no abnormal phenotype detected_Foxn1<tm1.1Dmsu>/Foxn1<tm1.1Dmsu>

http://metadb.riken.jp/0002169I129SvC57BL6SJLFoxn1tm11DmsuFoxn1tm11DmsuFoxn1tm11Dmsu

no abnormal phenotype detected_Foxn1<tm1.1Dmsu>/Foxn1<tm1.1Dmsu>

表現型アノテーション

MGI marker

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

• forkhead box N1
  http://metadb.riken.jp/db/mgi_rdf/MGI:102949

遺伝子型

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

• Foxn1<tm1.1Dmsu>/Foxn1<tm1.1Dmsu>

アレルシンボル

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

• Foxn1<tm1.1Dmsu>

遺伝的背景

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

• involves: 129/Sv * 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

• Lili. Cheng, et.al., Postnatal tissue-specific disruption of transcription factor FoxN1 triggers acute thymic atrophy., The Journal of biological chemistry, 2010, 285
  http://rdf.ncbi.nlm.nih.gov/pubmed/19955175