no abnormal phenotype detected_Snord116<tm1Uta>/Snord116<tm1Uta>

http://metadb.riken.jp/0002169IC57BL6JSnord116tm1UtaSnord116tm1UtaSnord116tm1Uta

no abnormal phenotype detected_Snord116<tm1Uta>/Snord116<tm1Uta>

表現型アノテーション

MGI marker

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

• small nucleolar RNA, C/D box 116 cluster
  http://metadb.riken.jp/db/mgi_rdf/MGI:1891407

遺伝子型

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

• Snord116<tm1Uta>/Snord116<tm1Uta>

アレルシンボル

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

• Snord116<tm1Uta>

遺伝的背景

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

• involves: 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

• Feng. Ding, et.al., SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice., PloS one, 2008, 3
  http://rdf.ncbi.nlm.nih.gov/pubmed/18320030