KAT6B (GeneID: 23522) | Homo sapiens
Description: lysine acetyltransferase 6B [Source:HGNC Symbol;Acc:HGNC:17582]
Synonyms: querkopf, MOZ2, C2HC6B, qkf, MORF, MYST4, GTPTS
Other ID(s): ENSG00000281813, ENSG00000156650, HGNC:17582
Protein Accession Numbers: ENST00000372725, NP_001357066, NP_036462, ENST00000372711, NP_001357063, NP_001357071, NP_001243398, NP_001357068, ENST00000372724, NP_001357065, NP_001357073, ENST00000287239, NP_001357062, NP_001357070, NP_001243397, NP_001357067, ENST00000372714, NP_001357064, NP_001357072, NP_001357061, NP_001357069
Statistics: ClinVar(920) gnomAD(3747) COSMIC(2380)
ClinVar Pathogenicity of Variations help

∙ 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.
ENST00000287239 ENST00000372711 ENST00000372714 You are here now! ENST00000372724 You are here now! ENST00000372725 You are here now! NP_001243397 NP_001243398 You are here now! NP_001357061 NP_001357062 NP_001357063 NP_001357064 NP_001357065 NP_001357066 NP_001357067 NP_001357068 You are here now! NP_001357069 You are here now! NP_001357070 You are here now! NP_001357071 You are here now! NP_001357072 NP_001357073 NP_036462


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
NO DOMAINS EXIST

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Arthrogryposis Musculoskeletal Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; 0.565 0.69
Malignant neoplasm of breast Neoplasms ; Skin and Connective Tissue Diseases ; 0.565 0.69
Noonan Syndrome Musculoskeletal Diseases ; Cardiovascular Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Skin and Connective Tissue Diseases ; 0.565 0.69
Juvenile-Onset Still Disease Musculoskeletal Diseases ; Skin and Connective Tissue Diseases ; Immune System Diseases ; 0.565 0.69
Bipolar I disorder N/A 0.565 0.69
Genitopatellar Syndrome Musculoskeletal Diseases ; Nervous System Diseases ; Male Urogenital Diseases ; Female Urogenital Diseases and Pregnancy Complications ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.565 0.69
Young Simpson syndrome Musculoskeletal Diseases ; Nervous System Diseases ; Eye Diseases ; Cardiovascular Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; Endocrine System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.565 0.69
Juvenile arthritis Musculoskeletal Diseases ; Skin and Connective Tissue Diseases ; Immune System Diseases ; 0.565 0.69
Intellectual Disability Nervous System Diseases ; Pathological Conditions, Signs and Symptoms ; Behavior and Behavior Mechanisms ; Mental Disorders ; 0.565 0.69
Juvenile psoriatic arthritis Musculoskeletal Diseases ; Skin and Connective Tissue Diseases ; Immune System Diseases ; 0.565 0.69
NO RESULT FOUND
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