no abnormal phenotype detected_Snrpn<tm3Alb>/Snrpn<+>

http://metadb.riken.jp/0002169EI129S7SvEvBrdorI129S7SvEvBrdC57BL6JSnrpntm3AlbSnrpnSnrpntm3AlbSnrpn

no abnormal phenotype detected_Snrpn<tm3Alb>/Snrpn<+>

表現型アノテーション

MGI marker

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

• small nuclear ribonucleoprotein N
  http://metadb.riken.jp/db/mgi_rdf/MGI:98347

遺伝子型

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

• Snrpn<tm3Alb>/Snrpn<+>

アレルシンボル

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

• Snrpn<tm3Alb>|Snrpn<+>

遺伝的背景

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

• either: (involves: 129S7/SvEvBrd) or (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