abnormal red nucleus morphology_Pou4f1<tm1Nat>/Pou4f1<tm1Nat>

http://metadb.riken.jp/0012267I129S7SvEvBrdC57BL6JPou4f1tm1NatPou4f1tm1NatPou4f1tm1Nat

abnormal red nucleus morphology_Pou4f1<tm1Nat>/Pou4f1<tm1Nat>

表現型アノテーション

MGI marker

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

• POU domain, class 4, transcription factor 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:102525

遺伝子型

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

• Pou4f1<tm1Nat>/Pou4f1<tm1Nat>

アレルシンボル

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

• Pou4f1<tm1Nat>

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

• abnormal red nucleus morphology
  http://purl.obolibrary.org/obo/MP_0012267

文献

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

• M. Xiang, et.al., Targeted deletion of the mouse POU domain gene Brn-3a causes selective loss of neurons in the brainstem and trigeminal ganglion, uncoordinated limb movement, and impaired suckling., Proceedings of the National Academy of Sciences of the United States of America, 1996, 93
  http://rdf.ncbi.nlm.nih.gov/pubmed/8876243