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Kat6b Gene Detail
Summary
  • Symbol
    Kat6b
  • Name
    K(lysine) acetyltransferase 6B
  • Synonyms
    B130044K16Rik, monocytic leukemia, Morf, Myst4, qkf, querkopf
  • Feature Type
    protein coding gene
  • IDs
    MGI:1858746
    NCBI Gene: 54169
  • Gene Overview
    MyGene.info: KAT6B
  • Alliance
    gene page
Location & Maps
more
  • Sequence Map
    Chr14:21481434-21672478 bp, + strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser
  • Download
    Sequence
      191045 bp   ±  kb flank

  • Genome Browsers
    VEGA | Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 14, 11.73 cM
  • Mapping Data
    2 experiments
Homology
more
  • Human Ortholog
    KAT6B, lysine acetyltransferase 6B
  • Vertebrate Orthologs
    2
  • Human Ortholog
    KAT6B, lysine acetyltransferase 6B
    Orthology source: HGNC
  • Synonyms
    GTPTS, MORF, MOZ2, MYST4, qkf, querkopf, ZC2HC6B
  • Links
    NCBI Gene ID: 23522
    neXtProt AC: NX_Q8WYB5
    UniProt: Q8WYB5

  • Chr Location
    10q22.2; chr10:74824927-75032623 (+)  GRCh38.p7
Human Diseases
more
  • Diseases
    1 with Kat6b mouse models; 1 with human KAT6B associations

Human Disease Mouse Models
      
IDs
 View 1 model
      
IDs
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    29 phenotypes from 2 alleles in 2 genetic backgrounds
    16 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Reduced expression of this gene results in developmental defects of the skeleton and brain, particularly the cerebral cortex.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    16
  • GO References
    5
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
receptor binding
RNA binding
transcription
transferase
transporter
Biological Process

nucleic acid-templated transcription
carbohydrate derivative metabolism
cell death
cell differentiation
cell proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
synapse
vacuole
Click cells to view annotations.
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
    74
  • Tissues
    40
  • cDNA Data
    123
  • Literature Summary
    12
  • Comparison Matrix
    Gene Expression + Phenotype
    • Interactions
    less
    Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic OTTMUSG00000043207 VEGA Gene Model | MGI Sequence Detail 191045 C57BL/6J ±  kb
    transcript OTTMUST00000113320 VEGA | MGI Sequence Detail 7660 Not Applicable  
    polypeptide OTTMUSP00000063398 VEGA | MGI Sequence Detail 1872 Not Applicable  
    For the selected sequence
    Polymorphisms
    less
    • SNPs within 2kb
      1028 from dbSNP Build 142
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 125
      cDNA 123
      Primer pair 2

      Microarray probesets 5
    Other
    Accession IDs
    less
    MGI:2145668, MGI:2443197
    References
    more
    • Summaries
      All 51
      Developmental Gene Expression 12
      Diseases 1
      Gene Ontology 5
      Phenotypes 16
    • Earliest
      J:93290 Araki K, et al., Exchangeable gene trap using the Cre/mutated lox system. Cell Mol Biol (Noisy-Le-Grand). 1999 Jul;45(5):737-50
    • Latest
      J:236440 You L, et al., The chromatin regulator Brpf1 regulates embryo development and cell proliferation. J Biol Chem. 2015 May 1;290(18):11349-64
    Contributing Projects:
    Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
    Citing These Resources
    Funding Information
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    Send questions and comments to User Support.     		last database update
    06/12/2018
    MGI 6.12     		The Jackson Laboratory