about
P527
P688
Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotypeSubstitution p.A350V in Na⁺/Mg²⁺ exchanger SLC41A1, potentially associated with Parkinson's disease, is a gain-of-function mutationSLC41A1 is a novel mammalian Mg2+ carrierHuman gene SLC41A1 encodes for the Na+/Mg²+ exchangerSLC41A1 Mg(2+) transport is regulated via Mg(2+)-dependent endosomal recycling through its N-terminal cytoplasmic domain.
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
proteinë
@sq
proteïne in Solute carrier family 41 member 1
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
Solute carrier family 41 member 1
@en
type
label
Solute carrier family 41 member 1
@en
altLabel
SLC41A1
@en
solute carrier family 41 (magnesium transporter), member 1
@en
solute carrier family 41 member 1
@en
prefLabel
Solute carrier family 41 member 1
@en
P680
P681
P682
P352
P31
P352
P637
XP_005245126
P680
P681
P682
P702
P703
P705
ENSP00000356105
P7260
1.A.26.2.1