InnateDB Protein
|
IDBP-381540.5
|
Last Modified
|
2014-10-13 [Report errors or provide feedback]
|
Gene Symbol
|
L2HGDH
|
Protein Name
|
L-2-hydroxyglutarate dehydrogenase
|
Synonyms
|
|
Species
|
Homo sapiens
|
Ensembl Protein
|
ENSP00000405559
|
InnateDB Gene
|
IDBG-5941 (L2HGDH)
|
Protein Structure
|
|
Function |
|
Subcellular Localization |
Mitochondrion {ECO:0000269PubMed:16005139}.
|
Disease Associations |
L-2-hydroxyglutaric aciduria (L2HGA) [MIM:236792]: A rare autosomal recessive disorder clinically characterized by mild psychomotor delay in the first years of life, followed by progressive cerebellar ataxia, dysarthria and moderate to severe mental retardation. Diagnosis is based on the presence of an excess of L-2-hydroxyglutaric acid in urine, blood and cerebrospinal fluid. {ECO:0000269PubMed:15385440, ECO:0000269PubMed:15548604, ECO:0000269PubMed:16134148}. Note=The disease is caused by mutations affecting the gene represented in this entry.
|
Tissue Specificity |
Widely expressed. Highly expressed in brain, testis and muscle. Expressed to a lower extent in lymphocytes, fibroblasts, keratinocytes, placenta, bladder, small intestine, liver and bone marrow. {ECO:0000269PubMed:15385440}.
|
Comments |
|
Number of Interactions
|
This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
3
[view]
|
Protein-Protein |
2
[view]
|
Protein-DNA |
1
[view]
|
Protein-RNA |
0
|
DNA-DNA |
0
|
RNA-RNA |
0
|
DNA-RNA |
0
|
|
|
|
Molecular Function |
Accession |
GO Term |
GO:0016491
|
oxidoreductase activity
|
GO:0047545
|
2-hydroxyglutarate dehydrogenase activity
|
|
Biological Process |
|
Cellular Component |
|
PDB ID |
|
InterPro |
IPR006076
FAD dependent oxidoreductase
|
PFAM |
PF01266
|
PRINTS |
|
PIRSF |
|
SMART |
|
TIGRFAMs |
|
Modification |
|
SwissProt |
Q9H9P8
|
PhosphoSite |
PhosphoSite-Q9H9P8
|
TrEMBL |
|
UniProt Splice Variant |
|
Entrez Gene |
79944
|
UniGene |
Hs.256034
|
RefSeq |
XP_005268132
|
HUGO |
HGNC:20499
|
OMIM |
609584
|
CCDS |
CCDS9698
|
HPRD |
12640
|
IMGT |
|
EMBL |
AK022680
AL109758
AL359397
AY757363
BC006117
|
GenPept |
AAH06117
AAV52330
BAB14174
|
|
|