corneal-lenticular stalk_Caprin2<tm2a(EUCOMM)Wtsi>/Caprin2<tm2a(EUCOMM)Wtsi>,Tg(Pax6-GFP/cre)1Rilm/0

http://metadb.riken.jp/0010713IC57BL6JC57BL6NTacFVBNCaprin2tm2aEUCOMMWtsiCaprin2tm2aEUCOMMWtsiTgPax6GFPcre1Rilm0Caprin2tm2aEUCOMMWtsiTgPax6GFPcre1Rilm

corneal-lenticular stalk_Caprin2<tm2a(EUCOMM)Wtsi>/Caprin2<tm2a(EUCOMM)Wtsi>,Tg(Pax6-GFP/cre)1Rilm/0

表現型アノテーション

MGI marker

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

• caprin family member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2448541
• transgene insertion 1, Richard L Maas
  http://metadb.riken.jp/db/mgi_rdf/MGI:5538354

遺伝子型

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

• Caprin2<tm2a(EUCOMM)Wtsi>/Caprin2<tm2a(EUCOMM)Wtsi>,Tg(Pax6-GFP/cre)1Rilm/0

アレルシンボル

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

• Caprin2<tm2a(EUCOMM)Wtsi>|Tg(Pax6-GFP/cre)1Rilm

遺伝的背景

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

• involves: C57BL/6J * C57BL/6NTac * FVB/N

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• corneal-lenticular stalk
  http://purl.obolibrary.org/obo/MP_0010713

文献

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

• Soma. Dash, et.al., Deficiency of the RNA binding protein caprin2 causes lens defects and features of Peters anomaly., Developmental dynamics : an official publication of the American Association of Anatomists, 2015, 244
  http://rdf.ncbi.nlm.nih.gov/pubmed/26177727