KLHL24 (kelch like family member 24)

2014-11-01  

Identity

HGNC
LOCATION
3q27.1
LOCUSID
ALIAS
DRE1,EBSSH,KRIP6
FUSION GENES

Other Information

Locus ID:

NCBI: 54800
MIM: 611295
HGNC: 25947
Ensembl: ENSG00000114796

Variants:

dbSNP: 54800
ClinVar: 54800
TCGA: ENSG00000114796
COSMIC: KLHL24

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000114796ENST00000242810Q6TFL4
ENSG00000114796ENST00000427201C9JMQ9
ENSG00000114796ENST00000437402C9JN72
ENSG00000114796ENST00000454495C9JCK3
ENSG00000114796ENST00000454652Q6TFL4
ENSG00000114796ENST00000468001C9J0A6
ENSG00000114796ENST00000468101C9JQ67
ENSG00000114796ENST00000473045C9JXR5
ENSG00000114796ENST00000476808Q6TFL4
ENSG00000114796ENST00000482138C9J3M5
ENSG00000114796ENST00000493074C9J2N4

Expression (GTEx)

0
5
10
15
20
25
30

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
277986262016Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility.13
186925132008The BTB/kelch protein, KRIP6, modulates the interaction of PICK1 with GluR6 kainate receptors.9
235122752013A microRNA encoded by HSV-1 inhibits a cellular transcriptional repressor of viral immediate early and early genes.9
278890622016Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin Fragility.8
285327582017The "Kelch" Surprise: KLHL24, a New Player in the Pathogenesis of Skin Fragility.5
297792542018Cardiomyopathy in patients with epidermolysis bullosa simplex with mutations in KLHL24.2
307153722019Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24.2
302265312019Phenotypic Features of Epidermolysis Bullosa Simplex due to KLHL24 Mutations in 3 Italian Cases.0

Citation

Dessen P

KLHL24 (kelch like family member 24)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/64968/klhl24