no abnormal phenotype detected_Tbx22<tm1Sta>/Y

http://metadb.riken.jp/0002169NSTbx22tm1StaYTbx22tm1Sta

no abnormal phenotype detected_Tbx22<tm1Sta>/Y

表現型アノテーション

MGI marker

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

• T-box 22
  http://metadb.riken.jp/db/mgi_rdf/MGI:2389465

遺伝子型

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

• Tbx22<tm1Sta>/Y

アレルシンボル

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

• Tbx22<tm1Sta>

遺伝的背景

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

• Not Specified

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

• Erwin. Pauws, et.al., Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes., Human molecular genetics, 2009, 18
  http://rdf.ncbi.nlm.nih.gov/pubmed/19648291