sensorineural hearing loss_Gjb6<tm1Kwi>/Gjb6<tm1Kwi>

http://metadb.riken.jp/0004740I129P2OlaHsdC57BL6Gjb6tm1KwiGjb6tm1KwiGjb6tm1Kwi

sensorineural hearing loss_Gjb6<tm1Kwi>/Gjb6<tm1Kwi>

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<tm1Kwi>/Gjb6<tm1Kwi>

アレルシンボル

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

• Gjb6<tm1Kwi>

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

• sensorineural hearing loss
  http://purl.obolibrary.org/obo/MP_0004740

文献

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

• Barbara. Teubner, et.al., Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential., Human molecular genetics, 2003, 12
  http://rdf.ncbi.nlm.nih.gov/pubmed/12490528