IMPA1 - inositol monophosphatase 1 Gene

Also Known as IMP; IMPA; MRT59

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 3612

About IMPA1

Cytogenetic location: 8q21.13 Genomic coordinates (GRCh38): 8:81,656,914-81,686,325 (from NCBI)

This gene has 13 transcripts (splice variants), 232 orthologues, 4 paralogues and is associated with 1 phenotype. Ubiquitous expression in testis (RPKM 15.5), thyroid (RPKM 10.4) and 24 other tissues.

Summary

This gene encodes an enzyme that dephosphorylates myo-inositol monophosphate to generate free myo-inositol, a precursor of phosphatidylinositol, and is therefore an important modulator of intracellular signal transduction via the production of the second messengers myoinositol 1,4,5-trisphosphate and diacylglycerol. This enzyme can also use myo-inositol-1,3-diphosphate, myo-inositol-1,4-diphosphate, scyllo-inositol-phosphate, glucose-1-phosphate, glucose-6-phosphate, fructose-1-phosphate, beta-glycerophosphate, and 2'-AMP as substrates. This enzyme shows magnesium-dependent Phosphatase activity and is inhibited by therapeutic concentrations of lithium. Inhibition of inositol monophosphate hydroylosis and subsequent depletion of inositol for phosphatidylinositol synthesis may explain the anti-manic and anti-depressive effects of lithium administered to treat bipolar disorder. Alternative splicing results in multiple transcript variants encoding distinct isoforms. A pseudogene of this gene is also present on chromosome 8q21.13. [provided by RefSeq, Dec 2014]

IMPA1 Products (3)

mRNA Protein Name
NM_001144878.2 NP_001138350.1 inositol monophosphatase 1 isoform 2
NM_001144879.2 NP_001138351.1 inositol monophosphatase 1 isoform 3
NM_005536.4 NP_005527.1 inositol monophosphatase 1 isoform 1
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables inositol monophosphate 1-phosphatase activity IDA
IDA: Inferred from direct assay
17068342 GOA
enables inositol monophosphate 1-phosphatase activity IMP
IMP: Inferred from mutant phenotype
1377913 GOA
enables inositol monophosphate phosphatase activity IDA
IDA: Inferred from direct assay
9462881 GOA
enables lithium ion binding IDA
IDA: Inferred from direct assay
9462881 GOA
enables magnesium ion binding IDA
IDA: Inferred from direct assay
9462881 GOA
enables manganese ion binding IDA
IDA: Inferred from direct assay
9462881 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables protein homodimerization activity IDA
IDA: Inferred from direct assay
17068342 GOA
Biological Process GO Annotation Evidence References Source
involved in phosphate-containing compound metabolic process IMP
IMP: Inferred from mutant phenotype
1377913 GOA
involved in phosphatidylinositol biosynthetic process IMP
IMP: Inferred from mutant phenotype
1377913 GOA
involved in signal transduction IMP
IMP: Inferred from mutant phenotype
1377913 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
1377913 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

IMPA1 Protein Structure

Inositol_P

Inositol_P: Inositol monophosphatase family (7 - 267)

  • 0
  • 100
  • 200
  • 277 a.a.
Protein Preferred Names Protein Names

inositol monophosphatase 1

  • D-galactose 1-phosphate phosphatase

IMPA1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
IMPA1 P29218 IMPA2 Homo sapiens O14732 35271311
Intra
IMPA1 P29218 IMPA2 Homo sapiens O14732 25416956
Intra
IMPA1 P29218 IMPA1 Homo sapiens P29218-1 31515488
Intra
IMPA1 P29218 IMPA1 Homo sapiens P29218 16189514
Intra
IMPA1 P29218 IMPA1 Homo sapiens P29218 19447967
Intra
IMPA1 P29218 SIRT1 Homo sapiens Q96EB6 33961781
Intra
IMPA1 P29218 IMPA1 Homo sapiens P29218 25416956
Intra
IMPA1 P29218 METTL18 Homo sapiens O95568 33961781
Intra
IMPA1 P29218 E6 Human papillomavirus 5 P06930 22810586
Intra
IMPA1 P29218 IMPA1 Homo sapiens P29218
Y2H
21516116
Intra
IMPA1 P29218 Impa1 Rattus norvegicus P97697 8068621
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant IMPA1 Proteins

