Michael. Kraft, et.al., Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome-like phenotype and hyperactivated MAPK signaling in humans and mice., The Journal of clinical investigation, 2011, 121

http://rdf.ncbi.nlm.nih.gov/pubmed/21804188

Michael. Kraft, et.al., Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome-like phenotype and hyperactivated MAPK signaling in humans and mice., The Journal of clinical investigation, 2011, 121

pubmed

表現型アノテーション

http://purl.org/net/cito/citesAsAuthority

• delayed suture closure_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0010743I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• decreased percent body fat/body weight_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0005459I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal jaw morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000454I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal nasolacrimal duct morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0008969I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal limb long bone morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0011504I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal neuronal migration_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0006009I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• postnatal growth retardation_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0001732I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• decreased brain size_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000774I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal ear position_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000023I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal cortical plate morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0008439I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• decreased cerebral cortex pyramidal cell number_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0009974I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• decreased body weight_Kat6b<Gt(pKC199)1Pgr>/Kat6b<+>
  http://metadb.riken.jp/0001262I129Kat6bGtpKC1991PgrKat6bKat6bKat6bGtpKC1991Pgr
• abnormal long bone hypertrophic chondrocyte zone_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000165I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• microphthalmia_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0001297I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• small olfactory bulb_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0002741I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal muscle morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0002108I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal epiphyseal plate morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0006395I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr