The KBTBD13 gene homepage

This database is one of the gene variant databases from the Leiden Muscular Dystrophy pages
General information
Gene symbol KBTBD13
Gene name kelch repeat and BTB (POZ) domain containing 13
Chromosome 15
Chromosomal band q22.31
Imprinted Unknown
Genomic reference NG_021411.1
Transcript reference NM_001101362.2
Exon/intron information NM_001101362.2 exon/intron table
Associated with diseases NEM6
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Johan den Dunnen
Total number of public variants reported 76
Unique public DNA variants reported 48
Individuals with public variants 76
Hidden variants 13
Download all this gene's data Download all data
Notes This database is one of the gene variant databases from the:
Date created December 11, 2010
Date last updated April 19, 2024
Version KBTBD13:240419

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001101362.2.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/KBTBD13
HGNC 37227
Entrez Gene 390594
PubMed articles KBTBD13
OMIM - Gene 613727
OMIM - Diseases NEM6 (myopathy, nemaline, type 6 (NEM-6))
HGMD KBTBD13
GeneCards KBTBD13
GeneTests KBTBD13
Orphanet KBTBD13


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00010323 15 kelch repeat and BTB (POZ) domain containing 13 NM_001101362.2 NP_001094832.1 76


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