Protein Slc25a20

URN urn:agi-llid:788
Connectivity 24
Name Slc25a20
Description solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
Notes The protein encoded by this gene is located at the mitochondrial inner membrane where it transfers fatty acylcarnitines into mitochondria. Thus it is critical in the fatty acid oxidation process. A defect in this translocase impairs oxidation of fatty acids and can cause a varieties of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness.

Pathway fatty acid beta degradation pathway

GO Molecular Function transporter activity
acyl carnitine transporter activity

GO Cellular Component membrane
mitochondrion
mitochondrial inner membrane
integral to membrane

GO Biological Process transmembrane transport
transport
regulation of fatty acid oxidation
carnitine shuttle

Ariadne Ontology Fatty acid oxidation
Lipid transport

Group Fatty acid oxidation
Lipid transport
transporter activity
transmembrane transport
transport
regulation of fatty acid oxidation
carnitine shuttle
acyl carnitine transporter activity
membrane
mitochondrion
mitochondrial inner membrane
integral to membrane

MedScan ID 788

Hugo ID 1421

Human chromosome position 3p21.31

LocusLink ID 788
57279
117035

Alias CAC
CACT
mitochondrial carnitine/acylcarnitine carrier protein
OTTHUMP00000210385
solute carrier family 25 member 20
carnitine/acylcarnitine translocase
carnitine/acylcarnitine carrier protein
mCAC
C78826
1110007P09Rik
mitochondrial carnitine-acylcarnitine translocase
MGC93269
solute carrier family 25 (mitochondrial carnitine/acylcarnitine translocase), member 20
1110007P09
carnitine-acylcarnitine carrier
Slc25a20
solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
Carnitine-acylcarnitine translocase
RIKEN cDNA 1110007P09 gene
mitochondrial carnitine-acylcarnitine translocase gene

Organism Homo sapiens
Mus musculus
Rattus norvegicus

GenBank ID NC_000003
NM_000387
NP_000378
NT_022517
NW_001838877
NW_921651
NG_008171
AC_000135
AC_000046
AC134028
CH471055
EAW64929
Y17775
CAB55356
AK301744
BAG63207
AK312962
BAG35801
BC001689
AAH01689
BI913588
BQ018220
CR607188
CR620282
DC360427
Y10319
CAA71367
O43772
DQ892599
ABM83525
DQ895828
ABM86754
NC_000075
NM_020520
NP_065266
NT_039477
NW_001030918
AC_000031
AB017112
BAA74768
AC173341
CH466560
EDL21310
CT571271
AK075624
BAC35865
AK152436
BAE31218
AK161086
AK177588
AK211911
AK215475
BC029733
AAH29733
BC052871
AAH52871
Q7TPW6
Q9Z2Z6
NC_005107
NM_053965
NP_446417
NW_047802
NW_001084876
AC_000076
CH473954
EDL77151
EDL77152
BC081749
AAH81749
X97831
CAA66410
P97521
Q66HP8

OMIM ID 212138

Mouse chromosome position 9
9 F2

GO ID 0015227
0005215
0006853
0046320
0055085
0016021
0016020
0005743
0005739
0006810
0005488
0005319
0019866

Rat chromosome position 8q32

Swiss-Prot Accession O43772
Q9Z2Z6
Q7TPW6
Q66HP8
P97521
Q3U801
B2R7F4
Q9UIQ2

Unigene ID Hs.13845
Mm.29666
Rn.3289

KEGG ID hsa:788
mmu:57279
rno:117035

Swiss-Prot ID MCAT_MOUSE
MCAT_HUMAN
Q66HP8_RAT

Cell Localization Mitochondrion inner membrane
Mitochondria
Plasma membrane

IPI ID IPI00131584
IPI00013957
IPI00471905
IPI00205413

Homologene ID 331

RGD ID 621443

MGI ID 1928738