PGM1 Gene

Name	phosphoglucomutase 1
Description	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 cells, PGM2 is a major isozyme. This gene is highly polymorphic. Mutations in this gene cause glycogen storage disease type 14. Alternativley spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Mar 2010]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nPhosphoglucomutase‐1 (PGM1) is a central metabolic enzyme that catalyzes the reversible interconversion of glucose 1‑phosphate and glucose 6‑phosphate. This reaction is pivotal for maintaining glucose homeostasis by balancing the flow of carbohydrates between glycolysis, gluconeogenesis, and glycogen synthesis. In doing so, PGM1 supplies the nucleotide sugars needed for proper protein N‑glycosylation and underpins cellular energy production and biosynthetic processes. Structural studies have revealed that precise ligand‐binding interactions and conformational dynamics in PGM1 are critical for its catalytic function, ensuring efficient substrate recognition and turnover."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its enzymatic core, PGM1 is tightly regulated by cellular signaling pathways that modulate its activity in response to metabolic needs and stress. For example, phosphorylation by the signaling kinase Pak1 and modulation via the AMPK–HDAC8 axis have been shown to enhance PGM1 activity, thereby integrating extracellular growth factor signals with intracellular energy status. In addition, extensive biochemical and crystallographic analyses of disease‑related missense and truncating variants demonstrate that subtle alterations—ranging from local disruptions in active‑site loops to extensive perturbations of interdomain interfaces—can result in catalytic impairment, misfolding, or instability. Such defects underlie the multisystem manifestations observed in PGM1 deficiency, a congenital disorder of glycosylation that can present with hypoglycemia, cardiomyopathy, hepatopathy, growth retardation, and even malignancy‐associated metabolic reprogramming. Moreover, studies in cancer models (e.g., hepatocellular carcinoma and glioma) indicate that dysregulated PGM1 expression contributes to altered glycogen metabolism and energy homeostasis, identifying PGM1 as a potential therapeutic target."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "5", "end_ref": "17"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Anupama Gururaj, Christopher J Barnes, Ratna K Vadlamudi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Regulation of phosphoglucomutase 1 phosphorylation and activity by a signaling kinase."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncogene (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.onc.1207969"}], "href": "https://doi.org/10.1038/sj.onc.1207969"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15378030"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15378030"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Eunju Bae, Hee Eun Kim, Eunjin Koh, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Phosphoglucomutase1 is necessary for sustained cell growth under repetitive glucose depletion."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS Lett (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.febslet.2014.06.034"}], "href": "https://doi.org/10.1016/j.febslet.2014.06.034"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24952355"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24952355"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Kyle M Stiers, Bailee N Kain, Abigail C Graham, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Induced Structural Disorder as a Molecular Mechanism for Enzyme Dysfunction in Phosphoglucomutase 1 Deficiency."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Mol Biol (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.jmb.2016.02.032"}], "href": "https://doi.org/10.1016/j.jmb.2016.02.032"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26972339"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26972339"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Paul Hoff Backe, Jon K Laerdahl, Lene Svendsen Kittelsen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Structural basis for substrate and product recognition in human phosphoglucomutase-1 (PGM1) isoform 2, a member of the α-D-phosphohexomutase superfamily."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41598-020-62548-0"}], "href": "https://doi.org/10.1038/s41598-020-62548-0"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32221390"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32221390"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Koichi Takahashi, Madoka Inuzuka, Tatsuya Ingi "}, {"type": "b", "children": [{"type": "t", "text": "Cellular signaling mediated by calphoglin-induced activation of IPP and PGM."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2004.10.021"}], "href": "https://doi.org/10.1016/j.bbrc.2004.10.021"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "15522220"}], "href": "https://pubmed.ncbi.nlm.nih.gov/15522220"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Yingying Lee, Kyle M Stiers, Bailee N Kain, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Compromised catalysis and potential folding defects in in vitro studies of missense mutants associated with hereditary phosphoglucomutase 1 deficiency."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Biol Chem (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1074/jbc.M114.597914"}], "href": "https://doi.org/10.1074/jbc.M114.597914"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25288802"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25288802"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Neta Loewenthal, Alon Haim, Ruti Parvari, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Phosphoglucomutase-1 deficiency: Intrafamilial clinical variability and common secondary adrenal insufficiency."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Med Genet A (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/ajmg.a.37294"}], "href": "https://doi.org/10.1002/ajmg.a.37294"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26768186"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26768186"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Kyle M Stiers, Abigail C Graham, Bailee N Kain, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Asp263 missense variants perturb the active site of human phosphoglucomutase 1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS J (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/febs.14025"}], "href": "https://doi.org/10.1111/febs.14025"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28117557"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28117557"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Yu Ding, Niu Li, Gouying Chang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Clinical and molecular genetic characterization of two patients with mutations in the phosphoglucomutase 1 (PGM1) gene."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Pediatr Endocrinol Metab (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1515/jpem-2017-0551"}], "href": "https://doi.org/10.1515/jpem-2017-0551"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29858906"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29858906"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Kyle M Stiers, Lesa J Beamer "}, {"type": "b", "children": [{"type": "t", "text": "A Hotspot for Disease-Associated Variants of Human PGM1 Is Associated with Impaired Ligand Binding and Loop Dynamics."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Structure (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.str.2018.07.005"}], "href": "https://doi.org/10.1016/j.str.2018.07.005"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30122451"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30122451"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Wo-Tu Tian, Xing-Hua Luan, Hai-Yan Zhou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neuromuscul Disord (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.nmd.2019.01.001"}], "href": "https://doi.org/10.1016/j.nmd.2019.01.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30737079"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30737079"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Kyle M Stiers, Reed P Hansen, Bana A Daghlas, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "AMPK-dependent phosphorylation of HDAC8 triggers PGM1 expression to promote lung cancer cell survival under glucose starvation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Lett (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.canlet.2020.03.007"}], "href": "https://doi.org/10.1016/j.canlet.2020.03.007"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32171858"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32171858"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Lesa J Beamer "}, {"type": "b", "children": [{"type": "t", "text": "Enzyme dysfunction at atomic resolution: Disease-associated variants of human phosphoglucomutase-1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochimie (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biochi.2020.08.017"}], "href": "https://doi.org/10.1016/j.biochi.2020.08.017"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32898648"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32898648"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Federica Conte, Eva Morava, Nurulamin Abu Bakar, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Genet Metab (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ymgme.2020.08.003"}], "href": "https://doi.org/10.1016/j.ymgme.2020.08.003"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33342467"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33342467"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Kyle M Stiers, Luckio F Owuocha, Lesa J Beamer "}, {"type": "b", "children": [{"type": "t", "text": "Effects of the T337M and G391V disease-related variants on human phosphoglucomutase 1: structural disruptions large and small."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Acta Crystallogr F Struct Biol Commun (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1107/S2053230X22004174"}], "href": "https://doi.org/10.1107/S2053230X22004174"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35506765"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35506765"}]}, {"type": "r", "ref": 17, "children": [{"type": "t", "text": "Shenghua Liu, Yuanyin Deng, Yunhu Yu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Knock-down of PGM1 inhibits cell viability, glycolysis, and oxidative phosphorylation in glioma under low glucose condition via the Myc signaling pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2023.03.034"}], "href": "https://doi.org/10.1016/j.bbrc.2023.03.034"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "36947965"}], "href": "https://pubmed.ncbi.nlm.nih.gov/36947965"}]}]}]}
Synonyms	CDG1T, GSD14
Proteins	PGM1_HUMAN
NCBI Gene ID	5236
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

