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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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KRT77
keratin 77
Chromosome 12 · 12q13.13
NCBI Gene: 374454Ensembl: ENSG00000189182.10HGNC: HGNC:20411UniProt: Q0IIN1
60PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingcytoskeletonextracellular exosomeintermediate filament organizationbenign chondrogenic neoplasmProptosisenteritisovarian dysfunction
✦AI Summary

KRT77 (keratin 77) encodes a type II epithelial keratin that plays important roles in epidermal development and environmental adaptation. KRT77 is expressed in human and mouse sweat gland ducts and shows coordinated expression with other epidermal differentiation markers during skin morphogenesis 12. The gene is located within the type II keratin gene cluster on chromosome 12.13 and represents one of seven novel type II keratins identified in hair follicle/epidermal appendages 34. Functionally, KRT77 contributes to keratinocyte structural integrity, with compensation mechanisms evident when absent - KRT77-deficient mice show upregulated KRT1 expression, suggesting functional redundancy among type II keratins 1. The gene exhibits environmental adaptation significance, with insertion variants correlating with climate parameters in cattle populations 5. KRT77 appears in disease contexts, being upregulated in viral myocarditis plasma exosomes 6 and decreasing during COVID-19 recovery 7. In psoriasis, KRT77 upregulation is associated with normalized keratinocyte function through inhibition of Notch signaling 8. These findings indicate KRT77's dual roles in normal epidermal homeostasis and pathological responses.

Sources cited
1
KRT77 expression in sweat gland ducts and functional compensation by KRT1 when absent
PMID: 39603462
2
Coordinated expression during epidermal morphogenesis with other differentiation markers
PMID: 17330888
3
Location in chromosome 12q13.13 keratin gene cluster
PMID: 15737194
4
Identification as one of seven novel type II keratins in hair follicle/epidermal appendages
PMID: 11683385
5
Environmental adaptation significance with climate-correlated insertion variants in cattle
PMID: 37452660
6
Upregulation in viral myocarditis plasma exosomes
PMID: 30772974
7
Decreased levels during COVID-19 recovery
PMID: 40341493
8
Role in psoriasis treatment through Notch signaling inhibition and keratinocyte function normalization
PMID: 41348204
Disease Associationsⓘ20
benign chondrogenic neoplasmOpen Targets
0.18Weak
ProptosisOpen Targets
0.17Weak
enteritisOpen Targets
0.15Weak
ovarian dysfunctionOpen Targets
0.05Suggestive
rectosigmoid junction neoplasmOpen Targets
0.05Suggestive
hypoparathyroidism, familial isolated, 2Open Targets
0.04Suggestive
psoriasisOpen Targets
0.04Suggestive
isolated hyperchlorhidrosisOpen Targets
0.04Suggestive
Hearing loss - familial salivary gland insensitivity to aldosteroneOpen Targets
0.03Suggestive
hearing loss-familial salivary gland insensitivity to aldosterone syndromeOpen Targets
0.03Suggestive
familial isolated hyperparathyroidismOpen Targets
0.03Suggestive
hyperparathyroidismOpen Targets
0.03Suggestive
Crohn's diseaseOpen Targets
0.03Suggestive
DNA methylationOpen Targets
0.03Suggestive
rosaceaOpen Targets
0.02Suggestive
inherited hemoglobinopathyOpen Targets
0.02Suggestive
neoplasmOpen Targets
0.02Suggestive
Mantle cell lymphomaOpen Targets
0.01Suggestive
microphthalmia with limb anomaliesOpen Targets
0.01Suggestive
goutOpen Targets
0.01Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
KRT7Shared pathway100%KRT81Shared pathway100%KRT82Shared pathway100%KRT86Shared pathway100%KRT75Shared pathway100%KRT72Shared pathway100%
Tissue Expression6 tissues
Bone Marrow
100%
Liver
56%
Lung
33%
Ovary
33%
Brain
0%
Heart
0%
Gene Interaction Network
Click a node to explore
KRT77KRT7KRT81KRT82KRT86KRT75KRT72
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt Q0IIN1
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
1.11LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.85 [0.66–1.11]
RankingsWhere KRT77 stands among ~20K protein-coding genes
  • #7,680of 20,598
    Most Researched60
  • #11,375of 17,882
    Most Constrained (LOEUF)1.11
Genes detectedKRT77
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
The loss of keratin 77 in murine skin is functionally compensated by keratin 1.
PMID: 39603462
Biochim Biophys Acta Mol Cell Res · 2025
1.00
2
The genetic secrets of adaptation: decoding the significance of the 30-bp insertion in the
PMID: 37452660
Anim Biotechnol · 2023
0.90
3
[Biomarkers screening for viral myocarditis through proteomics analysis of plasma exosomes].
PMID: 30772974
Zhonghua Yi Xue Za Zhi · 2019
0.80
4
Exhaled breath protein composition in patients hospitalised during the first wave of COVID-19.
PMID: 40341493
J Breath Res · 2025
0.70
5
Characterization of new members of the human type II keratin gene family and a general evaluation of the keratin gene domain on chromosome 12q13.13.
PMID: 15737194
J Invest Dermatol · 2005
0.60