Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55295
Gene name Gene Name - the full gene name approved by the HGNC.
Kelch like family member 26
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KLHL26
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.11
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT723879 hsa-miR-490-3p HITS-CLIP 19536157
MIRT723878 hsa-miR-649 HITS-CLIP 19536157
MIRT723877 hsa-miR-3155a HITS-CLIP 19536157
MIRT723876 hsa-miR-3155b HITS-CLIP 19536157
MIRT723875 hsa-miR-484 HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25036637, 32296183, 32814053, 33961781
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q53HC5
Protein name Kelch-like protein 26
Protein function May play a role in endo(sarco)plasmic reticulum (ER/SR) mitochondrial signaling (PubMed:37204873). May be part of the ubiquitin-proteasome system (UPS) and affect ubiquitination and degradation of target substrates in cardiomyocytes (PubMed:3720
PDB 9ETW
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00651 BTB 53 159 BTB/POZ domain Domain
PF07707 BACK 165 266 BTB And C-terminal Kelch Domain
PF01344 Kelch_1 402 442 Kelch motif Repeat
PF01344 Kelch_1 452 495 Kelch motif Repeat
PF01344 Kelch_1 497 546 Kelch motif Repeat
PF01344 Kelch_1 550 590 Kelch motif Repeat
Sequence
Sequence length 615
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Gastroesophageal Reflux Disease Gastroesophageal reflux disease N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Ebstein Anomaly Associate 31985165, 37204873
Noncompaction of Left Ventricular Myocardium Familial Isolated Autosomal Dominant 1 Associate 31985165, 37204873