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

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

Nat Genet 1999
  The Metabolic and Molecular Bases of Inherited Disease, 8th ed

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

  2001
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_PM_at
218653_at
222705_PM_s_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:0005215
GO:0005622
GO:0005737
GO:0005739
GO:0005743
GO:0015189
GO:0015297
GO:0016020
GO:0016021
GO:0022857
GO:0043226
GO:0055085
GO:0061459
GO:0071941
GO:1903401
GO:1903826
GO:1990575
HMNXSV003021904
HMNXSV003053627
ILMN_1667670
ILMN_2070013
PH_hs_0004524
TC0Y000343.hg
TC13000140.hg
g12803730_3p_a_at
g7657584_3p_at
Participates
Inferred To
Cross References
RefSeq
Guide to Pharmacology - Targets
OpenTargets
GeneCards
PRO
Pharos - Targets
Orphanet
HMDB Protein
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