The PHOX2B gene homepage

General information
Gene symbol PHOX2B
Gene name paired-like homeobox 2b
Chromosome 4
Chromosomal band p13
Imprinted Unknown
Genomic reference NG_008243.1
Transcript reference NM_003924.3
Exon/intron information NM_003924.3 exon/intron table
Associated with diseases CCHS, NBLST2
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 139
Unique public DNA variants reported 71
Individuals with public variants 475
Hidden variants 5
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 April 19, 2024
Version PHOX2B:240419

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_003924.3.
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 http://www.LOVD.nl/PHOX2B
HGNC 9143
Entrez Gene 8929
PubMed articles PHOX2B
OMIM - Gene 603851
OMIM - Diseases CCHS (hypoventilation, central, syndrome, congenital, with/without Hirschsprung disease (CCHS1))
NBLST2 (neuroblastoma, susceptibility to, type 2 (NBLST-2))
HGMD PHOX2B
GeneCards PHOX2B
GeneTests PHOX2B
Orphanet PHOX2B


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00016114 4 paired-like homeobox 2b NM_003924.3 NP_003915.2 139


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