ACADVL homepage - CCHMC Molecular Genetics Laboratory Mutation Database - Leiden Open Variation Database

CCHMC Molecular Genetics Laboratory Mutation Database

VLCAD acyl-Coenzyme A dehydrogenase, very long chain (ACADVL)

LOVD v.2.0 Build 36 [ Current LOVD status ]
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Curator: Ammar Husami

ACADVL homepage

General information
Gene name	VLCAD acyl-Coenzyme A dehydrogenase, very long chain
Gene symbol	ACADVL
Chromosome Location	17p13.1
Database location	https://research.cchmc.org/LOVD2/
Curator	Ammar Husami
PubMed references	View all (unique) PubMed references in the ACADVL database
Date of creation	April 27, 2010
Last update	April 27, 2010
Version	ACADVL100427
Add sequence variant	Submit a sequence variant
First time submitters	Register here
Reference sequence file	coding DNA reference sequence for describing sequence variants
Genomic refseq ID	NG_007975.1
Transcript refseq ID	NM_000018.2
Exon/intron information	Exon/intron information table
Total number of unique DNA variants reported	81
Total number of individuals with variant(s)	2
Total number of variants reported	84
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Graphical displays and utilities
Summary tables	Summary of all sequence variants in the ACADVL database, sorted by type of variant (with graphical displays and statistics)
Reading-frame checker	The Reading-frame checker generates a prediction of the effect of whole-exon changes
UCSC Genome Browser	Show variants in the UCSC Genome Browser (compact view)
Ensembl Genome Browser	Show variants in the Ensembl Genome Browser (compact view)
NCBI Sequence Viewer	Show distribution histogram of variants in the NCBI Sequence Viewer

Sequence variant tables
Unique sequence variants	Listing of all unique sequence variants in the ACADVL database, without patient data
Complete sequence variant listing	Listing of all sequence variants in the ACADVL database
Variants with no known pathogenicity	Listing of all ACADVL variants reported to have no noticeable phenotypic effect (note: excluding variants of unknown effect)

Search the database
By type of variant	View all sequence variants of a certain type
Simple search	Query the database by selecting the most important variables (exon number, type of variant, disease phenotype)
Advanced search	Query the database by selecting a combination of variables
Based on patient origin	View all variants based on your patient origin search terms

Links to other resources
HGNC	92
Entrez Gene	37
OMIM - Gene	609575
UniProtKB (SwissProt/TrEMBL)	P49748
HGMD	ACADVL
GeneCards	ACADVL
GeneTests	ACADVL