about
P688
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBATDifferential influence of the 4F2 heavy chain and the protein related to b(0,+) amino acid transport on substrate affinity of the heteromeric b(0,+) amino acid transporterrBAT-b(0,+)AT heterodimer is the main apical reabsorption system for cystine in the kidneyA novel missense mutation of SLC7A9 frequent in Japanese cystinuria cases affecting the C-terminus of the transporter
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 7 member 9
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
Solute carrier family 7 member 9
@en
type
label
Solute carrier family 7 member 9
@en
altLabel
B(0,+)-type amino acid transporter 1
@en
SLC7A9
@en
b(0,+)AT
@en
glycoprotein-associated amino acid transporter b0,+AT1
@en
solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9
@en
solute carrier family 7 (cationic amino acid transporter, y+ system), member 9
@en
solute carrier family 7 (glyco ...... chain, bo,+ system), member 9
@en
prefLabel
Solute carrier family 7 member 9
@en
P637
P680
P681
P682
P705
P352
P31
P352
P637
NP_001119807
NP_001229965
XP_006723055
XP_011524704
XP_016881719
XP_024307102
P680
P681
P682
P702
P703
P705
ENSP00000023064
ENSP00000464822
ENSP00000465563
ENSP00000468076
ENSP00000468439
P7260
2.A.3.8.19