reduced enamel thickness_Gja1<tm8Kwi>/Gja1<+>,Tg(Pgk1-cre)1Lni/0

http://metadb.riken.jp/0002577I129S2SvPasBALBcC57BL6Gja1tm8KwiGja1TgPgk1cre1Lni0TgPgk1cre1LniGja1Gja1tm8Kwi

reduced enamel thickness_Gja1<tm8Kwi>/Gja1<+>,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

• transgene insertion 1, Peter Lonai
  http://metadb.riken.jp/db/mgi_rdf/MGI:2178049
• gap junction protein, alpha 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:95713

遺伝子型

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

• Gja1<tm8Kwi>/Gja1<+>,Tg(Pgk1-cre)1Lni/0

アレルシンボル

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

• Tg(Pgk1-cre)1Lni|Gja1<+>|Gja1<tm8Kwi>

遺伝的背景

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

• involves: 129S2/SvPas * BALB/c * C57BL/6

MP annotation

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

• reduced enamel thickness
  http://purl.obolibrary.org/obo/MP_0002577

文献

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

• Radoslaw. Dobrowolski, et.al., The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans., Human molecular genetics, 2008, 17
  http://rdf.ncbi.nlm.nih.gov/pubmed/18003637