no abnormal phenotype detected_Del(XNxf2-Tmsb15a)2Jw/Y

http://metadb.riken.jp/0002169I129S4SvJaeC57BL6FVBDelXNxf2Tmsb15a2JwYDelXNxf2Tmsb15a2Jw

no abnormal phenotype detected_Del(XNxf2-Tmsb15a)2Jw/Y

表現型アノテーション

MGI marker

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

• deletion, Chr X, Jeremy Wang 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:5584167

遺伝子型

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

• Del(XNxf2-Tmsb15a)2Jw/Y

アレルシンボル

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

• Del(XNxf2-Tmsb15a)2Jw

遺伝的背景

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

• involves: 129S4/SvJae * C57BL/6 * FVB

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

• Jian. Zhou, et.al., Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome., Human molecular genetics, 2014, 23
  http://rdf.ncbi.nlm.nih.gov/pubmed/24569167