Overview

Variant ID 21450
Entrez Gene ID 55959
Gene SULF2 (GeneCards)
Location hg19 20:46591877-46591877
hg38 20:47963133-47963133
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000020.10:g.46591877 C>A (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 63025520

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.065
CADD Raw score (version 1.3) -0.073957 (Deleterious)
FATHMM raw prediction score 0.18022 (Tolerated)
Deleterious probability by DeFine 0.4257 (Neutral)
Entrez Gene ID 55959 (NCBI Gene)
Official Gene Symbol SULF2 (GeneCards)
Number of variants in SULF2 in this database 6 (view all the variants)
Full name sulfatase 2
Band 20q13.12
Other IDs Vega: OTTHUMG00000032675
OMIM: 610013
HGNC: HGNC:20392
Ensembl: ENSG00000196562
Other names HSULF-2
Summary Heparan sulfate proteoglycans (HSPGs) act as coreceptors for numerous heparin-binding growth factors and cytokines and are involved in cell signaling. Heparan sulfate 6-O-endosulfatases, such as SULF2, selectively remove 6-O-sulfate groups from heparan sulfate. This activity modulates the effects of heparan sulfate by altering binding sites for signaling molecules (Dai et al., 2005 [PubMed 16192265]).[supplied by OMIM, Mar 2008]

Individual #1

Individual ID 29217584.15 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;