Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51292
Gene name Gene Name - the full gene name approved by the HGNC.
Guanosine monophosphate reductase 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
GMPR2
Synonyms (NCBI Gene) Gene synonyms aliases
GMPR 2, hGMPR-II
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q12
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes an enzyme that catalyzes the irreversible and NADPH-dependent reductive deamination of guanosine monophosphate (GMP) to inosine monophosphate (IMP). The protein also functions in the re-utilization of free intracellular bases and purine
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022133 hsa-miR-124-3p Microarray 18668037
MIRT027420 hsa-miR-98-5p Microarray 19088304
MIRT041522 hsa-miR-193b-3p CLASH 23622248
MIRT1022761 hsa-let-7a CLIP-seq
MIRT1022762 hsa-let-7b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003824 Function Catalytic activity IEA
GO:0003920 Function GMP reductase activity IDA 12669231, 22037469
GO:0003920 Function GMP reductase activity IEA
GO:0005515 Function Protein binding IPI 25416956, 33961781
GO:0005829 Component Cytosol TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610781 4377 ENSG00000100938
Protein
UniProt ID Q9P2T1
Protein name GMP reductase 2 (GMPR 2) (EC 1.7.1.7) (Guanosine 5'-monophosphate oxidoreductase 2) (Guanosine monophosphate reductase 2)
Protein function Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides
PDB 2A7R , 2BZN , 2C6Q
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00478 IMPDH 9 341 IMP dehydrogenase / GMP reductase domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in heart, skeletal muscle, kidney, brain, liver, prostate, spleen, placenta, testis and ovary. Low expression in colon, thymus and peripheral blood leukocytes. {ECO:0000269|PubMed:12009299, ECO:0000269|PubMed:12669231}
Sequence
Sequence length 348
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Purine metabolism
Metabolic pathways
Nucleotide metabolism
  Purine salvage
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Uterine Fibroids Uterine fibroids N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Neoplasms Associate 12669231