no abnormal phenotype detected_Epn2<tm1Ocr>/Epn2<tm1Ocr>

http://metadb.riken.jp/0002169B6129X1Epn2tm1OcrEpn2tm1OcrEpn2tm1OcrEpn2tm1Ocr

no abnormal phenotype detected_Epn2<tm1Ocr>/Epn2<tm1Ocr>

表現型アノテーション

MGI marker

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

• epsin 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1333766

遺伝子型

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

• Epn2<tm1Ocr>/Epn2<tm1Ocr>

アレルシンボル

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

• Epn2<tm1Ocr>

遺伝的背景

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

• B6.129X1-Epn2<tm1Ocr>

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

• Hong. Chen, et.al., Embryonic arrest at midgestation and disruption of Notch signaling produced by the absence of both epsin 1 and epsin 2 in mice., Proceedings of the National Academy of Sciences of the United States of America, 2009, 106
  http://rdf.ncbi.nlm.nih.gov/pubmed/19666558