H2BFWT gene homepage

General information
Gene symbol H2BFWT
Gene name H2B histone family, member W, testis-specific
Chromosome X
Chromosomal band q22.2
Imprinted Unknown
Genomic reference NG_016406.1
Transcript reference NM_001002916.3
Associated with diseases -
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 8
Unique public DNA variants reported 6
Individuals with public variants 10
Hidden variants 0
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 August 17, 2018
Version H2BFWT:180817

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 27252
Entrez Gene 158983
PubMed articles H2BFWT
OMIM - Gene 300507
HGMD H2BFWT
GeneCards H2BFWT
GeneTests H2BFWT


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000803 X H2B histone family, member W, testis-specific NM_001002916.3 NP_001002916.2 8


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