LOVD CYP4V2 homepage

General information
Gene name cytochrome P450, family 4, subfamily V, polypeptide 2
Gene symbol CYP4V2
Chromosome Location 4q35.2
Database location grenada.lumc.nl
Curator LOVD-team, but with Curator vacancy
PubMed references View all (unique) PubMed references in the CYP4V2 database
Date of creation July 16, 2012
Last update October 03, 2013
Version CYP4V2 131003
Add sequence variant Submit a sequence variant
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Reference sequence file Genomic reference sequence for describing sequence variants
Genomic refseq ID NG_007965.1
Transcript refseq ID NM_207352.3
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 0
Total number of individuals with variant(s) 0
Total number of variants reported 0
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Graphical displays and utilities
Summary tables Summary of all sequence variants in the CYP4V2 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

Links to other resources
HGNC 23198
Entrez Gene 285440
OMIM - Gene 608614
OMIM - Disease Bietti crystalline corneoretinal dystrophy
UniProtKB (SwissProt/TrEMBL) Q6ZWL3
GeneCards CYP4V2
GeneTests CYP4V2