OTC M205V [mitochondrial matrix]

Stable Identifier
R-HSA-9957938
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
11117428 Mutation detection in 65 families with a possible diagnosis of ornithine carbamoyltransferase deficiency including 14 novel mutations

Genet, S, Cranston, T, Middleton-Price, HR

J Inherit Metab Dis 2000
External Reference Information
External Reference
Gene Names
OTC
Chain
transit peptide:1-32, chain:33-354
Other Identifiers
11740020_at
17102592
207200_PM_at
207200_at
35111_at
3973971
3973972
3973973
3973974
3973975
3973976
3973979
3973984
3973985
3973986
3973987
3973988
3973994
3973995
3973996
3973997
3973998
3973999
3974000
5009
683_at
8166769
A_14_P118950
A_23_P257355
GE57536
GO:0000050
GO:0001889
GO:0004585
GO:0005543
GO:0005739
GO:0005743
GO:0005759
GO:0006520
GO:0006526
GO:0006591
GO:0006593
GO:0007494
GO:0008652
GO:0009410
GO:0010043
GO:0016597
GO:0016740
GO:0016743
GO:0019240
GO:0031667
GO:0032868
GO:0042301
GO:0042450
GO:0042802
GO:0048856
GO:0055081
GO:0070781
GO:0071941
GO:0097272
HMNXSV003032799
ILMN_1749114
K02100_at
PH_hs_0006412
TC0X000177.hg
g9257233_3p_at
Participates
Other forms of this molecule
Modified Residues
Name
L-methionine 205 replaced with L-valine
Coordinate
205
PsiMod
A protein modification that effectively converts a source amino acid residue to an L-valine.
A protein modification that effectively removes or replaces an L-methionine.
Disease
Name Identifier Synonyms
ornithine carbamoyltransferase deficiency DOID:9271 ornithine transcarbamylase deficiency, deficiency of citrulline phosphorylase
Cross References
ClinGen
OpenTargets
Mondo
ZINC - Substances
ZINC - Biogenic
ZINC target
PRO
PDB
ZINC - Metabolites
IntEnz
GeneCards
OTC
Pharos - Targets
Orphanet
OTC
ZINC - Predictions - Purchasable
HMDB Protein
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