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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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INPP1
inositol polyphosphate-1-phosphatase
Chromosome 2 · 2q32.2
NCBI Gene: 3628Ensembl: ENSG00000151689.14HGNC: HGNC:6071UniProt: P49441
35PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindinginositol-1,4-bisphosphate 1-phosphatase activityinositol-1,3,4-trisphosphate 1-phosphatase activitysignal transductionupper extremity fractureneuroinflammatory disorderplacental retentioncleft palate
✦AI Summary

INPP1 (inositol polyphosphate-1-phosphatase) is an Mg2+-dependent phosphatase that catalyzes hydrolysis of the 1-position phosphate from inositol 1,4-bisphosphate and inositol 1,3,4-trisphosphate, key intermediates in phosphoinositide signaling 1. The gene is located on chromosome 2 and comprises six exons spanning >25 kb, with a 1.9 kb mRNA transcript expressed across all tissues, with notably higher levels in testis 2. INPP1 is significantly upregulated in human cancers. Transcription was upregulated in 42 of 49 colorectal tumors 1, and in cervical cancer, miR-27a-mediated INPP1 upregulation promotes cell viability, migration, invasion, and epithelial-mesenchymal transition 3. In osteosarcoma, INPP1 promotes cell migration and invasion through the TGF-β1/Smad2/3 pathway 4. Clinically, INPP1 has relevance to lithium-responsive bipolar disorder. INPP1 was postulated as a lithium target given its role in phospholipase C signaling 2. Genetic variability in INPP1 (rs909270, rs4853694, rs3791809) associates with lithium response and nonresponse in bipolar patients 5 and with suicidal behavior risk in bipolar populations 6. However, one study found INPP1 polymorphisms non-predictive of lithium response in type I bipolar disorder 7, and another identified INPP1 SNP rs2064721 interaction with post-traumatic stress disorder in lithium pharmacogenetics 8.

Sources cited
1
INPP1 catalyzes hydrolysis of inositol 1,3,4-trisphosphate and inositol 1,4-bisphosphate; transcription upregulated in 42/49 colorectal tumors
PMID: 10747296
2
INPP1 gene on chromosome 2q32 consists of six exons spanning >25 kb; 1.9 kb mRNA transcript in all tissues with highest expression in testis; INPP1 postulated as lithium target
PMID: 10780272
3
miR-27a upregulates INPP1 expression in cervical cancer; INPP1 overexpression promotes cell viability, migration, invasion, and EMT
PMID: 31557403
4
INPP1 promotes migration, proliferation, and invasion of osteosarcoma cells through TGF-β1/Smad2/3 pathway
PMID: 38047487
5
INPP1 rs909270-G polymorphism associates with lithium nonresponse in bipolar disorder; haplotype analysis shows association with lithium response
PMID: 26267417
6
INPP1 genetic variability (rs4853694, rs909270, rs3791809) associates with suicidal behavior risk in bipolar patients
PMID: 23453640
7
INPP1 C973A polymorphism not predictive of lithium prophylactic response in bipolar disorder type I patients
PMID: 16787706
8
INPP1 SNP rs2064721 interacts with post-traumatic stress disorder in lithium response pharmacogenetics
PMID: 17570738
Disease Associationsⓘ20
upper extremity fractureOpen Targets
0.28Weak
neuroinflammatory disorderOpen Targets
0.22Weak
placental retentionOpen Targets
0.19Weak
cleft palateOpen Targets
0.11Weak
retinopathyOpen Targets
0.11Weak
Fuchs endothelial corneal dystrophyOpen Targets
0.09Suggestive
early-onset non-syndromic cataractOpen Targets
0.08Suggestive
hypothyroidismOpen Targets
0.08Suggestive
Lisch epithelial corneal dystrophyOpen Targets
0.07Suggestive
X-linked endothelial corneal dystrophyOpen Targets
0.07Suggestive
X-linked corneal dermoidOpen Targets
0.07Suggestive
posterior polymorphous corneal dystrophyOpen Targets
0.07Suggestive
autosomal dominant keratitisOpen Targets
0.06Suggestive
congenital hereditary endothelial dystrophy of corneaOpen Targets
0.06Suggestive
lattice corneal dystrophy type IOpen Targets
0.06Suggestive
Central cloudy dystrophy of FrancoisOpen Targets
0.06Suggestive
central cloudy dystrophy of FrançoisOpen Targets
0.06Suggestive
Schnyder corneal dystrophyOpen Targets
0.06Suggestive
granular corneal dystrophy type IOpen Targets
0.06Suggestive
corneal dystrophy, punctiform and polychromatic pre-descemetOpen Targets
0.06Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
PLCG2Protein interaction96%IMPA2Protein interaction96%INPP5JProtein interaction94%INPP5AProtein interaction93%INPP4AProtein interaction93%BPNT2Protein interaction93%
Tissue Expression6 tissues
Brain
100%
Liver
99%
Bone Marrow
91%
Lung
89%
Heart
64%
Ovary
42%
Gene Interaction Network
Click a node to explore
INPP1PLCG2IMPA2INPP5JINPP5AINPP4ABPNT2
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt P49441
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
0.81LoF Tolerant
pLIⓘ
0.59Intermediate
Observed/Expected LoF0.31 [0.14–0.81]
RankingsWhere INPP1 stands among ~20K protein-coding genes
  • #10,988of 20,598
    Most Researched35
  • #6,853of 17,882
    Most Constrained (LOEUF)0.81
Genes detectedINPP1
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
INPP1 up-regulation by miR-27a contributes to the growth, migration and invasion of human cervical cancer.
PMID: 31557403
J Cell Mol Med · 2019
1.00
2
Genomic structure and sequence analysis of a human inositol polyphosphate 1-phosphatase gene (INPP1).
PMID: 10780272
Pharmacogenetics · 1999
0.90
3
Transcription of the inositol polyphosphate 1-phosphatase gene (INPP1) is upregulated in human colorectal cancer.
PMID: 10747296
Mol Carcinog · 2000
0.80
4
Retraction: INPP1 up-regulation by miR-27a contributes to the growth, migration and invasion of human cervical cancer.
PMID: 37485872
J Cell Mol Med · 2023
0.70
5
Association study of the INPP1, 5HTT, BDNF, AP-2beta and GSK-3beta GENE variants and restrospectively scored response to lithium prophylaxis in bipolar disorder.
PMID: 16787706
Neurosci Lett · 2006
0.60