about
P688
The human and mouse SLC25A29 mitochondrial transporters rescue the deficient ornithine metabolism in fibroblasts of patients with the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome.The human gene SLC25A29, of solute carrier family 25, encodes a mitochondrial transporter of basic amino acids.
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 25 member 29
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
Solute carrier family 25 member 29
@en
type
label
Solute carrier family 25 member 29
@en
altLabel
CACT-like
@en
Carnitine/acylcarnitine translocase-like
@en
SLC25A29
@en
carnitine-acylcarnitine translocase like
@en
mitochondrial basic amino acids transporter
@en
mitochondrial carnitine/acylcarnitine carrier protein CACL
@en
mitochondrial ornithine transporter 3
@en
solute carrier family 25 (mitochondrial carnitine/acylcarnitine carrier), member 29
@en
prefLabel
Solute carrier family 25 member 29
@en
P637
P680
P681
P682
P705
P352
P637
P31
P352
P637
NP_001034444
NP_001278742
NP_001278743
NP_001339749
NP_001339750
NP_001339751
NP_001339752
XP_006720101
XP_006720102
P680
P682
P702
P703
P705
ENSP00000352167
ENSP00000376640
ENSP00000450913
ENSP00000451573
ENSP00000451644
ENSP00000451808
ENSP00000451952
ENSP00000452078
ENSP00000452324
ENSP00000452446
P7260
2.A.29.8.9