The VLDLR gene homepage

General information
Gene symbol VLDLR
Gene name very low density lipoprotein receptor
Chromosome 9
Chromosomal band p24
Imprinted Unknown
Genomic reference NG_012741.1
Transcript reference NM_003383.3
Exon/intron information NM_003383.3 exon/intron table
Associated with diseases CAMRQ, CAMRQ1, ID
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 77
Unique public DNA variants reported 73
Individuals with public variants 160
Hidden variants 10
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated May 09, 2022
Version VLDLR:220509

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_003383.3.
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
HGNC 12698
Entrez Gene 7436
PubMed articles VLDLR
OMIM - Gene 192977
OMIM - Diseases CAMRQ1 (ataxia, cerebellar, mental retardation, quadrupedal locomotion, type 1 (CAMRQ-1))
GeneCards VLDLR
GeneTests VLDLR
Orphanet VLDLR

Active transcripts




NCBI ID     

NCBI Protein ID     

00024091 9 transcript variant 1 NM_003383.3 NP_003374.3 77

Copyright & disclaimer
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