InnateDB Protein
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IDBP-477676.4
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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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GLYCTK
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Protein Name
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glycerate kinase
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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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ENSP00000418951
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InnateDB Gene
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IDBG-38597 (GLYCTK)
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Protein Structure
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Function |
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Subcellular Localization |
Isoform 1: Cytoplasm.Isoform 2: Cytoplasm. Mitochondrion.
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Disease Associations |
D-glyceric aciduria (D-GA) [MIM:220120]: A rare metabolic disease characterized by chronic metabolic acidosis and a highly variable clinical phenotype. Clinical features range from an encephalopathic presentation with seizures, microcephaly, severe mental retardation and early death, to milder manifestations with only speech delay or even normal development. {ECO:0000269PubMed:20949620}. Note=The disease is caused by mutations affecting the gene represented in this entry.
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Tissue Specificity |
Widely expressed. {ECO:0000269PubMed:16753811}.
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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 4 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
4
[view]
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Protein-Protein |
3
[view]
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Protein-DNA |
1
[view]
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
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PFAM |
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PRINTS |
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PIRSF |
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SMART |
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TIGRFAMs |
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Modification |
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SwissProt |
Q8IVS8
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PhosphoSite |
PhosphoSite-Q8IVS8
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TrEMBL |
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UniProt Splice Variant |
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Entrez Gene |
132158
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UniGene |
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RefSeq |
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HUGO |
HGNC:24247
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OMIM |
610516
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CCDS |
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HPRD |
13586
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IMGT |
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EMBL |
AF448855
AK074215
AY134474
AY172690
AY189286
AY295075
BC021896
BC036862
BC042151
DQ352863
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GenPept |
AAH21896
AAH36862
AAH42151
AAM95456
AAO17719
AAO86730
AAP41923
AAP51132
ABD22985
BAB85018
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