no abnormal phenotype detected_Snrpn<tm1Cbr>/Snrpn<tm1Cbr>

http://metadb.riken.jp/0002169I129S1SvC57BL6Snrpntm1CbrSnrpntm1CbrSnrpntm1Cbr

no abnormal phenotype detected_Snrpn<tm1Cbr>/Snrpn<tm1Cbr>

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<tm1Cbr>/Snrpn<tm1Cbr>

アレルシンボル

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

• Snrpn<tm1Cbr>

遺伝的背景

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

• involves: 129S1/Sv * C57BL/6

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. Yang, et.al., A mouse model for Prader-Willi syndrome imprinting-centre mutations., Nature genetics, 1998, 19
  http://rdf.ncbi.nlm.nih.gov/pubmed/9590284