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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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GPRIN2
G protein regulated inducer of neurite outgrowth 2
Chromosome 10 · 10q11.22
NCBI Gene: 9721Ensembl: ENSG00000204175.7HGNC: HGNC:23730UniProt: O60269
17PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingneuron projection developmentplasma membraneneurodegenerative diseaselung adenocarcinomaneoplasmCOVID-19
✦AI Summary

GPRIN2 (G protein regulated inducer of neurite outgrowth 2) is a protein involved in neurite outgrowth and neuron projection development 1. The gene encodes a protein that binds to other cellular proteins and localizes to the plasma membrane [GO annotations from provided data]. Recent evidence from the T2T-CHM13 reference genome assembly confirms that GPRIN2 has multiple functional copies in the human genome, with proteomics data supporting its active expression 1. Mechanistically, GPRIN2 functions through a PI3K signaling pathway that regulates cellular proliferation and migration 2. In lung adenocarcinoma, GPRIN2 acts downstream of ferredoxin 1 (FDX1) to promote tumor cell proliferation, migration, and invasion; depletion of GPRIN2 reverses these pro-tumorigenic effects 2. Clinically, GPRIN2 variants are associated with multiple cancer types. Rare germline mutations in GPRIN2 are linked to familial esophageal squamous cell carcinoma risk 3, while somatic mutations appear in non-small-cell lung carcinoma across both adenocarcinoma and squamous cell carcinoma subtypes 4. GPRIN2 also functions as a mitophagy-related biomarker in psoriasis, where it correlates with disease severity and immune cell infiltration 5. Additionally, GPRIN2 variants are associated with breast cancer predisposition 6 and bipolar disorder genetic risk 7. These findings suggest GPRIN2 represents a pleiotropic gene with diverse roles in cancer development and neuropsychiatric disease.

Sources cited
1
GPRIN2 has functionally important gene copies confirmed by proteomics evidence in the T2T-CHM13 assembly
PMID: 38464973
2
GPRIN2 functions in PI3K signaling pathway promoting lung adenocarcinoma cell proliferation, migration, and invasion
PMID: 38802900
3
GPRIN2 carries rare damaging germline mutations associated with familial esophageal squamous cell carcinoma
PMID: 29405996
4
GPRIN2 somatic mutations detected in non-small-cell lung carcinoma patients across adenocarcinoma and squamous cell subtypes
PMID: 37694353
5
GPRIN2 identified as mitophagy-related biomarker for psoriasis diagnosis with correlation to immune cell infiltration
PMID: 40598168
6
GPRIN2 variants enriched in BRCA-negative breast cancer patients and associated with cancer susceptibility
PMID: 36424660
7
GPRIN2 copy number variant at 10q11.21 associated with bipolar disorder risk
PMID: 27244233
8
GPRIN2 identified as hub gene associated with abnormal coronary endothelial function in early atherosclerosis
PMID: 34800203
Disease Associationsⓘ20
neurodegenerative diseaseOpen Targets
0.28Weak
lung adenocarcinomaOpen Targets
0.04Suggestive
neoplasmOpen Targets
0.02Suggestive
COVID-19Open Targets
0.02Suggestive
Down syndromeOpen Targets
0.01Suggestive
colorectal cancerOpen Targets
0.01Suggestive
Intellectual disabilityOpen Targets
0.01Suggestive
myocardial infarctionOpen Targets
0.01Suggestive
hepatocellular carcinomaOpen Targets
0.00Suggestive
non-small cell lung carcinomaOpen Targets
0.00Suggestive
partial epilepsyOpen Targets
0.00Suggestive
psoriasisOpen Targets
0.00Suggestive
diabetes mellitusOpen Targets
0.00Suggestive
Alzheimer diseaseOpen Targets
0.00Suggestive
epilepsyOpen Targets
0.00Suggestive
esophageal squamous cell carcinomaOpen Targets
0.00Suggestive
colorectal carcinomaOpen Targets
0.00Suggestive
schizophreniaOpen Targets
0.00Suggestive
idiopathic pulmonary fibrosisOpen Targets
0.00Suggestive
ulcerative colitisOpen Targets
0.00Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
GPRIN3Shared pathway100%GPRIN1Shared pathway100%DRD5Protein interaction84%GTF2IProtein interaction84%UGT2B17Protein interaction84%NPEPPSProtein interaction84%
Tissue Expression6 tissues
Lung
100%
Liver
8%
Bone Marrow
4%
Ovary
1%
Brain
1%
Heart
0%
Gene Interaction Network
Click a node to explore
GPRIN2GPRIN3GPRIN1DRD5GTF2IUGT2B17NPEPPS
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt O60269
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.96LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF1.86 [0.91–1.96]
RankingsWhere GPRIN2 stands among ~20K protein-coding genes
  • #15,016of 20,598
    Most Researched17
  • #17,717of 17,882
    Most Constrained (LOEUF)1.96
Genes detectedGPRIN2
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Identification of molecular biomarkers associated with non-small-cell lung carcinoma (NSCLC) using whole-exome sequencing.
PMID: 37694353
Cancer Biomark · 2024
1.00
2
The T2T-CHM13 reference assembly uncovers essential WASH1 and GPRIN2 paralogues.
PMID: 38464973
Bioinform Adv · 2024
0.90
3
Identification of mitophagy-related biomarkers with immune cell infiltration in psoriasis.
PMID: 40598168
BMC Med Genomics · 2025
0.80
4
Familial Esophageal Squamous Cell Carcinoma with damaging rare/germline mutations in KCNJ12/KCNJ18 and GPRIN2 genes.
PMID: 29405996
Cancer Genet · 2018
0.70
5
Ferredoxin 1: a gatekeeper in halting lung adenocarcinoma progression through activation of the GPRIN2 signaling pathway.
PMID: 38802900
J Transl Med · 2024
0.60