The NHSL2 gene homepage

General information
Gene symbol NHSL2
Gene name NHS-like 2
Chromosome X
Chromosomal band q13.1
Imprinted Unknown
Genomic reference NG_029583.1
Transcript reference NM_001013627.2
Associated with diseases -
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 67
Unique public DNA variants reported 52
Individuals with public variants 5
Hidden variants 16
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 November 10, 2009
Date last updated February 26, 2024
Version NHSL2:240226

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 33737
Entrez Gene 340527
PubMed articles NHSL2
HGMD NHSL2
GeneCards NHSL2
GeneTests NHSL2
Orphanet NHSL2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000392 X NHS-like 2 NM_001013627.2 NP_001013649.2 67


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