HomeAboutRankingsData Sources
© 2026 GeneE
🧬
GeneE
10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
ⓘGeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
DAPP1
dual adaptor of phosphotyrosine and 3-phosphoinositides 1
Chromosome 4 · 4q23
NCBI Gene: 27071Ensembl: ENSG00000070190.13HGNC: HGNC:16500UniProt: J3KNB3
26PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingplasma membranephosphatidylinositol-3,4,5-trisphosphate bindingphosphatidylinositol-3,4-bisphosphate bindingAbnormality of the skeletal systemileostomyneuroinflammatory disorderulcerative colitis
✦AI Summary

DAPP1 (dual adaptor of phosphotyrosine and 3-phosphoinositides 1) is a 280 amino acid adapter protein containing an N-terminal myristoylation site, an SH2 domain, and a C-terminal pleckstrin homology (PH) domain 1. It binds with high affinity to phosphatidylinositol 3,4,5-trisphosphate and phosphatidylinositol 3,4-bisphosphate, serving as a molecular bridge between tyrosine-phosphorylated proteins and phosphoinositide signaling 1. DAPP1 functions as a B-cell-associated adapter regulating B-cell antigen receptor signaling downstream of PI3K 2. At the plasma membrane of activated lymphocytes, DAPP1 assembles protein complexes that promote activation of small GTPases including Rac and Rap, facilitating integrin activation and lymphocyte adhesion 2. DAPP1 is also recognized as a transcriptional target of T-bet in CD21lo B cell differentiation 3. Beyond lymphocyte function, DAPP1 acts as a negative regulator of platelet activation; DAPP1-deficient mice show enhanced thrombus formation and increased granule secretion 4. Genomic studies implicate DAPP1 variants in airway hyperreactivity responses to diesel exhaust particle exposure 5 and associate DAPP1 expression changes with treatment resistance in ulcerative colitis and systemic lupus erythematosus-like disease 67.

Sources cited
1
DAPP1 structural composition (SH2 and PH domains) and binding specificity to PtdIns(3,4,5)P3 and PtdIns(3,4)P2
PMID: 10432293
2
DAPP1 role in PI3K-regulated lymphocyte signaling, plasma membrane recruitment, and promotion of small GTPase activation
PMID: 19909369
3
DAPP1 as a T-bet-controlled lineage-defining gene in CD21lo B cell differentiation
PMID: 35867801
4
DAPP1 as a negative regulator of platelet function with enhanced thrombus formation in DAPP1-deficient mice
PMID: 29242851
5
DAPP1 role in gene-environment interaction for airway hyperreactivity to air pollution exposure
PMID: 31869344
6
DAPP1 as a key gene influencing ulcerative colitis treatment response and inflammatory progression
PMID: 38059894
7
DAPP1 association with autoimmune disease phenotypes in systemic lupus erythematosus-like disease
PMID: 26057447
Disease Associationsⓘ20
Abnormality of the skeletal systemOpen Targets
0.50Moderate
ileostomyOpen Targets
0.28Weak
neuroinflammatory disorderOpen Targets
0.10Weak
ulcerative colitisOpen Targets
0.08Suggestive
open-angle glaucomaOpen Targets
0.08Suggestive
infectionOpen Targets
0.07Suggestive
isolated agammaglobulinemiaOpen Targets
0.07Suggestive
Immunodeficiency due to a late component of complements deficiencyOpen Targets
0.07Suggestive
immune deficiency, familial variableOpen Targets
0.07Suggestive
hyper-IgM syndrome type 2Open Targets
0.07Suggestive
combined immunodeficiency with skin granulomasOpen Targets
0.07Suggestive
immunodeficiency, common variable, 4Open Targets
0.07Suggestive
immunodeficiency 86Open Targets
0.07Suggestive
hyper-IgM syndrome type 3Open Targets
0.07Suggestive
severe combined immunodeficiency due to CARD11 deficiencyOpen Targets
0.07Suggestive
agammaglobulinemia 8, autosomal dominantOpen Targets
0.06Suggestive
BENTA diseaseOpen Targets
0.06Suggestive
X-linked agammaglobulinemiaOpen Targets
0.06Suggestive
Autosomal recessive hyper-IgE syndromeOpen Targets
0.06Suggestive
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiencyOpen Targets
0.06Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
PTPN4Shared pathway100%CTDSP2Shared pathway100%PTPN18Shared pathway100%PPM1MShared pathway100%PTPN5Shared pathway100%CTDSP1Shared pathway100%
Tissue Expression6 tissues
Bone Marrow
100%
Lung
37%
Liver
5%
Heart
4%
Brain
3%
Ovary
2%
Gene Interaction Network
Click a node to explore
DAPP1PTPN4CTDSP2PTPN18PPM1MPTPN5CTDSP1
PROTEIN STRUCTURE
Preparing viewer…
PDB1FAO · 1.80 Å · X-ray
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
0.91LoF Tolerant
pLIⓘ
0.01Tolerant
Observed/Expected LoF0.57 [0.37–0.91]
RankingsWhere DAPP1 stands among ~20K protein-coding genes
  • #12,770of 20,598
    Most Researched26
  • #8,207of 17,882
    Most Constrained (LOEUF)0.91
Genes detectedDAPP1
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Human T-bet governs the generation of a distinct subset of CD11c
PMID: 35867801
Sci Immunol · 2022
1.00
2
DAPP1: a dual adaptor for phosphotyrosine and 3-phosphoinositides.
PMID: 10432293
Biochem J · 1999
0.90
3
Phosphoinositide 3-kinase-regulated adapters in lymphocyte activation.
PMID: 19909369
Immunol Rev · 2009
0.80
4
Comprehensive analysis reveals key genes and environmental toxin exposures underlying treatment response in ulcerative colitis based on
PMID: 38059894
Aging (Albany NY) · 2023
0.70
5
A GWAS approach identifies Dapp1 as a determinant of air pollution-induced airway hyperreactivity.
PMID: 31869344
PLoS Genet · 2019
0.60