no abnormal phenotype detected_Del(7Ube3a-Snrpn)1Alb/+

http://metadb.riken.jp/0002169I129S7SvEvBrdC57BL6JDel7Ube3aSnrpn1AlbDel7Ube3aSnrpn1Alb

no abnormal phenotype detected_Del(7Ube3a-Snrpn)1Alb/+

表現型アノテーション

MGI marker

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

• Deletion, Chr 7, Beaudet 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:3655807

遺伝子型

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

• Del(7Ube3a-Snrpn)1Alb/+

アレルシンボル

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

• +|Del(7Ube3a-Snrpn)1Alb

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• T F. Tsai, et.al., Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome., Human molecular genetics, 1999, 8
  http://rdf.ncbi.nlm.nih.gov/pubmed/10400982