hydroencephaly_Nfix<tm1Aes>/Nfix<tm1Aes>

http://metadb.riken.jp/0001891I129S1SvC57BL6Nfixtm1AesNfixtm1AesNfixtm1Aes

hydroencephaly_Nfix<tm1Aes>/Nfix<tm1Aes>

表現型アノテーション

MGI marker

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

• nuclear factor I/X
  http://metadb.riken.jp/db/mgi_rdf/MGI:97311

遺伝子型

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

• Nfix<tm1Aes>/Nfix<tm1Aes>

アレルシンボル

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

• Nfix<tm1Aes>

遺伝的背景

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

• involves: 129S1/Sv * C57BL/6

MP annotation

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

• hydroencephaly
  http://purl.obolibrary.org/obo/MP_0001891

文献

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

• Katrin. Driller, et.al., Nuclear factor I X deficiency causes brain malformation and severe skeletal defects., Molecular and cellular biology, 2007, 27
  http://rdf.ncbi.nlm.nih.gov/pubmed/17353270