decreased cochlear microphonics_Pdzd7<tm1a(EUCOMM)Wtsi>/Pdzd7<tm1a(EUCOMM)Wtsi>

http://metadb.riken.jp/0004414IC57BL6JC57BL6NPdzd7tm1aEUCOMMWtsiPdzd7tm1aEUCOMMWtsiPdzd7tm1aEUCOMMWtsi

decreased cochlear microphonics_Pdzd7<tm1a(EUCOMM)Wtsi>/Pdzd7<tm1a(EUCOMM)Wtsi>

表現型アノテーション

MGI marker

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

• PDZ domain containing 7
  http://metadb.riken.jp/db/mgi_rdf/MGI:3608325

遺伝子型

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

• Pdzd7<tm1a(EUCOMM)Wtsi>/Pdzd7<tm1a(EUCOMM)Wtsi>

アレルシンボル

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

• Pdzd7<tm1a(EUCOMM)Wtsi>

遺伝的背景

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

• involves: C57BL/6J * C57BL/6N

MP annotation

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

• decreased cochlear microphonics
  http://purl.obolibrary.org/obo/MP_0004414

文献

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

• Junhuang. Zou, et.al., Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in mice., Human molecular genetics, 2014, 23
  http://rdf.ncbi.nlm.nih.gov/pubmed/24334608