.P141T] and SLC52A3 [p.N21S] causing Brown-Vialetto-Van Laere Syndrome in an Indian patient: First genetically proven case with mutations in two riboflavin transportersCloning and functional characterization of a gamma-hydroxybutyrate receptor identified in the human brain.
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Solute carrier family 52 member 2
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
Solute carrier family 52 member 2
@en
type
label
Solute carrier family 52 member 2
@en
altLabel
G protein-coupled receptor 172A
@en
GHB Receptor
@en
GHBh1
@en
PERV-A receptor 1
@en
Protein GPR172A
@en
SLC52A2
@en
hRFT3
@en
porcine endogenous retrovirus A receptor 1
@en
putative G-protein coupled receptor GPCR41
@en
riboflavin transporter 3
@en
prefLabel
Solute carrier family 52 member 2
@en
P637
P680
P681
P682
P705
P352
P637
P31
P352
P637
NP_001240744
NP_001240745
NP_001350047
NP_001350049
NP_001350050
NP_001350051
XP_011515602
XP_016869310
XP_016869311
P702
P703
P705
ENSP00000333638
ENSP00000385961
ENSP00000431965
ENSP00000433583
ENSP00000433796
ENSP00000434239
ENSP00000434728
ENSP00000435820
ENSP00000436917
ENSP00000493758
P7260
2.A.125.1.3