Variant ID | 29146 |
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Entrez Gene ID | 23522 |
Gene | KAT6B (GeneCards) |
Location | hg19 10:76789588-76789588
hg38 10:75029830-75029830 |
Disease | Autism Spectrum Disorders (view all the variants in this disease) |
Method | PASM |
Mutation(HGVS format) | NC_000010.10:g.76789588 A>G (Genome Assembly: GRCh37) |
Exon or Intron | Exon |
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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 | 135534747 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.6548 |
CADD Raw score (version 1.3) | 5.653205 (Deleterious) |
FATHMM raw prediction score | 0.95949 (Tolerated) |
SIFT score | 0 (Deleterious) |
LRT score | 0 (Deleterious) |
MutationTaster score | 1 (Deleterious) |
MutatioinAssessor score | 0.805 (Tolerated) |
PROVEAN score | -5.12 (Deleterious) |
MetaSVM score | 0.598 (Deleterious) |
MetaLR score | 0.723 (Deleterious) |
MCAP score | 0.261 (Deleterious) |
FitCons score | 0.732 (Highly Significant p < 0.003 ) |
Genomic Evolutionary Rate Profiling (GERP) score | 5.17 |
PhyloP score based on multiple alignment of 100 vertebrates | 8.947 |
PhastCons score based on multiple alignment of 100 vertebrates | 1 |
SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 14.997 |
Deleterious probability by iFish2 | 0.9811 (Deleterious) |
Deleterious probability by DeFine | 0.9409 (Deleterious) |
Entrez Gene ID | 23522 (NCBI Gene) |
---|---|
Official Gene Symbol | KAT6B (GeneCards) |
Number of variants in KAT6B in this database | 2 (view all the variants) |
Full name | lysine acetyltransferase 6B |
Band | 10q22.2 |
Other IDs | Vega: OTTHUMG00000018509 OMIM: 605880 HGNC: HGNC:17582 Ensembl: ENSG00000156650 |
Other names | qkf, MORF, MOZ2, GTPTS, MYST4, ZC2HC6B, qerkopf |
Summary | The protein encoded by this gene is a histone acetyltransferase and component of the MOZ/MORF protein complex. In addition to its acetyltransferase activity, the encoded protein has transcriptional activation activity in its N-terminal end and transcriptional repression activity in its C-terminal end. This protein is necessary for RUNX2-dependent transcriptional activation and could be involved in brain development. Mutations have been found in patients with genitopatellar syndrome. A translocation of this gene and the CREBBP gene results in acute myeloid leukemias. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2012] |
Individual ID | 28503910.23 (view all the variants in this individual) |
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Pubmed ID | 28503910 |
Whose mosaic mutation | Patient |
Phenotype | 3 |
Disease | Autism Spectrum Disorders (view all the variants in this disease) |
OMIM ID | 209850 |
Pubmed ID | 28503910 |
---|---|
Title | Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations |
Journal | Human Mutation |
Publication date | 2017.05 |
Disease | Autism Spectrum Disorders |
Incidence | 0.01 |
Number of cases | cases of unknown sex: 215; |