The C4orf22 gene homepage

NOTE: gene symbol was recently changed from C4orf22 to CFAP299.
General information
Gene symbol C4orf22
Gene name chromosome 4 open reading frame 22
Chromosome 4
Chromosomal band q21.21
Imprinted Unknown
Genomic reference NC_000004.11
Transcript reference NM_001206997.1
Exon/intron information NM_001206997.1 exon/intron table
Associated with diseases -
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 1
Unique public DNA variants reported 1
Individuals with public variants 0
Hidden variants -
Download all this gene's data Download all data
Notes NOTE: gene symbol was recently changed from C4orf22 to CFAP299.
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 June 16, 2020
Version C4orf22:200616

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_001206997.1.
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/CFAP299
HGNC HGNC:28554
Entrez Gene 255119
PubMed articles C4orf22
HGMD C4orf22
GeneCards C4orf22
NIH Genetic Testing Registry C4orf22
Orphanet C4orf22


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00025272 4 transcript variant 1 NM_001206997.1 NP_001193926.1 1


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