SLC25A15 [mitochondrial inner membrane]

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
0000670273
10166
11739956_s_at
11746530_s_at
11756145_s_at
16774235
218653_at
222705_s_at
3479984
3482075
3482077
3486731
3486732
3486734
3486735
3486740
3486741
3486742
3486745
3486748
3486749
3486751
3486754
3486755
3486756
3486757
3486758
3951512
54978_at
62682_at
7968734
A_14_P136137
A_23_P128650
A_33_P3840512
GE58576
GO:0000050
GO:0000064
GO:0003674
GO:0005575
GO:0005622
GO:0005737
GO:0005739
GO:0005743
GO:0006810
GO:0008150
GO:0009058
GO:0016020
GO:0016021
GO:0022857
GO:0034641
GO:0043226
GO:0044281
GO:0055085
GO:0071941
GO:1990575
ILMN_1667670
ILMN_2070013
PH_hs_0004524
TC0Y000343.hg
TC13000140.hg
g12803730_3p_a_at
g7657584_3p_at
Participant Of
Inferred To
Cross References
RefSeq
OpenTargets
GeneCards
PRO
Orphanet
HMDB Protein
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