hypoactivity_Gjc2<tm2.1Kwi>/Gjc2<+>

http://metadb.riken.jp/0001402IC57BL6SJLGjc2tm21KwiGjc2Gjc2tm21KwiGjc2

hypoactivity_Gjc2<tm2.1Kwi>/Gjc2<+>

表現型アノテーション

MGI marker

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

• gap junction protein, gamma 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2153060

遺伝子型

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

• Gjc2<tm2.1Kwi>/Gjc2<+>

アレルシンボル

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

• Gjc2<tm2.1Kwi>|Gjc2<+>

遺伝的背景

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

• involves: C57BL/6 * SJL

MP annotation

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

• hypoactivity
  http://purl.obolibrary.org/obo/MP_0001402

文献

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

• Oliver. Tress, et.al., Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes Pelizaeus-Merzbacher-like disease in humans., PLoS genetics, 2011, 7
  http://rdf.ncbi.nlm.nih.gov/pubmed/21750683