K(lysine) acetyltransferase 6B

http://metadb.riken.jp/db/mgi_rdf/MGI:1858746

K(lysine) acetyltransferase 6B

marker

発現マップ

http://vibrism.neuroinf.jp/dev/201509/rdf/mgiGene

• ExpressionMap(C57BL/6J,8week,male):Cx132788
  http://vibrism.neuroinf.jp/dev/201509/rdf/ExpressionMap/C57BL_6J_8week_male/Cx132788
• ExpressionMap(C57BL/6J,3week,male):Cg008175
  http://vibrism.neuroinf.jp/dev/201509/rdf/ExpressionMap/C57BL_6J_3week_male/Cg008175
• ExpressionMap(C57BL/6J,8week,male):Cx133674
  http://vibrism.neuroinf.jp/dev/201509/rdf/ExpressionMap/C57BL_6J_8week_male/Cx133674
• ExpressionMap(C57BL/6J,8week,male):Cx105744
  http://vibrism.neuroinf.jp/dev/201509/rdf/ExpressionMap/C57BL_6J_8week_male/Cx105744
• ExpressionMap(C57BL/6J,3day,male):Ce024254
  http://vibrism.neuroinf.jp/dev/201509/rdf/ExpressionMap/C57BL_6J_3day_male/Ce024254
• ExpressionMap(C57BL/6J,7day,male):Cf011811
  http://vibrism.neuroinf.jp/dev/201509/rdf/ExpressionMap/C57BL_6J_7day_male/Cf011811
• ExpressionMap(C57BL/6J,3day,male):Ce011139
  http://vibrism.neuroinf.jp/dev/201509/rdf/ExpressionMap/C57BL_6J_3day_male/Ce011139
• ExpressionMap(C57BL/6J,7day,male):Cf026323
  http://vibrism.neuroinf.jp/dev/201509/rdf/ExpressionMap/C57BL_6J_7day_male/Cf026323
• ExpressionMap(C57BL/6J,3week,male):Cg008174
  http://vibrism.neuroinf.jp/dev/201509/rdf/ExpressionMap/C57BL_6J_3week_male/Cg008174

シノニム

http://metadb.riken.jp/db/mgi_rdf/Marker_Synonyms

genetic mapping procedure

http://metadb.riken.jp/db/mgi_rdf/genetic_mapping_procedure

シンボル

http://metadb.riken.jp/db/mgi_rdf/Marker_Symbol

Marker Type

http://metadb.riken.jp/db/mgi_rdf/Marker_Type

Feature Type

http://metadb.riken.jp/db/mgi_rdf/Feature_Type

Status

http://metadb.riken.jp/db/mgi_rdf/Status

genome coordinate start

http://metadb.riken.jp/db/mgi_rdf/genome_coordinate_start

See also (jump to original page)

http://www.w3.org/2000/01/rdf-schema#seeAlso

染色体

http://metadb.riken.jp/db/mgi_rdf/MouseChromosome

genome coordinate end

http://metadb.riken.jp/db/mgi_rdf/genome_coordinate_end

strand

http://metadb.riken.jp/db/mgi_rdf/strand

位置（遺伝的距離）

http://metadb.riken.jp/db/mgi_rdf/cM_Position

MGI Accession ID

http://metadb.riken.jp/db/mgi_rdf/MGI_ID

トランスクリプトームデータ

http://metadb.riken.jp/db/BrainTx/mgiGene

• CD20116
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD20116

allele

http://metadb.riken.jp/db/mgi_rdf/variant_of

• Kat6b<m1Mhda>
  http://metadb.riken.jp/db/mgi_rdf/MGI:5702933
• Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2679726

表現型アノテーション

http://metadb.riken.jp/db/mgi_rdf/variant_of

• abnormal occipital bone morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0005269I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal coronal suture morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0003840I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal muscle morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0002108I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• decreased inferior colliculus size_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0009038I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal cerebral cortex morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000788I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• postnatal growth retardation_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0001732I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• microphthalmia_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0001297I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal ear position_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000023I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• decreased brain size_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000774I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal neuronal migration_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0006009I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal nasolacrimal duct morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0008969I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• decreased body weight_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0001262I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal jaw morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000454I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• shortened head_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000435I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• decreased body size_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0001265I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• decreased cerebral cortex pyramidal cell number_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0009974I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal long bone hypertrophic chondrocyte zone_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000165I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal limb long bone morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0011504I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• decreased body weight_Kat6b<Gt(pKC199)1Pgr>/Kat6b<+>
  http://metadb.riken.jp/0001262I129Kat6bGtpKC1991PgrKat6bKat6bKat6bGtpKC1991Pgr
• small olfactory bulb_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0002741I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal parietal bone morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000109I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal epiphyseal plate morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0006395I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal cranium morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000438I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• decreased percent body fat/body weight_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0005459I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• no abnormal phenotype detected_Kat6b<m1Mhda>/Kat6b<+>
  http://metadb.riken.jp/0002169C3HeBFeJKat6bm1MhdaKat6bm1MhdaKat6bKat6bKat6bm1Mhda
• abnormal telencephalon development_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0000934I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• abnormal cortical plate morphology_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0008439I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• postnatal lethality, incomplete penetrance_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0011086I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr
• prenatal lethality, complete penetrance_Kat6b<m1Mhda>/Kat6b<m1Mhda>
  http://metadb.riken.jp/0011091C3HeBFeJKat6bm1MhdaKat6bm1MhdaKat6bm1MhdaKat6bm1Mhda
• delayed suture closure_Kat6b<Gt(pKC199)1Pgr>/Kat6b<Gt(pKC199)1Pgr>
  http://metadb.riken.jp/0010743I129Kat6bGtpKC1991PgrKat6bGtpKC1991PgrKat6bGtpKC1991Pgr

MouseAllele

http://metadb.riken.jp/db/bioresource_schema/brs_variantOf

• gene trap NAISTrap_1TP-137, Yasumasa Ishida
  http://metadb.riken.jp/db/rikenbrc_mouse/brc_allele1561