The HMGCL gene homepage

General information
Gene symbol HMGCL
Gene name 3-hydroxymethyl-3-methylglutaryl-CoA lyase
Chromosome 1
Chromosomal band p36.1-p35
Imprinted Unknown
Genomic reference NG_013061.1
Transcript reference NM_000191.2
Exon/intron information NM_000191.2 exon/intron table
Associated with diseases HMGCLD
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 194
Unique public DNA variants reported 72
Individuals with public variants 183
Hidden variants 2
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated July 07, 2023
Version HMGCL:230707

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_000191.2.
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/HMGCL
HGNC 5005
Entrez Gene 3155
PubMed articles HMGCL
OMIM - Gene 613898
OMIM - Diseases HMGCLD (HMG-CoA lyase deficiency)
HGMD HMGCL
GeneCards HMGCL
GeneTests HMGCL
Orphanet HMGCL


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00009472 1 transcript variant 1 NM_000191.2 NP_000182.2 194


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