PGM1

PGM1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPGM1, CDG1T, GSD14, phosphoglucomutase 1
External IDsOMIM: 171900; MGI: 97565; HomoloGene: 1979; GeneCards: PGM1; OMA:PGM1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

5236

72157

Ensembl

ENSG00000079739

ENSMUSG00000025791

UniProt

P36871

Q9D0F9

RefSeq (mRNA)

NM_002633
NM_001172818
NM_001172819

NM_028132

RefSeq (protein)

NP_001166289
NP_001166290
NP_002624

NP_082408

Location (UCSC)Chr 1: 63.59 – 63.66 MbChr 4: 99.93 – 99.99 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Phosphoglucomutase-1 is an enzyme that in humans is encoded by the PGM1 gene. The protein encoded by this gene is an isozyme of phosphoglucomutase (PGM) and belongs to the phosphohexose mutase family. There are several PGM isozymes, which are encoded by different genes and catalyze the transfer of phosphate between the 1 and 6 positions of glucose. In most cell types, this PGM isozyme is predominant, representing about 90% of total PGM activity. In red blood cells, PGM2 is a major isozyme. This gene is highly polymorphic. Mutations in this gene cause CDG syndrome type 1t (CDG1T, formerly known as glycogen storage disease type XIV). Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Mar 2010]