spleen hypoplasia_Nkx2-5<tm1Wehi>/Nkx2-5<+>

http://metadb.riken.jp/0000694I129P2OlaHsdNkx25tm1WehiNkx25Nkx25tm1WehiNkx25

spleen hypoplasia_Nkx2-5<tm1Wehi>/Nkx2-5<+>

表現型アノテーション

MGI marker

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

• NK2 homeobox 5
  http://metadb.riken.jp/db/mgi_rdf/MGI:97350

遺伝子型

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

• Nkx2-5<tm1Wehi>/Nkx2-5<+>

アレルシンボル

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

• Nkx2-5<tm1Wehi>|Nkx2-5<+>

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

• spleen hypoplasia
  http://purl.obolibrary.org/obo/MP_0000694

文献

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

• Matthew. Koss, et.al., Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module., Developmental cell, 2012, 22
  http://rdf.ncbi.nlm.nih.gov/pubmed/22560297