The CHST8 gene homepage

General information
Gene symbol CHST8
Gene name carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 8
Chromosome 19
Chromosomal band q13.1
Imprinted Unknown
Genomic reference NG_029857.1
Transcript reference NM_001127895.1
Exon/intron information NM_001127895.1 exon/intron table
Associated with diseases PSS3
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 5
Unique public DNA variants reported 5
Individuals with public variants 1
Hidden variants -
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created August 22, 2011
Date last updated September 15, 2020
Version CHST8:200915

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_001127895.1.
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/CHST8
HGNC 15993
Entrez Gene 64377
PubMed articles CHST8
OMIM - Gene 610190
OMIM - Diseases PSS3 (skin, peeling? syndrome, type 3 (PSS-3))
HGMD CHST8
GeneCards CHST8
GeneTests CHST8
Orphanet CHST8


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000684 19 transcript variant 1 NM_001127895.1 NP_001121367.1 5


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