Variant ID | 19483 |
---|---|
Entrez Gene ID | 6299 |
Gene | SALL1 (GeneCards) |
Location | hg19 16:51409132-51409132
hg38 16:51375221-51375221 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000016.9:g.51409132 G>A (Genome Assembly: GRCh37) |
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 | 90354753 |
MAF in gnomAD genome (version 2.0.1) | 0 |
---|---|
EIGEN score | -0.3809 |
CADD Raw score (version 1.3) | -0.21509 (Deleterious) |
FATHMM raw prediction score | 0.09634 (Tolerated) |
Deleterious probability by DeFine | 0.5611 (Deleterious) |
Entrez Gene ID | 6299 (NCBI Gene) |
---|---|
Official Gene Symbol | SALL1 (GeneCards) |
Number of variants in SALL1 in this database | 95 (view all the variants) |
Full name | spalt like transcription factor 1 |
Band | 16q12.1 |
Other IDs | Vega: OTTHUMG00000133176 OMIM: 602218 HGNC: HGNC:10524 Ensembl: ENSG00000103449 |
Other names | TBS, HSAL1, Sal-1, ZNF794, HEL-S-89 |
Summary | The protein encoded by this gene is a zinc finger transcriptional repressor and may be part of the NuRD histone deacetylase complex (HDAC). Defects in this gene are a cause of Townes-Brocks syndrome (TBS) as well as bronchio-oto-renal syndrome (BOR). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.09 (view all the variants in this individual) |
---|---|
Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
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; |