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GeneE
7 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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NCMAP
non-compact myelin associated protein
Chromosome 1 · 1p36.11
NCBI Gene: 400746Ensembl: ENSG00000184454.8HGNC: HGNC:29332UniProt: Q5T1S8
5PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
structural constituent of myelin sheathSchmidt-Lanterman incisureplasma membranepositive regulation of myelinationuterine polypinherited retinal dystrophyCOVID-19severe acute respiratory syndrome
✦AI Summary

NCMAP (non-compact myelin associated protein) is a structural component of peripheral nervous system myelin with roles in myelin formation and maintenance. Based on GO annotations and sequence localization data, NCMAP localizes to paranodal regions and Schmidt-Lanterman incisures of myelinated axons, suggesting involvement in myelin organization at these specialized structures. The gene positively regulates myelination processes in the peripheral nervous system. At the molecular level, NCMAP functions as a structural constituent of the myelin sheath, likely contributing to the mechanical integrity and organization of non-compact myelin domains. Its precise biochemical mechanism remains to be fully characterized, though its localization pattern suggests roles in axonal insulation and myelin stability. Clinical relevance of NCMAP is emerging in two contexts. First, altered NCMAP expression has been identified in pre-eclamptic placentae, where it was among 53 differentially expressed genes associated with disturbed vascular function 1. Second, a genetic variant NCMAP rs4553122 was identified as significantly associated with peak anti-Factor Xa levels in patients receiving rivaroxaban anticoagulation therapy for nonvalvular atrial fibrillation, suggesting potential involvement in pharmacodynamic variation 2. These findings indicate NCMAP may have broader physiological functions beyond myelin structure, though additional investigation is needed to establish causal relationships and clinical significance.

Sources cited
1
NCMAP was identified as a differentially expressed gene in pre-eclamptic placentae, among genes potentially involved in pathogenesis or biomarkers for this pregnancy complication
PMID: 26388242
2
NCMAP rs4553122 SNP was significantly associated with peak anti-FXa level in patients receiving rivaroxaban for nonvalvular atrial fibrillation
PMID: 37203300
⚠Limited data available — This gene has 2 indexed publications. Summary and analysis may be incomplete.
Disease Associationsⓘ20
uterine polypOpen Targets
0.33Weak
inherited retinal dystrophyOpen Targets
0.27Weak
COVID-19Open Targets
0.25Weak
severe acute respiratory syndromeOpen Targets
0.25Weak
Barrett's esophagusOpen Targets
0.05Suggestive
esophageal adenocarcinomaOpen Targets
0.04Suggestive
breast carcinomaOpen Targets
0.04Suggestive
Peptic ulcerOpen Targets
0.03Suggestive
hair colorOpen Targets
0.03Suggestive
Abruptio PlacentaeOpen Targets
0.03Suggestive
chronic fatigue syndromeOpen Targets
0.02Suggestive
hypothyroidismOpen Targets
0.02Suggestive
schizophreniaOpen Targets
0.02Suggestive
Down syndromeOpen Targets
0.02Suggestive
placental retentionOpen Targets
0.02Suggestive
autoimmune thyroid diseaseOpen Targets
0.02Suggestive
obesityOpen Targets
0.02Suggestive
gastric carcinomaOpen Targets
0.01Suggestive
acute myeloid leukemiaOpen Targets
0.01Suggestive
Tetralogy of FallotOpen Targets
0.01Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
CDK18Shared pathway33%ZNF488Shared pathway33%NKX6-2Shared pathway33%TENM4Shared pathway25%LGI4Shared pathway25%CST7Shared pathway20%
Tissue Expression6 tissues
Liver
100%
Lung
44%
Bone Marrow
14%
Brain
14%
Heart
7%
Ovary
4%
Gene Interaction Network
Click a node to explore
NCMAPCDK18ZNF488NKX6-2TENM4LGI4CST7
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q5T1S8
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.89LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF1.34 [0.81–1.89]
RankingsWhere NCMAP stands among ~20K protein-coding genes
  • #18,373of 20,598
    Most Researched5
  • #17,240of 17,882
    Most Constrained (LOEUF)1.89
Genes detectedNCMAP
Sources retrieved7 papers
Response time—
📄 Sources
7▼
1
The Immunopeptidome from a Genomic Perspective: Establishing the Noncanonical Landscape of MHC Class I-Associated Peptides.
PMID: 36961404
Cancer Immunol Res · 2023
1.00
2
Gene expression profiling of pre-eclamptic placentae by RNA sequencing.
PMID: 26388242
Sci Rep · 2015
0.86
3
Genetic variants influenced the risk of bleeding and pharmacodynamics of rivaroxaban in patients with nonvalvular atrial fibrillation: A multicentre prospective cohort study.
PMID: 37203300
Clin Transl Med · 2023
0.71
4
pXg: Comprehensive Identification of Noncanonical MHC-I-Associated Peptides From De Novo Peptide Sequencing Using RNA-Seq Reads.
PMID: 38403075
Mol Cell Proteomics · 2024
0.57
5
Mutation spectrum and differential gene expression in cystic and solid vestibular schwannoma.
PMID: 24030433
Genet Med · 2014
0.43