no abnormal phenotype detected_Kat2b<tm1Roth>/Kat2b<tm1Roth>

http://metadb.riken.jp/0002169I129S7SvEvBrdC57BL6JKat2btm1RothKat2btm1RothKat2btm1Roth

no abnormal phenotype detected_Kat2b<tm1Roth>/Kat2b<tm1Roth>

表現型アノテーション

MGI marker

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

• K(lysine) acetyltransferase 2B
  http://metadb.riken.jp/db/mgi_rdf/MGI:1343094

遺伝子型

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

• Kat2b<tm1Roth>/Kat2b<tm1Roth>

アレルシンボル

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

• Kat2b<tm1Roth>

遺伝的背景

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

• involves: 129S7/SvEvBrd * C57BL/6J

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

• W. Xu, et.al., Loss of Gcn5l2 leads to increased apoptosis and mesodermal defects during mouse development., Nature genetics, 2000, 26
  http://rdf.ncbi.nlm.nih.gov/pubmed/11017084