SLC25A15

Stable Identifier
R-HSA-70618
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Mitochondrial ornithine transporter 1, Solute carrier family 25, member 15
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
  The Metabolic and Molecular Bases of Inherited Disease, 8th ed

Scriver, CR, Beaudet, AL, Valle, D, Sly, WS

  2001
10369256 Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter.

Camacho, JA, Obie, C, Biery, B, Goodman, BK, Hu, CA, Almashanu, S, Steel, G, Casey, R, Lambert, M, Mitchell, GA, Valle, D

Nat Genet 1999
External Reference Information
External Reference
Gene Names
SLC25A15, ORC1, ORNT1, SP1855
Chain
chain:1-301
Reference Transcript
Other Identifiers
10166
11739956_s_at
11746530_s_at
222705_s_at
3479984
3482075
3482077
3486732
3486734
3486735
3486740
3486741
3486742
3486745
3486748
3486749
3486751
3486754
3486755
3951512
42146
62682_at
7968734
A_33_P3840512
AAD45238
AAG17977
AAH02702
AF112968
AF177333
AJ309943
AL161614
BC002702
CAC83972
CCDS9373
CH471075
EAX08630
ENSG00000102743
ENSP00000342267
ENST00000338625
EntrezGene:10166
F2Z354
g12803730_3p_a_at
GO:0000050
GO:0000064
GO:0003674
GO:0005575
GO:0005622
GO:0005623
GO:0005737
GO:0005739
GO:0005743
GO:0006810
GO:0006839
GO:0008150
GO:0009058
GO:0016020
GO:0016021
GO:0022857
GO:0034641
GO:0043226
GO:0044281
GO:0055085
GO:0071941
GO:1990575
HGNC:10985
HPA042146
ILMN_2070013
IPR018108
IPR023395
MIM:238970
MIM:603861
NM_014252
NP_055067
PF00153
Q5VZD9
SLC25A15
SLC25A15-201
TC0Y000343.hg
TC13000140.hg
uc001uxn.4
UPI0000130E9D
Participant Of
Inferred To
Cross References
RefSeq
GeneCards
PRO
Orphanet
HMDB Protein