The EDNRB gene homepage

General information
Gene symbol EDNRB
Gene name endothelin receptor type B
Chromosome 13
Chromosomal band q22
Imprinted Unknown
Genomic reference NG_011630.3
Transcript reference NM_000115.3, NM_001122659.2
Exon/intron information NM_000115.3 exon/intron table
Associated with diseases ABCDS, HSCR2, WS, WS4A
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Veronique Pingault
Total number of public variants reported 120
Unique public DNA variants reported 97
Individuals with public variants 86
Hidden variants 10
Download all this gene's data Download all data
Notes Initiated as Waardenburg syndrome gene variant databases by Veronique Pingault.
Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created October 05, 2009
Date last updated November 27, 2023
Version EDNRB:231127

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_000115.3.
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 https://www.LOVD.nl/EDNRB
HGNC 3180
Entrez Gene 1910
PubMed articles EDNRB
OMIM - Gene 131244
OMIM - Diseases ABCDS (ABCD syndrome (ABCDS))
HSCR2 (Hirschsprung disease, susceptibility to, type 2 (HSCR-2))
WS4A (Waardenburg syndrome, type 4A (WS4A))
HGMD EDNRB
GeneCards EDNRB
GeneTests EDNRB
Orphanet EDNRB


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00006875 13 transcript variant 1 NM_000115.3 NP_000106.1 119
00025878 13 transcript variant 3 NM_001122659.2 NP_001116131.1 35


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