organ of Corti degeneration_Pcdh15<av-Tg2742Rpw>/Pcdh15<av-Tg2742Rpw>

http://metadb.riken.jp/0000043FVBNPcdh15avTg2742RpwPcdh15avTg2742RpwPcdh15avTg2742RpwPcdh15avTg2742Rpw

organ of Corti degeneration_Pcdh15<av-Tg2742Rpw>/Pcdh15<av-Tg2742Rpw>

表現型アノテーション

MGI marker

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

• protocadherin 15
  http://metadb.riken.jp/db/mgi_rdf/MGI:1891428

遺伝子型

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

• Pcdh15<av-Tg2742Rpw>/Pcdh15<av-Tg2742Rpw>

アレルシンボル

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

• Pcdh15<av-Tg2742Rpw>

遺伝的背景

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

• FVB/N-Pcdh15<av-Tg2742Rpw>

MP annotation

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

• organ of Corti degeneration
  http://purl.obolibrary.org/obo/MP_0000043

文献

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

• K N. Alagramam, et.al., A new mouse insertional mutation that causes sensorineural deafness and vestibular defects., Genetics, 1999, 152
  http://rdf.ncbi.nlm.nih.gov/pubmed/10430593