UGDH (UDP-glucose 6-dehydrogenase)

2010-02-01  

Identity

HGNC
LOCATION
4p14
LOCUSID
ALIAS
DEE84,EIEE84,GDH,UDP-GlcDH,UDPGDH,UGD
FUSION GENES

Other Information

Locus ID:

NCBI: 7358
MIM: 603370
HGNC: 12525
Ensembl: ENSG00000109814

Variants:

dbSNP: 7358
ClinVar: 7358
TCGA: ENSG00000109814
COSMIC: UGDH

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000109814ENST00000316423O60701
ENSG00000109814ENST00000501493O60701
ENSG00000109814ENST00000503779E9PBD2
ENSG00000109814ENST00000505698E7ER95
ENSG00000109814ENST00000506179O60701
ENSG00000109814ENST00000507089O60701
ENSG00000109814ENST00000509391E7ER83
ENSG00000109814ENST00000510490D6RHF4
ENSG00000109814ENST00000510881E9PBD2
ENSG00000109814ENST00000514106E7ETF4
ENSG00000109814ENST00000515021E7EV97

Expression (GTEx)

0
10
20
30
40
50
60
70
80
90

Pathways

PathwaySourceExternal ID
Pentose and glucuronate interconversionsKEGGko00040
Ascorbate and aldarate metabolismKEGGko00053
Amino sugar and nucleotide sugar metabolismKEGGko00520
Pentose and glucuronate interconversionsKEGGhsa00040
Ascorbate and aldarate metabolismKEGGhsa00053
Amino sugar and nucleotide sugar metabolismKEGGhsa00520
Metabolic pathwaysKEGGhsa01100
Nucleotide sugar biosynthesis, eukaryotesKEGGhsa_M00361
Glucuronate pathway (uronate pathway)KEGGM00014
Nucleotide sugar biosynthesis, eukaryotesKEGGM00361
Glucuronate pathway (uronate pathway)KEGGhsa_M00014
MetabolismREACTOMER-HSA-1430728
Biological oxidationsREACTOMER-HSA-211859
Phase II conjugationREACTOMER-HSA-156580
GlucuronidationREACTOMER-HSA-156588
Formation of the active cofactor, UDP-glucuronateREACTOMER-HSA-173599

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
375939992023Phenotypic and genetic characteristics of 24 cases of early infantile epileptic encephalopathy in East China, including a rare case of biallelic UGDH mutations.1
378581592023UGDH promotes tumor-initiating cells and a fibroinflammatory tumor microenvironment in ovarian cancer.2
375939992023Phenotypic and genetic characteristics of 24 cases of early infantile epileptic encephalopathy in East China, including a rare case of biallelic UGDH mutations.1
378581592023UGDH promotes tumor-initiating cells and a fibroinflammatory tumor microenvironment in ovarian cancer.2
356178082022UDP-glucose 6-dehydrogenase lessens sorafenib sensitivity via modulating unfolded protein response.2
356178082022UDP-glucose 6-dehydrogenase lessens sorafenib sensitivity via modulating unfolded protein response.2
327499012021Integration of Sugar Metabolism and Proteoglycan Synthesis by UDP-glucose Dehydrogenase.16
327499012021Integration of Sugar Metabolism and Proteoglycan Synthesis by UDP-glucose Dehydrogenase.16
313084902020UDP-glucose 6-dehydrogenase regulates hyaluronic acid production and promotes breast cancer progression.30
320017162020Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.26
327685252020UDP-glucose 6-dehydrogenase knockout impairs migration and decreases in vivo metastatic ability of breast cancer cells.17
328939772020Targeting UDP-glucose dehydrogenase inhibits ovarian cancer growth and metastasis.10
313084902020UDP-glucose 6-dehydrogenase regulates hyaluronic acid production and promotes breast cancer progression.30
320017162020Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.26
327685252020UDP-glucose 6-dehydrogenase knockout impairs migration and decreases in vivo metastatic ability of breast cancer cells.17

Citation

Dessen P

UGDH (UDP-glucose 6-dehydrogenase)

Atlas Genet Cytogenet Oncol Haematol. 2010-02-01

Online version: http://atlasgeneticsoncology.org/gene/51337