InnateDB Protein
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IDBP-386405.4
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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MMADHC
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Protein Name
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methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
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Synonyms
|
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000408331
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InnateDB Gene
|
IDBG-71964 (MMADHC)
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Protein Structure
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|
Function |
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Subcellular Localization |
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Disease Associations |
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Tissue Specificity |
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
1
[view]
|
Protein-Protein |
1
[view]
|
Protein-DNA |
0
|
Protein-RNA |
0
|
DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
|
|
|
|
Molecular Function |
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Biological Process |
|
Cellular Component |
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PDB ID |
|
InterPro |
IPR019362
Methylmalonic aciduria and homocystinuria type D protein
|
PFAM |
PF10229
|
PRINTS |
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PIRSF |
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SMART |
|
TIGRFAMs |
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Modification |
|
SwissProt |
|
PhosphoSite |
PhosphoSite-
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TrEMBL |
F8WEC0
|
UniProt Splice Variant |
|
Entrez Gene |
27249
|
UniGene |
Hs.602247
|
RefSeq |
|
HUGO |
HGNC:25221
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OMIM |
611935
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CCDS |
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HPRD |
10781
|
IMGT |
|
EMBL |
AC110782
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GenPept |
|
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