The WHSC1L1 gene homepage

General information
Gene symbol WHSC1L1
Gene name Wolf-Hirschhorn syndrome candidate 1-like 1
Chromosome 8
Chromosomal band p11.2
Imprinted Unknown
Genomic reference NG_023292.1
Transcript reference NM_017778.2, NM_023034.1, XM_005273547.1, XM_005273548.1
Associated with diseases AML
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 39
Unique public DNA variants reported 8
Individuals with public variants 27
Hidden variants 7
Date created October 30, 2013
Date last updated September 23, 2016
Version WHSC1L1:160923

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
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:12767
Entrez Gene 54904
PubMed articles WHSC1L1
OMIM - Gene 607083
OMIM - Diseases AML (leukemia, myeloid, acute (AML))
HGMD WHSC1L1
GeneCards WHSC1L1
GeneTests WHSC1L1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00008757 8 transcript variant long NM_023034.1 NP_075447.1 21
00008758 8 transcript variant short NM_017778.2 NP_060248.2 21
00047184 8 transcript variant X2 XM_005273548.1 XP_005273605.1 -
00047185 8 transcript variant X1 XM_005273547.1 XP_005273604.1 -


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