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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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KRT35
keratin 35
Chromosome 17 · 17q21.2
NCBI Gene: 3886Ensembl: ENSG00000197079.9HGNC: HGNC:6453UniProt: Q92764
24PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
GO:0005615extracellular exosomeprotein bindingepithelial cell differentiationneurodegenerative diseaseGriscelli diseaseGriscelli syndrome type 3Griscelli disease type 3
✦AI Summary

KRT35 encodes keratin 35, a hair-specific intermediate filament protein that plays a crucial role in hair shaft structure and follicle development. KRT35 is expressed in specific zones of hair follicles during the anagen (growth) phase, with transcription occurring in a spatially organized pattern from the germinal matrix outward 1. The protein forms dimers with other keratins, such as KRT85, through hydrophobic interactions and hydrogen bonding, contributing to the structural integrity of hair fibers 2. KRT35 expression is regulated by transcription factors like HOXC13, and its downregulation occurs in Hoxc13 knockout models that exhibit hairless phenotypes 3. In disease contexts, KRT35 shows altered expression patterns in alopecia areata, with significant upregulation following corticosteroid treatment 4. The gene also demonstrates differentiation-specific expression in basal cell carcinomas, reflecting the tumor's hair follicle origin 5. Additionally, KRT35 exhibits accelerated evolution in hairless mammalian species, suggesting its importance in hair-related phenotypic variation across species 6. Beyond hair biology, KRT35 has forensic applications, as its RNA polymorphisms can be used for human identification from hair shaft samples 7.

Sources cited
1
KRT35 expression occurs in specific zones of hair follicles during anagen phase with spatially organized transcription pattern
PMID: 19272529
2
KRT35 forms dimers with KRT85 through hydrophobic interactions and hydrogen bonding
PMID: 26235519
3
KRT35 expression is regulated by HOXC13 and is downregulated in Hoxc13 knockout models
PMID: 28011715
4
KRT35 shows upregulation following corticosteroid treatment in alopecia areata
PMID: 26661294
5
KRT35 demonstrates differentiation-specific expression in basal cell carcinomas
PMID: 31580512
6
KRT35 shows accelerated evolution in hairless mammalian species
PMID: 36342464
7
KRT35 RNA polymorphisms can be used for human identification from hair shaft samples
PMID: 37611365
Disease Associationsⓘ20
neurodegenerative diseaseOpen Targets
0.29Weak
Griscelli diseaseOpen Targets
0.07Suggestive
Griscelli disease type 3Open Targets
0.06Suggestive
Griscelli syndrome type 3Open Targets
0.06Suggestive
oculocutaneous albinism type 3Open Targets
0.05Suggestive
Neurofibromatosis type 6Open Targets
0.05Suggestive
Griscelli disease type 1Open Targets
0.05Suggestive
Griscelli syndrome type 1Open Targets
0.05Suggestive
Tietz syndromeOpen Targets
0.05Suggestive
Tietze syndromeOpen Targets
0.05Suggestive
uncombable hair syndromeOpen Targets
0.04Suggestive
acroleukopathy, symmetricOpen Targets
0.04Suggestive
familial progressive hyperpigmentationOpen Targets
0.04Suggestive
hyperpigmentation with or without hypopigmentation, familial progressiveOpen Targets
0.04Suggestive
ermine phenotypeOpen Targets
0.04Suggestive
Microcephaly - albinism - digital anomaliesOpen Targets
0.04Suggestive
microcephaly-albinism-digital anomalies syndromeOpen Targets
0.04Suggestive
Waardenburg syndrome, IIa 2FOpen Targets
0.04Suggestive
prostate cancerOpen Targets
0.04Suggestive
Albinism-deafness syndromeOpen Targets
0.04Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
KRTAP3-1Protein interaction88%KRT25Protein interaction88%KRTAP4-7Protein interaction85%KRT71Protein interaction79%KRT85Protein interaction77%KRTAP11-1Protein interaction76%
Tissue Expression6 tissues
Lung
0%
Brain
0%
Heart
0%
Bone Marrow
0%
Liver
0%
Ovary
0%
Gene Interaction Network
Click a node to explore
KRT35KRTAP3-1KRT25KRTAP4-7KRT71KRT85KRTAP11-1
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt Q92764
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.00LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.76 [0.58–1.00]
RankingsWhere KRT35 stands among ~20K protein-coding genes
  • #13,222of 20,598
    Most Researched24
  • #9,699of 17,882
    Most Constrained (LOEUF)1.00
Genes detectedKRT35
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
A human identification system for hair shaft using RNA polymorphism.
PMID: 37611365
Forensic Sci Int Genet · 2023
1.00
2
Expression patterns of keratin intermediate filament and keratin associated protein genes in wool follicles.
PMID: 19272529
Differentiation · 2009
0.90
3
Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness.
PMID: 36342464
Elife · 2022
0.80
4
Generation of Hoxc13 knockout pigs recapitulates human ectodermal dysplasia-9.
PMID: 28011715
Hum Mol Genet · 2017
0.70
5
Biomarkers of alopecia areata disease activity and response to corticosteroid treatment.
PMID: 26661294
Exp Dermatol · 2016
0.60