no abnormal phenotype detected_Kmt2b<tm1.1Afst>/Kmt2b<tm1.1Afst>

http://metadb.riken.jp/0002169I129P2OlaHsdC57BL6SJLKmt2btm11AfstKmt2btm11AfstKmt2btm11Afst

no abnormal phenotype detected_Kmt2b<tm1.1Afst>/Kmt2b<tm1.1Afst>

表現型アノテーション

MGI marker

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

• lysine (K)-specific methyltransferase 2B
  http://metadb.riken.jp/db/mgi_rdf/MGI:109565

遺伝子型

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

• Kmt2b<tm1.1Afst>/Kmt2b<tm1.1Afst>

アレルシンボル

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

• Kmt2b<tm1.1Afst>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6 * SJL

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Stefan. Glaser, et.al., Multiple epigenetic maintenance factors implicated by the loss of Mll2 in mouse development., Development (Cambridge, England), 2006, 133
  http://rdf.ncbi.nlm.nih.gov/pubmed/16540515