The BHLHB9 gene homepage

General information
Gene symbol BHLHB9
Gene name basic helix-loop-helix domain containing, class B, 9
Chromosome X
Chromosomal band q23
Imprinted Unknown
Genomic reference NG_021340.1
Transcript reference NM_030639.2
Associated with diseases -
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 23
Unique public DNA variants reported 23
Individuals with public variants 2
Hidden variants 1
Notes This gene sequence variant database has been initiated based on the data reported by Tarpey et al. (2009) A systematic, large-scale resequencing screen of the X-chromosome coding exons in mental retardation. Nat.Genet. 41: 535-543. Establishment of the database was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project.
Date created March 06, 2009
Date last updated May 09, 2022
Version BHLHB9:220509

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
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
HGNC 29353
Entrez Gene 80823
PubMed articles BHLHB9
OMIM - Gene 300921
HGMD BHLHB9
GeneCards BHLHB9
GeneTests BHLHB9
Orphanet BHLHB9


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000904 X transcript variant 2 NM_030639.2 NP_085142.1 23


Copyright & disclaimer
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