The KLHL41 gene homepage

General information
Gene symbol KLHL41
Gene name kelch-like family member 41
Chromosome 2
Chromosomal band q31.1
Imprinted Unknown
Genomic reference NC_000002.11
Transcript reference NM_006063.2
Exon/intron information NM_006063.2 exon/intron table
Associated with diseases NEM, NEM9
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Johan den Dunnen
Total number of public variants reported 20
Unique public DNA variants reported 17
Individuals with public variants 53
Hidden variants -
Notes alias KBTBD10, SARCOSIN
This database is one of the gene variant databases from the "Leiden Muscular Dystrophy pages" (LMDp)
Date created December 22, 2014
Date last updated November 23, 2023
Version KLHL41:231123

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_006063.2.
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 http://www.LOVD.nl/KLHL41
HGNC 16905
Entrez Gene 10324
PubMed articles KLHL41
OMIM - Gene 607701
OMIM - Diseases NEM9 (myopathy, nemaline, type 9 (NEM-9))
HGMD KLHL41
GeneCards KLHL41
GeneTests KLHL41
Orphanet KLHL41


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00023996 2 kelch-like family member 41 NM_006063.2 NP_006054.2 20


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