no abnormal phenotype detected_Crb2<tm1.1Wij>/Crb2<tm1.1Wij>

http://metadb.riken.jp/0002169I129P2OlaHsd129S4SvJaeSorCrb2tm11WijCrb2tm11WijCrb2tm11Wij

no abnormal phenotype detected_Crb2<tm1.1Wij>/Crb2<tm1.1Wij>

表現型アノテーション

MGI marker

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

• crumbs family member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2679260

遺伝子型

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

• Crb2<tm1.1Wij>/Crb2<tm1.1Wij>

アレルシンボル

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

• Crb2<tm1.1Wij>

遺伝的背景

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

• involves: 129P2/OlaHsd * 129S4/SvJaeSor

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

• Celso Henrique. Alves, et.al., Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene., Human molecular genetics, 2013, 22
  http://rdf.ncbi.nlm.nih.gov/pubmed/23001562