Variant ID | 19783 |
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Entrez Gene ID | 284058 |
Gene | KANSL1 (GeneCards) |
Location | hg19 17:44186549-44186549
hg38 17:46109183-46109183 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000017.10:g.44186549 G>A (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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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 | 81195210 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.3581 |
CADD Raw score (version 1.3) | -0.38096 (Deleterious) |
FATHMM raw prediction score | 0.08383 (Tolerated) |
Deleterious probability by DeFine | 0.1155 (Neutral) |
Entrez Gene ID | 284058 (NCBI Gene) |
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Official Gene Symbol | KANSL1 (GeneCards) |
Number of variants in KANSL1 in this database | 4 (view all the variants) |
Full name | KAT8 regulatory NSL complex subunit 1 |
Band | 17q21.31 |
Other IDs | Vega: OTTHUMG00000178026 OMIM: 612452 HGNC: HGNC:24565 Ensembl: ENSG00000120071 |
Other names | KDVS, NSL1, MSL1v1, CENP-36, hMSL1v1, KIAA1267 |
Summary | This gene encodes a nuclear protein that is a subunit of two protein complexes involved with histone acetylation, the MLL1 complex and the NSL1 complex. The corresponding protein in Drosophila interacts with K(lysine) acetyltransferase 8, which is also a subunit of both the MLL1 and NSL1 complexes. [provided by RefSeq, Jun 2012] |
Individual ID | 29217584.02 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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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; |