PGM1 has 9,304 functional associations with biological entities spanning 9 categories (molecular profile, organism, disease, phenotype or trait, chemical, functional term, phrase or reference, structural feature, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 145 datasets.

Click the + buttons to view associations for PGM1 from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

PGM1 Gene

Functional Associations

Please acknowledge the Harmonizome in your publications by citing the following reference(s):

	Dataset	Summary
	Achilles Cell Line Gene Essentiality Profiles	cell lines with fitness changed by PGM1 gene knockdown relative to other cell lines from the Achilles Cell Line Gene Essentiality Profiles dataset.
	Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of PGM1 gene relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
	Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles	tissues with high or low expression of PGM1 gene relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
	Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles	tissue samples with high or low expression of PGM1 gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset.
	Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray	tissue samples with high or low expression of PGM1 gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
	Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq	tissue samples with high or low expression of PGM1 gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
	Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of PGM1 gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
	BioGPS Cell Line Gene Expression Profiles	cell lines with high or low expression of PGM1 gene relative to other cell lines from the BioGPS Cell Line Gene Expression Profiles dataset.
	BioGPS Human Cell Type and Tissue Gene Expression Profiles	cell types and tissues with high or low expression of PGM1 gene relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.
	BioGPS Mouse Cell Type and Tissue Gene Expression Profiles	cell types and tissues with high or low expression of PGM1 gene relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of PGM1 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.
	CCLE Cell Line Gene Expression Profiles	cell lines with high or low expression of PGM1 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CCLE Cell Line Proteomics	Cell lines associated with PGM1 protein from the CCLE Cell Line Proteomics dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with PGM1 gene from the CellMarker Gene-Cell Type Associations dataset.
	ChEA Transcription Factor Binding Site Profiles	transcription factor binding site profiles with transcription factor binding evidence at the promoter of PGM1 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of PGM1 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset.
	ChEA Transcription Factor Targets 2022	transcription factors binding the promoter of PGM1 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
	ClinVar Gene-Phenotype Associations	phenotypes associated with PGM1 gene from the curated ClinVar Gene-Phenotype Associations dataset.
	ClinVar Gene-Phenotype Associations 2025	phenotypes associated with PGM1 gene from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
	CMAP Signatures of Differentially Expressed Genes for Small Molecules	small molecule perturbations changing expression of PGM1 gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing PGM1 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing PGM1 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Experimental Protein Localization Evidence Scores	cellular components containing PGM1 protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.
	COMPARTMENTS Experimental Protein Localization Evidence Scores 2025	cellular components containing PGM1 protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores	cellular components co-occuring with PGM1 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025	cellular components co-occuring with PGM1 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	COSMIC Cell Line Gene CNV Profiles	cell lines with high or low copy number of PGM1 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with PGM1 gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Chemical Interactions	chemicals interacting with PGM1 gene/protein from the curated CTD Gene-Chemical Interactions dataset.
	CTD Gene-Disease Associations	diseases associated with PGM1 gene/protein from the curated CTD Gene-Disease Associations dataset.
	dbGAP Gene-Trait Associations	traits associated with PGM1 gene in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
	DeepCoverMOA Drug Mechanisms of Action	small molecule perturbations with high or low expression of PGM1 protein relative to other small molecule perturbations from the DeepCoverMOA Drug Mechanisms of Action dataset.
	DepMap CRISPR Gene Dependency	cell lines with fitness changed by PGM1 gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset.
	DISEASES Curated Gene-Disease Association Evidence Scores	diseases involving PGM1 gene from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Curated Gene-Disease Association Evidence Scores 2025	diseases involving PGM1 gene from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores	diseases associated with PGM1 gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores	diseases co-occuring with PGM1 gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores 2025	diseases co-occuring with PGM1 gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
	DisGeNET Gene-Disease Associations	diseases associated with PGM1 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with PGM1 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Phenoptype Associations dataset.