Cat. No. Product Name Accession Purity
HY-P70335 IMPA1 Protein, Human (His) P29218-1 (M1-D277) ≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Intellectual Developmental Disorder, Autosomal Recessive 59
  • MRT59

  • Mental Retardation, Autosomal Recessive 59

  • Autosomal Recessive Intellectual Developmental Disorder 59

Bipolar Disorder
  • Bipolar Depression

  • Manic Disorder

  • Depression, Bipolar

  • Bipolar Disorder Manic Phase

  • Depressive-Manic Psych.

  • Manic Bipolar Affective Disorder

  • Manic Bipolar I Disorder

  • Manic Depression

  • Manic Depressive Disorder

  • Mixed Bipolar Disorder

  • Bipolar Affective Disorder

  • Bipolar Affective Psychosis

  • Bipolar Spectrum Disorder

  • Manic Depressive Illness

  • Depression Bipolar

  • Bipolar Disorder, Mixed

  • Major Affective Disorder

  • Major Affective Disorder 1

  • Major Affective Disorder 2

Mood Disorder
  • Mood Disorders

  • Episodic Mood Disorder

Spastic Paraplegia, Optic Atrophy, And Neuropathy
  • Spoan Syndrome

  • SPOAN

  • Spastic Paraplegia, Optic Atropy, And Neuropathy

  • Spastic Paraplegia, Optic Atropy, And Neuropathy Syndrome

  • Spastic Paraplegia-Optic Atrophy-Neuropathy Syndrome

Developmental And Epileptic Encephalopathy 11
  • Epileptic Encephalopathy, Early Infantile, 11

  • DEE11

  • Eiee11

  • Developmental And Epileptic Encephalopathy, 11

  • Early Infantile Epileptic Encephalopathy 11

  • Encephalopathy, Developmental And Epileptic, Type 11

Cardiomyopathy, Familial Hypertrophic, 1
  • Asymmetric Septal Hypertrophy

  • Familial Hypertrophic Cardiomyopathy

  • Hypertrophic Cardiomyopathy 1

  • CMH1

  • Hypertrophic Cardiomyopathy 19

  • CMH

  • Ventricular Hypertrophy, Hereditary

  • Ash

  • Hypertrophic Subaortic Stenosis, Idiopathic

  • Cardiomyopathy, Familial Hypertrophic

  • Cardiomyopathy, Hypertrophic, 1, Digenic

  • Cardiomyopathy, Familial Hypertrophic 1

  • Hcm

  • Hereditary Ventricular Hypertrophy

  • Idiopathic Hypertrophic Subaortic Stenosis

  • Hypertrophic Cardiomyopathy

  • Cardiomyopathy, Hypertrophic, Familial

  • Cardiomyopathy, Hypertrophic, 1

  • Familial Asymmetric Septal Hypertrophy

  • Heritable Hypertrophic Cardiomyopathy

  • Fhc

  • Cardiomyopathy, Hypertrophic, Familial, Type 1

Schizophrenia
  • SCZD

  • Schizophrenia With Or Without An Affective Disorder

  • Schizophrenia 12

  • Schizophrenia, Susceptibility To

  • Schizophrenia-1

  • Dementia Praecox

  • Schizophrenia 1

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris IMPA1 VGNC VGNC:42007
Bos taurus IMPA1 VGNC VGNC:30184
Mus musculus IMPA1 MGD MGI:1933158
Macaca mulatta IMPA1 VGNC VGNC:84008
Rattus norvegicus IMPA1 RGD RGD:69254
Felis catus IMPA1 VGNC VGNC:67796
Others IMPA1 NCBI