alopecia_Ctnnb1<tm4Wbm>/Ctnnb1<+>,Tg(KRT14-cre)1Efu/0

http://metadb.riken.jp/0000414I129P2OlaHsdCtnnb1tm4WbmCtnnb1TgKRT14cre1Efu0Ctnnb1tm4WbmCtnnb1TgKRT14cre1Efu

alopecia_Ctnnb1<tm4Wbm>/Ctnnb1<+>,Tg(KRT14-cre)1Efu/0

表現型アノテーション

MGI marker

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

• transgene insertion 1, Elaine Fuchs
  http://metadb.riken.jp/db/mgi_rdf/MGI:1926453
• catenin (cadherin associated protein), beta 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:88276

遺伝子型

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

• Ctnnb1<tm4Wbm>/Ctnnb1<+>,Tg(KRT14-cre)1Efu/0

アレルシンボル

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

• Ctnnb1<tm4Wbm>|Ctnnb1<+>|Tg(KRT14-cre)1Efu

遺伝的背景

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

• involves: 129P2/OlaHsd

MP annotation

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

• alopecia
  http://purl.obolibrary.org/obo/MP_0000414

文献

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

• Wei. Liu, et.al., Deletion of Porcn in mice leads to multiple developmental defects and models human focal dermal hypoplasia (Goltz syndrome)., PloS one, 2012, 7
  http://rdf.ncbi.nlm.nih.gov/pubmed/22412863