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 32296183, 32814053
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
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Gastroesophageal Reflux Disease Gastroesophageal Reflux Disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Ebstein Anomaly Associate 31985165, 37204873
Noncompaction of Left Ventricular Myocardium Familial Isolated Autosomal Dominant 1 Associate 31985165, 37204873