abnormal skin morphology_Gjb2<tm2.2Kwi>/Gjb2<+>,Tg(Pgk1-cre)1Lni/0

http://metadb.riken.jp/0002060I129Sv129P2OlaHsdBALBcC57BL6Gjb2tm22KwiGjb2TgPgk1cre1Lni0Gjb2Gjb2tm22KwiTgPgk1cre1Lni

abnormal skin morphology_Gjb2<tm2.2Kwi>/Gjb2<+>,Tg(Pgk1-cre)1Lni/0

表現型アノテーション

MGI marker

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

• gap junction protein, beta 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:95720
• transgene insertion 1, Peter Lonai
  http://metadb.riken.jp/db/mgi_rdf/MGI:2178049

遺伝子型

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

• Gjb2<tm2.2Kwi>/Gjb2<+>,Tg(Pgk1-cre)1Lni/0

アレルシンボル

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

• Gjb2<+>|Gjb2<tm2.2Kwi>|Tg(Pgk1-cre)1Lni

遺伝的背景

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

• involves: 129/Sv * 129P2/OlaHsd * BALB/c * C57BL/6

MP annotation

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

• abnormal skin morphology
  http://purl.obolibrary.org/obo/MP_0002060

文献

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

• Melanie. Schütz, et.al., The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis-ichthyosis-deafness syndrome., Human molecular genetics, 2011, 20
  http://rdf.ncbi.nlm.nih.gov/pubmed/20926451