Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3613
Gene name Gene Name - the full gene name approved by the HGNC.
Inositol monophosphatase 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
IMPA2
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
18
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
18p11.21
Summary Summary of gene provided in NCBI Entrez Gene.
This locus encodes an inositol monophosphatase. The encoded protein catalyzes the dephosphoylration of inositol monophosphate and plays an important role in phosphatidylinositol signaling. This locus may be associated with susceptibility to bipolar disord
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT042179 hsa-miR-484 CLASH 23622248
MIRT649264 hsa-miR-4797-5p HITS-CLIP 23824327
MIRT649263 hsa-miR-5007-5p HITS-CLIP 23824327
MIRT649261 hsa-miR-6748-3p HITS-CLIP 23824327
MIRT649262 hsa-miR-4421 HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183, 35271311
GO:0005737 Component Cytoplasm IDA 17068342
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol TAS
GO:0006020 Process Inositol metabolic process IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605922 6051 ENSG00000141401
Protein
UniProt ID O14732
Protein name Inositol monophosphatase 2 (IMP 2) (IMPase 2) (EC 3.1.3.25) (Inositol-1(or 4)-monophosphatase 2) (Myo-inositol monophosphatase A2)
Protein function Phosphatase that can use myo-inositol monophosphates, myo-inositol 1,4-diphosphate, scyllo-inositol-1,4-diphosphate, glucose-1-phosphate, beta-glycerophosphate and 2'-AMP as substrates in vitro (PubMed:17068342). It is likely that IMPA2 has an a
PDB 2CZH , 2CZI , 2CZK , 2DDK , 2FVZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00459 Inositol_P 16 282 Inositol monophosphatase family Family
Sequence
Sequence length 288
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Inositol phosphate metabolism
Metabolic pathways
Phosphatidylinositol signaling system
  Synthesis of IP2, IP, and Ins in the cytosol
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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
Diabetes Diabetic peripheral neuropathy in type 2 diabetes N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Bipolar Disorder Associate 20800640
Breast Neoplasms Stimulate 38048842
Calcinosis Cutis Associate 31202813
Carcinogenesis Associate 36740684
Carcinoma Ovarian Epithelial Associate 26889980
Carcinoma Renal Cell Associate 31202813
Cerebral Infarction Associate 27661109
Colorectal Neoplasms Associate 34743750
Leukemia Associate 19066393
Lymphoma Non Hodgkin Associate 26889980