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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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ATRN
attractin
Chromosome 20 · 20p13
NCBI Gene: 8455Ensembl: ENSG00000088812.19HGNC: HGNC:885UniProt: B4DZ36
51PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
FUNCTIONAL ROLE
Receptor
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
GO:0005615extracellular exosomesignaling receptor activityplasma membraneAbnormality of the skeletal systemneurodegenerative diseaselung carcinomaosteitis deformans
✦AI Summary

ATRN (attractin) is a multifunctional cell adhesion protein encoded on chromosome 20 that exists as both secreted and transmembrane isoforms generated through alternative splicing 1. The gene produces a soluble form with dipeptidyl peptidase IV activity released by activated T lymphocytes and a membrane-bound form that regulates cell-cell interactions during inflammatory responses 1. ATRN plays a critical role in central nervous system myelination; loss-of-function mutations cause age-dependent neurodegeneration with hypomyelination, neuronal cell death, and vacuolation 23. The protein exhibits neuroprotective functions by regulating mitochondrial homeostasis and preventing cytochrome c release and apoptosis-inducing factor release in response to neurotoxins 2. ATRN mutations impair working memory through reduced myelin basic protein expression 4. Clinically, elevated serum ATRN levels have been identified as a potential biomarker in inflammatory bowel disease patients compared to healthy controls 5, and ATRN was identified as an early serum marker for preeclampsia risk prediction, contributing to complement, coagulation, and growth factor signaling pathways 6. These findings establish ATRN as a key regulator of neurological development and immune homeostasis with disease relevance across neurodevelopmental and inflammatory conditions.

Sources cited
1
ATRN produces both secreted and membrane-bound isoforms through alternative splicing; soluble form is released by activated T lymphocytes with dipeptidyl peptidase IV activity
PMID: 10811918
2
ATRN loss-of-function causes age-dependent neurodegeneration; ATRN protects against neurotoxin-induced neuronal death by regulating mitochondrial function and preventing cytochrome c/AIF release
PMID: 16860906
3
Homozygous ATRN mutations cause hypomyelinating leukodystrophy with impaired CNS myelination, developmental delay, and spasticity
PMID: 28493104
4
ATRN mutations impair working memory in rats through reduced myelin basic protein expression
PMID: 36621889
5
Elevated serum ATRN levels identified as biomarker in inflammatory bowel disease patients compared to healthy controls
PMID: 41063386
6
ATRN identified as early serum marker for preeclampsia risk prediction in first trimester; participates in complement, coagulation, and growth factor pathways
PMID: 39408980
Disease Associationsⓘ20
Abnormality of the skeletal systemOpen Targets
0.45Moderate
neurodegenerative diseaseOpen Targets
0.37Weak
lung carcinomaOpen Targets
0.25Weak
osteitis deformansOpen Targets
0.24Weak
autismOpen Targets
0.12Weak
Global developmental delayOpen Targets
0.12Weak
ThrombocytopeniaOpen Targets
0.12Weak
Griscelli diseaseOpen Targets
0.09Suggestive
Griscelli disease type 3Open Targets
0.09Suggestive
Griscelli syndrome type 3Open Targets
0.09Suggestive
uncombable hair syndromeOpen Targets
0.08Suggestive
Microcephaly - albinism - digital anomaliesOpen Targets
0.07Suggestive
microcephaly-albinism-digital anomalies syndromeOpen Targets
0.07Suggestive
Griscelli disease type 1Open Targets
0.07Suggestive
Griscelli syndrome type 1Open Targets
0.07Suggestive
oculocutaneous albinism type 3Open Targets
0.06Suggestive
Spinocerebellar ataxia type 40Open Targets
0.06Suggestive
Tietz syndromeOpen Targets
0.06Suggestive
Tietze syndromeOpen Targets
0.06Suggestive
Young adult-onset ParkinsonismOpen Targets
0.06Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
MC1RProtein interaction99%MGRN1Protein interaction99%MC4RProtein interaction87%ASIPProtein interaction83%ANKRD46Protein interaction78%RNF157Protein interaction77%
Tissue Expression6 tissues
Liver
100%
Brain
94%
Heart
89%
Ovary
43%
Bone Marrow
37%
Lung
36%
Gene Interaction Network
Click a node to explore
ATRNMC1RMGRN1MC4RASIPANKRD46RNF157
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt O75882
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
0.40Moderately Constrained
pLIⓘ
1.00Intolerant
Observed/Expected LoF0.31 [0.24–0.40]
RankingsWhere ATRN stands among ~20K protein-coding genes
  • #8,646of 20,598
    Most Researched51
  • #1,955of 17,882
    Most Constrained (LOEUF)0.40 · top quartile
Genes detectedATRN
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Polycystic ovary syndrome.
PMID: 35934017
Lancet Diabetes Endocrinol · 2022
1.00
2
Secreted and membrane attractin result from alternative splicing of the human ATRN gene.
PMID: 10811918
Proc Natl Acad Sci U S A · 2000
0.90
3
[Attractin].
PMID: 16251053
Zhonghua Bing Li Xue Za Zhi · 2005
0.80
4
Comprehensive proteomic profile in newly diagnosed patients with inflammatory bowel disease: identification of potential biomarkers.
PMID: 41063386
J Crohns Colitis · 2025
0.70
5
Mutation of the attractin gene impairs working memory in rats.
PMID: 36621889
Brain Behav · 2023
0.60