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Pgm3 phosphoglucomutase 3 [ Rattus norvegicus (Norway rat) ]

Gene ID: 363109, updated on 13-Apr-2024

Summary

Official Symbol
Pgm3provided by RGD
Official Full Name
phosphoglucomutase 3provided by RGD
Primary source
RGD:1305221
See related
Ensembl:ENSRNOG00000009515 AllianceGenome:RGD:1305221
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Rattus norvegicus
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus
Summary
Predicted to enable phosphoacetylglucosamine mutase activity and phosphoglucomutase activity. Predicted to be involved in UDP-N-acetylglucosamine biosynthetic process; hemopoiesis; and protein glycosylation. Predicted to act upstream of or within glucose 1-phosphate metabolic process and spermatogenesis. Human ortholog(s) of this gene implicated in immunodeficiency 23 and teratoma. Orthologous to human PGM3 (phosphoglucomutase 3). [provided by Alliance of Genome Resources, Apr 2022]
Expression
Biased expression in Kidney (RPKM 100.0), Brain (RPKM 71.9) and 9 other tissues See more
Orthologs
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Genomic context

See Pgm3 in Genome Data Viewer
Location:
8q31
Exon count:
12
Annotation release Status Assembly Chr Location
RS_2024_02 current GRCr8 (GCF_036323735.1) 8 NC_086026.1 (96398331..96416045, complement)
RS_2023_06 previous assembly mRatBN7.2 (GCF_015227675.2) 8 NC_051343.1 (87518317..87536021, complement)
106 previous assembly Rnor_6.0 (GCF_000001895.5) 8 NC_005107.4 (94225513..94243230, complement)

Chromosome 8 - NC_086026.1Genomic Context describing neighboring genes Neighboring gene ubiquitin protein ligase E3D Neighboring gene stathmin-like Neighboring gene DOP1 leucine zipper like protein A Neighboring gene RWD domain containing 2A Neighboring gene malic enzyme 1

Genomic regions, transcripts, and products

Expression

  • Project title: A rat RNA-Seq transcriptomic BodyMap across 11 organs and 4 developmental stages
  • Description: 320 RNA samples isolated from 11 organs (adrenal gland, brain, heart, kidney, liver, lung, muscle, spleen, thymus, and testes or uterus) from both sexes of Fischer 344 rats across four developmental stages (2-, 6-, 21-, and 104-weeks-old)
  • BioProject: PRJNA238328
  • Publication: PMID 24510058
  • Analysis date: Mon Jun 6 17:44:12 2016

Pathways from PubChem

General gene information

Markers

Gene Ontology Provided by RGD

Function Evidence Code Pubs
enables magnesium ion binding IEA
Inferred from Electronic Annotation
more info
 
enables phosphoacetylglucosamine mutase activity IBA
Inferred from Biological aspect of Ancestor
more info
 
enables phosphoacetylglucosamine mutase activity ISO
Inferred from Sequence Orthology
more info
 
Process Evidence Code Pubs
involved_in UDP-N-acetylglucosamine biosynthetic process IBA
Inferred from Biological aspect of Ancestor
more info
 
involved_in UDP-N-acetylglucosamine biosynthetic process IEA
Inferred from Electronic Annotation
more info
 
acts_upstream_of_or_within UDP-N-acetylglucosamine biosynthetic process ISO
Inferred from Sequence Orthology
more info
 
involved_in UDP-N-acetylglucosamine biosynthetic process ISO
Inferred from Sequence Orthology
more info
 
involved_in biological_process ND
No biological Data available
more info
 
involved_in carbohydrate metabolic process IEA
Inferred from Electronic Annotation
more info
 
involved_in hemopoiesis IBA
Inferred from Biological aspect of Ancestor
more info
 
acts_upstream_of_or_within hemopoiesis ISO
Inferred from Sequence Orthology
more info
 
involved_in protein N-linked glycosylation ISO
Inferred from Sequence Orthology
more info
 
involved_in protein O-linked glycosylation ISO
Inferred from Sequence Orthology
more info
 
acts_upstream_of_or_within spermatogenesis ISO
Inferred from Sequence Orthology
more info
 

General protein information

Preferred Names
phosphoacetylglucosamine mutase
NP_001388122.1
XP_008764673.1
XP_063121858.1
XP_063121859.1

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001401193.1NP_001388122.1  phosphoacetylglucosamine mutase

    Status: VALIDATED

    Source sequence(s)
    JAXUCZ010000008
    UniProtKB/TrEMBL
    A0A9K3Y705, B2RYN0, D3ZFX4
    Related
    ENSRNOP00000062246.2, ENSRNOT00000067699.2

RefSeqs of Annotated Genomes: GCF_036323735.1-RS_2024_02

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCr8

Genomic

  1. NC_086026.1 Reference GRCr8

    Range
    96398331..96416045 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_063265788.1XP_063121858.1  phosphoacetylglucosamine mutase isoform X1

    UniProtKB/TrEMBL
    A6I1U8
  2. XM_063265789.1XP_063121859.1  phosphoacetylglucosamine mutase isoform X2

    UniProtKB/TrEMBL
    A0A9K3Y705, B2RYN0, D3ZFX4
  3. XM_008766451.4XP_008764673.1  phosphoacetylglucosamine mutase isoform X1

    See identical proteins and their annotated locations for XP_008764673.1

    UniProtKB/TrEMBL
    A6I1U8, A6I1U9
    Conserved Domains (2) summary
    cd03086
    Location:22525
    PGM3; PGM3 (phosphoglucomutase 3), also known as PAGM (phosphoacetylglucosamine mutase) and AGM1 (N-acetylglucosamine-phosphate mutase), is an essential enzyme found in eukaryotes that reversibly catalyzes the conversion of GlcNAc-6-phosphate into ...
    PLN02895
    Location:1523
    PLN02895; phosphoacetylglucosamine mutase

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001108772.1: Suppressed sequence

    Description
    NM_001108772.1: This RefSeq was removed because currently there is not sufficient data to support this transcript.