cochlear ganglion degeneration_Cacna1d<tm1Hssh>/Cacna1d<tm1Hssh>

http://metadb.riken.jp/0002857I129S4SvJaeC57BL6JCacna1dtm1HsshCacna1dtm1HsshCacna1dtm1Hssh

cochlear ganglion degeneration_Cacna1d<tm1Hssh>/Cacna1d<tm1Hssh>

表現型アノテーション

MGI marker

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

• calcium channel, voltage-dependent, L type, alpha 1D subunit
  http://metadb.riken.jp/db/mgi_rdf/MGI:88293

遺伝子型

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

• Cacna1d<tm1Hssh>/Cacna1d<tm1Hssh>

アレルシンボル

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

• Cacna1d<tm1Hssh>

遺伝的背景

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

• involves: 129S4/SvJae * C57BL/6J

MP annotation

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

• cochlear ganglion degeneration
  http://purl.obolibrary.org/obo/MP_0002857

文献

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

• Hongwei. Dou, et.al., Null mutation of alpha1D Ca2+ channel gene results in deafness but no vestibular defect in mice., Journal of the Association for Research in Otolaryngology : JARO, 2004, 5
  http://rdf.ncbi.nlm.nih.gov/pubmed/15357422