KAT6A (GeneID: 7994) | Homo sapiens
Description: lysine acetyltransferase 6A [Source:HGNC Symbol;Acc:HGNC:13013]
Synonyms: ZNF220, MYST-3, C2HC6A, RUNXBP2, MRD32, MYST3, MOZ
Other ID(s): HGNC:13013, ENSG00000083168
Protein Accession Numbers: ENST00000485568, ENST00000406337, NP_006757, ENST00000426524, ENST00000396930, NP_001292807, ENST00000418721, ENST00000265713
Statistics:

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000265713 ENST00000396930 ENST00000406337 ENST00000418721 ENST00000426524 ENST00000485568 NP_001292807 NP_006757


import_contactsClinVar Data
Variation ID filter_list Allele ID filter_list RS Number filter_list Variant Type filter_list Record filter_list Alteration filter_list Clinicial Sig. filter_list Last Update filter_list Phenotypes filter_list Cytogenetic filter_list Review Status filter_list RCV Acc.N. filter_list

healinggnomAD
Variant ID filter_list Transcript ID filter_list Alteration filter_list Annotation filter_list Allele C. filter_list Allele N. filter_list Allele F. filter_list rsNumber filter_list Flagsfilter_list Filter filter_list

placePost-translational Modifications (PTMs)
Gene Name filter_list ACC ID filter_list PTM Type filter_list Position filter_list Mod-rsd filter_list Site +/-7 Aa filter_list Mw_kd filter_list Site grpID filter_list

blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
Gene Name filter_list Transcript ID filter_list Sample name filter_list Primary Site filter_list Primary Histology filter_list Mutation ID filter_list Mutation CDS filter_list Mutation Aa filter_list Mutation Desc. filter_list FATHMM Prediction filter_list FATHMM Score filter_list Mutation Somatic Status filter_list PUBMED PMID filter_list Tumor Origin filter_list Position filter_list

chrome_reader_modedbSNP
Gene ID filter_list Transcript ID filter_list Consequence filter_list Position filter_list HGVSp filter_list Impact filter_list

format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
PF00628 PHD PHD-finger 264-313 CL0390 zf-FYVE-PHD Mus musculus
PF00628 PHD PHD-finger 208-265 CL0390 zf-FYVE-PHD Mus musculus
PF01853 MOZ_SAS MOZ/SAS family 564-742 CL0257 Acetyltrans Mus musculus
PF17772 zf-MYST MYST family zinc finger domain 505-559 CL0361 C2H2-zf Mus musculus

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Craniosynostosis Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.602 0.517
Adenoid Cystic Carcinoma Neoplasms ; 0.602 0.517
Medulloblastoma Neoplasms ; 0.602 0.517
Prostatic Neoplasms Neoplasms ; Male Urogenital Diseases ; 0.602 0.517
Medullomyoblastoma Neoplasms ; 0.602 0.517
Childhood Medulloblastoma Neoplasms ; 0.602 0.517
Adult Medulloblastoma Neoplasms ; 0.602 0.517
Malignant neoplasm of prostate Neoplasms ; Male Urogenital Diseases ; 0.602 0.517
Desmoplastic Medulloblastoma Neoplasms ; 0.602 0.517
Melanotic medulloblastoma Neoplasms ; 0.602 0.517
Intellectual Disability Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.602 0.517
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 N/A 0.602 0.517
Acute myeloid leukemia with t(8;16)(p11;p13) translocation N/A 0.602 0.517
NO RESULT FOUND
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