no abnormal phenotype detected_Tbx1<m1Jlk>/Tbx1<+>

http://metadb.riken.jp/0002169129SvTbx1m1JlkTbx1m1JlkTbx1Tbx1Tbx1m1Jlk

no abnormal phenotype detected_Tbx1<m1Jlk>/Tbx1<+>

表現型アノテーション

MGI marker

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

• T-box 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:98493

遺伝子型

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

• Tbx1<m1Jlk>/Tbx1<+>

アレルシンボル

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

• Tbx1<+>|Tbx1<m1Jlk>

遺伝的背景

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

• 129/Sv-Tbx1<m1Jlk>

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

• Murim. Choi, et.al., Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse., PLoS genetics, 2009, 5
  http://rdf.ncbi.nlm.nih.gov/pubmed/19247433