2. Gene
  3. KLHL24 - kelch like family member 24 Gene

KLHL24 - kelch like family member 24 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as DRE1; EBS6; EBSSH; KRIP6

Gene ID: 54800 | Gene type: protein coding

About KLHL24

Cytogenetic location: 3q27.1 Genomic coordinates (GRCh38): 3:183,635,623-183,684,519 (from NCBI)

This gene has 15 transcripts (splice variants), 223 orthologues, 54 paralogues and is associated with 2 phenotypes. Ubiquitous expression in heart (RPKM 9.5), thyroid (RPKM 9.3) and 25 other tissues.

Summary

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]

KLHL24 Products(17)

mRNA Protein Name
NM_001349413.1 NP_001336342.1 kelch-like protein 24 isoform a
NM_001349414.1 NP_001336343.1 kelch-like protein 24 isoform a
NM_001349415.1 NP_001336344.1 kelch-like protein 24 isoform a
NM_001349416.1 NP_001336345.1 kelch-like protein 24 isoform a
NM_001349417.1 NP_001336346.1 kelch-like protein 24 isoform a
NM_001349418.1 NP_001336347.1 kelch-like protein 24 isoform a
NM_001349419.1 NP_001336348.1 kelch-like protein 24 isoform b
NM_001349420.1 NP_001336349.1 kelch-like protein 24 isoform b
NM_001349421.1 NP_001336350.1 kelch-like protein 24 isoform b
NM_001349422.1 NP_001336351.1 kelch-like protein 24 isoform b
NM_001349423.1 NP_001336352.1 kelch-like protein 24 isoform b
NM_001349424.1 NP_001336353.1 kelch-like protein 24 isoform b
NM_001349425.1 NP_001336354.1 kelch-like protein 24 isoform b
NM_001349426.1 NP_001336355.1 kelch-like protein 24 isoform b
NM_001349428.1 NP_001336357.1 kelch-like protein 24 isoform c
NM_001349429.1 NP_001336358.1 kelch-like protein 24 isoform c
NM_017644.3 NP_060114.2 kelch-like protein 24 isoform b

KLHL24 Protein Structure

BTB

BTB: BTB/POZ domain (56 - 162)

BACK

BACK: BTB And C-terminal Kelch (168 - 270)

Kelch_1

Kelch_1: Kelch motif (354 - 394)

Kelch_1

Kelch_1: Kelch motif (400 - 440)

Kelch_1

Kelch_1: Kelch motif (445 - 482)

Kelch_1

Kelch_1: Kelch motif (494 - 529)

Kelch_1

Kelch_1: Kelch motif (536 - 578)

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Protein Preferred Names Protein Names

kelch-like protein 24

kainate receptor interacting protein for GluR6

Related Diseases

Diseases Alias
Epidermolysis Bullosa Simplex 6, Generalized, With Scarring And Hair Loss

Epidermolysis Bullosa Simplex, Generalized, With Scarring And Hair Loss

EBS6

Ebssh

Intermediate Epidermolysis Bullosa Simplex With Cardiomyopathy

Intermediate Ebs With Cardiomyopathy
Epidermolysis Bullosa Simplex Generalized Type

Epidermolysis Bullosa Simplex, Koebner Type

Epidermolysis Bullosa Simplex Koebner Type

Epidermolysis Bullosa Simplex, Generalized

Ebs, Generalized

Ebs-K

Epidermolysis Bullosa Simplex, Generalized Non-Dowling-Meara

Generalized Ebs

Epidermolysis Bullosa Simplex Kobner
Epidermolysis Bullosa Simplex

Ebs

Epidermolysis Bullosa Intraepidermic

Epidermolytic Epidermolysis Bullosa
Epidermolysis Bullosa

Acantholysis Bullosa

Eb
Diffuse Palmoplantar Keratoderma

Diffuse Palmoplantar Hyperkeratosis

Diffuse Ppk

Diffuse Keratosis Palmoplantaris
Transient Bullous Dermolysis Of The Newborn

TBDN

Transient Bullous Of The Newborn

Epidermolysis Bullosa Dystrophica, Neonatal Form

Dystrophic Epidermolysis Bullosa, Neonatal

Deb, Bullous Dermolysis Of The Newborn

Deb-Bdn

Epidermolysis Bullosa Dystrophica, Dominant Neonatal Form

Self-Improving Dystrophic Epidermolysis Bullosa

Self-Improving Deb

Epidermolysis Bullosa Dystrophica Dominant Neonatal Type
Ureterocele
Epidermolysis Bullosa Simplex 1a, Generalized Severe

Epidermolysis Bullosa Simplex, Dowling-Meara Type

Epidermolysis Bullosa Herpetiformis, Dowling-Meara Type

EBS1A

Ebsdm

Epidermolysis Bullosa Simplex Dowling-Meara Type

Epidermolysis Bullosa Simplex, Herpetiformis

Ebs-Dm

Epidermolysis Bullosa Simplex 1a, Dowling-Meara Type

Ebs-Gen Sev

Epidermolysis Bullosa Herpetiformis Dowling-Meara Type

Generalized Severe Epidermolysis Bullosa Simplex

Dowling-Meara Type Epidermolysis Bullosa Simplex

Autosomal Dominant Generalized Epidermolysis Bullosa Simplex, Severe Form

Autosomal Dominant Generalized Ebs, Severe Form

Epidermolysis Bullosa Simplex Herpetiformis

Dm-Ebs

Epidermolysis Bullosa Simplex, Generalized Severe

Epidermolysis Bullosa Herpetiformis, Dowling-Meara

Epidermolysis Bullosa Herpetiformis Dowling-Meara
Cold-Induced Sweating Syndrome

Crisponi Syndrome

Sohar-Crisponi Syndrome

Ciss

Cntf Receptor-Related Disorders

Muscle Contractions, Tetanoform, With Characteristic Face, Camptodactyly, Hyperthermia, And Sudden Death

Sweating Syndrome, Cold-Induced
Bullous Skin Disease

Skin Diseases Bullous

Skin Diseases, Bullous
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS07364 KLHL24 Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus KLHL24 VGNC VGNC:63149
Bos taurus KLHL24 VGNC VGNC:30652
Canis familiaris KLHL24 VGNC VGNC:42458
Macaca mulatta KLHL24 VGNC VGNC:74128
Rattus norvegicus KLHL24 RGD RGD:727971
Mus musculus KLHL24 MGD MGI:1923035