KAT6B Chromosome 10

Lysine acetyltransferase 6B
262 variants 262 Health Risk

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What This Gene Does
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]
Gene Info
Gene Group
"PHD finger proteins|MYST type domain containing lysine acetyltransferases|Zinc fingers MYST C2HC-type"
Locus Type
gene with protein product
Location
10q22.2
Ensembl
ENSG00000156650
Associated Conditions (37)
Genitopatellar syndrome
Blepharophimosis - intellectual disability syndrome
SBBYS type
Inborn genetic diseases
Autosomal dominant KAT6B-related disorders
KAT6B-related disorder
9 conditions
Intellectual disability
Developmental disorder
KAT6B-related multiple congenital anomalies syndrome
Left ventricular noncompaction
Hypospadias
Seizure
Macrocephaly
Generalized joint hypermobility
Joint laxity
Delayed speech and language development
Hepatocellular carcinoma
10 conditions
Chromatinopathy
+17 more conditions
Key Variants
RS1014954135
Conflicting classifications of pathogenicity
Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
Health Risk
RS1019373559
Conflicting classifications of pathogenicity
Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
Health Risk
RS1054836015
Conflicting classifications of pathogenicity
Blepharophimosis - intellectual disability syndrome, SBBYS type, Genitopatellar syndrome
Health Risk
RS1057520090
Conflicting classifications of pathogenicity
Genitopatellar syndrome, Genitopatellar syndrome
Health Risk
RS11001247
Conflicting classifications of pathogenicity
Genitopatellar syndrome, Genitopatellar syndrome
Health Risk
RS113566014
Conflicting classifications of pathogenicity
Inborn genetic diseases, Genitopatellar syndrome, Inborn genetic diseases
Health Risk
RS1167009272
Conflicting classifications of pathogenicity
Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
Health Risk
RS1213787718
Conflicting classifications of pathogenicity
Genitopatellar syndrome, Genitopatellar syndrome
Health Risk
RS1222902525
Conflicting classifications of pathogenicity
Genitopatellar syndrome, Genitopatellar syndrome
Health Risk
RS1265658401
Conflicting classifications of pathogenicity
Genitopatellar syndrome, Inborn genetic diseases, Genitopatellar syndrome
Health Risk
RS1273966358
Conflicting classifications of pathogenicity
Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
Health Risk
RS1274585455
Conflicting classifications of pathogenicity
Genitopatellar syndrome, Inborn genetic diseases, Genitopatellar syndrome
Health Risk
All Variants (262)
RSID Category Clinical Significance Conditions
RS766989154 Health Risk Conflicting classifications of pathogenicity Intellectual disability, Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome
RS767796290 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Genitopatellar syndrome, Inborn genetic diseases
RS768502700 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Inborn genetic diseases, Genitopatellar syndrome
RS769903041 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, KAT6B-related disorder, Genitopatellar syndrome
RS770143760 Health Risk Conflicting classifications of pathogenicity Hypospadias, Inborn genetic diseases, Hypospadias
RS770325540 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Genitopatellar syndrome
RS770958025 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome
RS771834072 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Genitopatellar syndrome
RS772132735 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
RS772530975 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
RS773318837 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
RS773473193 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
RS773778673 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Genitopatellar syndrome
RS774022852 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Inborn genetic diseases, Genitopatellar syndrome
RS774598396 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
RS776774212 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Genitopatellar syndrome
RS777180869 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
RS777433819 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Inborn genetic diseases, Genitopatellar syndrome
RS777567666 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Genitopatellar syndrome, Inborn genetic diseases
RS778899637 Health Risk Conflicting classifications of pathogenicity Seizure, Macrocephaly, Generalized joint hypermobility
RS779662050 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
RS780418110 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
RS781631671 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Inborn genetic diseases, Hepatocellular carcinoma
RS903839861 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Inborn genetic diseases, Blepharophimosis - intellectual disability syndrome
RS935089030 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Inborn genetic diseases, Genitopatellar syndrome
RS965354059 Health Risk Conflicting classifications of pathogenicity Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
RS1554835864 Health Risk Likely pathogenic
RS1554844486 Health Risk Likely pathogenic 10 conditions, 10 conditions
RS1554845880 Health Risk Likely pathogenic Blepharophimosis - intellectual disability syndrome, SBBYS type, Blepharophimosis - intellectual disability syndrome
RS1554846499 Health Risk Likely pathogenic
RS1589824871 Health Risk Likely pathogenic
RS1589824884 Health Risk Likely pathogenic
RS1589844927 Health Risk Likely pathogenic Genitopatellar syndrome, Genitopatellar syndrome
RS1842099343 Health Risk Likely pathogenic Genitopatellar syndrome, Genitopatellar syndrome
RS1842977002 Health Risk Likely pathogenic
RS1845433207 Health Risk Likely pathogenic Blepharophimosis - intellectual disability syndrome, SBBYS type, Genitopatellar syndrome
RS1846092532 Health Risk Likely pathogenic Genitopatellar syndrome, Blepharophimosis - intellectual disability syndrome, SBBYS type
RS1846100784 Health Risk Likely pathogenic Autosomal dominant KAT6B-related disorders, Autosomal dominant KAT6B-related disorders
RS1846182844 Health Risk Likely pathogenic Chromatinopathy, Chromatinopathy
RS2133653927 Health Risk Likely pathogenic
RS2133689570 Health Risk Likely pathogenic
RS2134159675 Health Risk Likely pathogenic Genitopatellar syndrome, Genitopatellar syndrome
RS2134234642 Health Risk Likely pathogenic Genitopatellar syndrome, Genitopatellar syndrome
RS2134236431 Health Risk Likely pathogenic See cases, See cases
RS2134239492 Health Risk Likely pathogenic Genitopatellar syndrome, Genitopatellar syndrome
RS2134240152 Health Risk Likely pathogenic Blepharophimosis - intellectual disability syndrome, SBBYS type, Blepharophimosis - intellectual disability syndrome
RS2134241204 Health Risk Likely pathogenic Blepharophimosis - intellectual disability syndrome, SBBYS type, Blepharophimosis - intellectual disability syndrome
RS2134245408 Health Risk Likely pathogenic
RS2548332680 Health Risk Likely pathogenic Blepharophimosis - intellectual disability syndrome, SBBYS type, Blepharophimosis - intellectual disability syndrome
RS2548333540 Health Risk Likely pathogenic Blepharophimosis - intellectual disability syndrome, SBBYS type, Blepharophimosis - intellectual disability syndrome
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