The CYP26C1 gene homepage

General information
Gene symbol CYP26C1
Gene name cytochrome P450, family 26, subfamily C, polypeptide 1
Chromosome 10
Chromosomal band q23.33
Imprinted Unknown
Genomic reference NG_007958.1
Transcript reference NM_183374.2
Exon/intron information NM_183374.2 exon/intron table
Associated with diseases FFDD-4
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 16
Unique public DNA variants reported 9
Individuals with public variants 19
Hidden variants 1
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 September 17, 2021
Version CYP26C1:210917

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_183374.2.
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
HGNC 20577
Entrez Gene 340665
PubMed articles CYP26C1
OMIM - Gene 608428
OMIM - Diseases FFDD-4 (dysplasia, dermal, facial, focal, type 4 (FFDD-4))
GeneCards CYP26C1
GeneTests CYP26C1
Orphanet CYP26C1

Active transcripts




NCBI ID     

NCBI Protein ID     

00006049 10 cytochrome P450, family 26, subfamily C, polypeptide 1 NM_183374.2 NP_899230.2 16

Copyright & disclaimer
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