abnormal axon guidance_Nr2f1<tm1Mjts>/Nr2f1<tm1Mjts>

http://metadb.riken.jp/0002961I129S7SvEvBrdC57BL6Nr2f1tm1MjtsNr2f1tm1MjtsNr2f1tm1Mjts

abnormal axon guidance_Nr2f1<tm1Mjts>/Nr2f1<tm1Mjts>

表現型アノテーション

MGI marker

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

• nuclear receptor subfamily 2, group F, member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1352451

遺伝子型

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

• Nr2f1<tm1Mjts>/Nr2f1<tm1Mjts>

アレルシンボル

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

• Nr2f1<tm1Mjts>

遺伝的背景

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

• involves: 129S7/SvEvBrd * C57BL/6

MP annotation

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

• abnormal axon guidance
  http://purl.obolibrary.org/obo/MP_0002961

文献

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

• Y. Qiu, et.al., Null mutation of mCOUP-TFI results in defects in morphogenesis of the glossopharyngeal ganglion, axonal projection, and arborization., Genes & development, 1997, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/9271116