abnormal cochlear potential_Gjb6<tm1.1Fama>/Gjb6<tm1.1Fama>

http://metadb.riken.jp/0006332I129P2OlaHsdC57BL6SJLGjb6tm11FamaGjb6tm11FamaGjb6tm11Fama

abnormal cochlear potential_Gjb6<tm1.1Fama>/Gjb6<tm1.1Fama>

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 6
  http://metadb.riken.jp/db/mgi_rdf/MGI:107588

遺伝子型

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

• Gjb6<tm1.1Fama>/Gjb6<tm1.1Fama>

アレルシンボル

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

• Gjb6<tm1.1Fama>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6 * SJL

MP annotation

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

• abnormal cochlear potential
  http://purl.obolibrary.org/obo/MP_0006332

文献

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

• Melanie. Schütz, et.al., The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice., Human molecular genetics, 2010, 19
  http://rdf.ncbi.nlm.nih.gov/pubmed/20858605