abnormal myelination_Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>

http://metadb.riken.jp/0000920I129P2OlaHsdC57BL6Gjc2tm1EGFPKwiGjc2tm1EGFPKwiGjc2tm1EGFPKwi

abnormal myelination_Gjc2<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>

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<tm1(EGFP)Kwi>/Gjc2<tm1(EGFP)Kwi>

アレルシンボル

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

• Gjc2<tm1(EGFP)Kwi>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

MP annotation

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

• abnormal myelination
  http://purl.obolibrary.org/obo/MP_0000920

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
• Benjamin. Odermatt, et.al., Connexin 47 (Cx47)-deficient mice with enhanced green fluorescent protein reporter gene reveal predominant oligodendrocytic expression of Cx47 and display vacuolized myelin in the CNS., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2003, 23
  http://rdf.ncbi.nlm.nih.gov/pubmed/12805295