Phosphoglucomutase 3

 Phosphoacetylglucosamine mutase is an enzyme that in humans is encoded by the PGM3 gene.^[4][5][6]

PGM3
Identifiers
Aliases	PGM3, AGM1, IMD23, PAGM, PGM 3, Phosphoglucomutase 3
External IDs	OMIM: 172100 MGI: 97566 HomoloGene: 9205 GeneCards: PGM3
Gene location (Human) Chr. Chromosome 6 (human)[1] Band 6q14.1 Start 83,161,150 bp[1] End 83,193,936 bp[1]
RNA expression pattern More reference expression data
Gene ontology Molecular function • intramolecular transferase activity, phosphotransferases • phosphoglucomutase activity • isomerase activity • magnesium ion binding • metal ion binding • phosphoacetylglucosamine mutase activity Cellular component • cytosol • cellular component Biological process • UDP-N-acetylglucosamine biosynthetic process • protein O-linked glycosylation • glucosamine metabolic process • protein N-linked glycosylation • glucose 1-phosphate metabolic process • organic substance metabolic process • spermatogenesis • carbohydrate metabolic process • haematopoiesis Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	5238	109785
Ensembl	ENSG00000013375	ENSMUSG00000056131
UniProt	O95394	Q9CYR6
RefSeq (mRNA)	NM_001199917 NM_001199918 NM_001199919 NM_015599 NM_001367286 NM_001367287	NM_001163746 NM_028352
RefSeq (protein)	NP_001186846 NP_001186847 NP_001186848 NP_056414 NP_001354215 NP_001354216	NP_001157218 NP_082628
Location (UCSC)	Chr 6: 83.16 – 83.19 Mb	n/a
PubMed search	[2]	[3]
Wikidata
View/Edit Human View/Edit Mouse

Clinical significanceEdit

Mutations in PGM3 are associated to congenital disorder of glycosylation.^[7]

This article uses material from the Wikipedia article  Metasyntactic variable, which is released under the  Creative Commons Attribution-ShareAlike 3.0 Unported License.