HomeAboutRankingsData Sources
Β© 2026 GeneE
🧬
GeneE
3 sources retrieved Β· Most recent: April 2026 Β· Index updated 14 days ago
β“˜GeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
KRTAP13-3
keratin associated protein 13-3
Chromosome 21 Β· 21q22.11
NCBI Gene: 337960Ensembl: ENSG00000240432.4HGNC: HGNC:18925UniProt: Q3SY46
7PubMed Papers
3Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
βœ“ Experimental GO Evidenceβœ“ Swiss-Prot Reviewed
protein bindingcytosolneurodegenerative diseaseAbruptio Placentaeliver disease
✦AI Summary

KRTAP13-3 (keratin-associated protein 13-3) is a structural protein component of hair fibers located on chromosome 21. Primary function: KRTAP13-3 belongs to the high-glycine-tyrosine (HGT) class of keratin-associated proteins that form the interfilamentous matrix within hair cortex, embedding hair keratin intermediate filaments 1. Mechanism: These proteins are essential for hair shaft rigidity and resistance through extensive disulfide bond cross-linking with cysteine-rich hair keratins, creating a mechanically stable fiber structure. Disease relevance: KRTAP13-3 has been identified as a frequently mutated gene in atypical parathyroid tumors, appearing among the most commonly altered genes in whole-exome sequencing studies of these neoplasms 2. Clinical significance: KRTAP13-3 DNA methylation at specific CpG sites serves as a biomarker for cellular senescence in therapeutic cell products, enabling quality control assessment of mesenchymal stromal cells through epigenetic analysis during culture expansion 3. The gene's methylation status correlates with replicative senescence and can predict cumulative population doublings in cell preparations intended for clinical use.

Sources cited
1
KRTAP13-3 is a high-glycine-tyrosine keratin-associated protein component of hair fibers
PMID: 25279319
2
KRTAP13-3 is among the most frequently mutated genes identified in atypical parathyroid tumors
PMID: 38940486
3
KRTAP13-3 CpG site DNA methylation serves as a senescence biomarker for quality control of therapeutic cell preparations
PMID: 24755407
⚠Limited data available β€” This gene has 3 indexed publications. Summary and analysis may be incomplete.
Disease Associationsβ“˜3
neurodegenerative diseaseOpen Targets
0.30Weak
Abruptio PlacentaeOpen Targets
0.09Suggestive
liver diseaseOpen Targets
0.02Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar β†—
Related Genes
SCYGR1Protein interaction87%KRTAP24-1Protein interaction85%KRTAP26-1Protein interaction80%KRTAP20-2Protein interaction80%KRTAP6-3Protein interaction80%PRAMEF2Protein interaction77%
Tissue Expression6 tissues
Lung
0%
Ovary
0%
Bone Marrow
0%
Heart
0%
Liver
0%
Brain
0%
Gene Interaction Network
Click a node to explore
KRTAP13-3SCYGR1KRTAP24-1KRTAP26-1KRTAP20-2KRTAP6-3PRAMEF2
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted Β· UniProt Q3SY46
View on AlphaFold β†—
RankingsWhere KRTAP13-3 stands among ~20K protein-coding genes
  • #17,854of 20,598
    Most Researched7
Genes detectedKRTAP13-3
Sources retrieved3 papers
Response timeβ€”
πŸ“„ Sources
3
1
Proof of principle: quality control of therapeutic cell preparations using senescence-associated DNA-methylation changes.
PMID: 24755407
BMC Res Notes Β· 2014
1.00
2
The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans.
PMID: 25279319
Springerplus Β· 2014
0.67
3
Whole-exome Sequencing of Atypical Parathyroid Tumors Detects Novel and Common Genes Linked to Parathyroid Tumorigenesis.
PMID: 38940486
J Clin Endocrinol Metab Β· 2024
0.33