KLHL24 Chromosome 3
Kelch like family member 24
Upload your DNA to see your personal genotypes for variants in KLHL24.
What This Gene Does
The protein encoded by this gene is a ubiquitin ligase substrate receptor and is regulated by autoubiquitination. Variations in the translation initiation codon of this gene have been found, which result in an N-terminally truncated but more stable protein due to loss of the autoubiquitination function. The more stable mutant protein causes an increased ubiquitin and degradation of keratin 14, which leads to skin fragility and the potentially life-threatening disease epidermolysis bullosa. The encoded protein is also involved in the regulation of kainate receptors. [provided by RefSeq, Mar 2017]
Gene Info
Gene Group
"Kelch like|BTB domain containing"
Locus Type
gene with protein product
Location
3q27.1
Ensembl
ENSG00000114796
Associated Conditions (11)
Inborn genetic diseases
KLHL24-related disorder
Cardiomyopathy
Epidermolysis bullosa simplex
Koebner type
Epidermolysis bullosa simplex 6
generalized
with scarring and hair loss
familial hypertrophic
29
with polyglucosan bodies
Key Variants
RS117473658
Conflicting classifications of pathogenicity
Inborn genetic diseases, KLHL24-related disorder, Inborn genetic diseases
Health Risk
RS138664031
Conflicting classifications of pathogenicity
Inborn genetic diseases, Cardiomyopathy, Inborn genetic diseases
Health Risk
RS762218625
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1057515580
Pathogenic
Epidermolysis bullosa simplex, Koebner type, Epidermolysis bullosa simplex 6
Health Risk
RS2545651806
Pathogenic
Cardiomyopathy, familial hypertrophic, 29
Health Risk
RS778943927
Pathogenic
Cardiomyopathy, familial hypertrophic, 29
Health Risk
RS886037956
Pathogenic
Epidermolysis bullosa simplex, Koebner type, Epidermolysis bullosa simplex 6
Health Risk
RS886037957
Pathogenic
Epidermolysis bullosa simplex, Koebner type, Epidermolysis bullosa simplex 6
Health Risk
All Variants (8)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS117473658 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, KLHL24-related disorder, Inborn genetic diseases |
| RS138664031 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Cardiomyopathy, Inborn genetic diseases |
| RS762218625 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS1057515580 | Health Risk | Pathogenic | Epidermolysis bullosa simplex, Koebner type, Epidermolysis bullosa simplex 6 |
| RS2545651806 | Health Risk | Pathogenic | Cardiomyopathy, familial hypertrophic, 29 |
| RS778943927 | Health Risk | Pathogenic | Cardiomyopathy, familial hypertrophic, 29 |
| RS886037956 | Health Risk | Pathogenic | Epidermolysis bullosa simplex, Koebner type, Epidermolysis bullosa simplex 6 |
| RS886037957 | Health Risk | Pathogenic | Epidermolysis bullosa simplex, Koebner type, Epidermolysis bullosa simplex 6 |