MMACHC R132* [cytosol]

Stable Identifier
R-HSA-3318572
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Methylmalonic aciduria and homocystinuria type C protein, MMAC_HUMAN, MMACHC
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
MMACHC
Chain
chain:1-282
Other Identifiers
0004560603
11725013_at
1566084_at
16664091
211774_s_at
2334353
2334355
2334356
2334357
2334358
2334359
2334360
2334361
2334362
2334363
2334364
2334365
2334366
2334367
2334368
2334369
2334371
25974
37832_at
7901102
A_23_P418282
A_24_P83586
A_33_P3390643
GE900201
GO:0003674
GO:0005515
GO:0005575
GO:0005622
GO:0005737
GO:0005829
GO:0006749
GO:0006790
GO:0008150
GO:0009235
GO:0016491
GO:0016740
GO:0031419
GO:0032451
GO:0033787
GO:0034641
GO:0042803
GO:0043167
GO:0043295
GO:0044281
GO:0051186
GO:0055114
GO:0070988
GO:0071949
Hs2.33074.1.S1_3p_at
ILMN_1803005
PH_hs_0001253
TC01000573.hg
g13543966_3p_s_at
Participant Of
Other forms of this molecule
Modified Residues
Name
L-arginine 132 replaced with unknown
Coordinate
132
PsiMod
A protein modification that effectively removes or replaces an L-arginine.
Disease
Name Identifier Synonyms
methylmalonic aciduria and homocystinuria type cblC 0050715 Cobalamin C deficiency
Cross References
OpenTargets
GeneCards
PRO
Orphanet
HMDB Protein
PDB
Cite Us!