abnormal endocochlear potential_Ildr1<tm1(KOMP)Wtsi>/Ildr1<tm1(KOMP)Wtsi>

http://metadb.riken.jp/0002630IC57BL6NIldr1tm1KOMPWtsiIldr1tm1KOMPWtsiIldr1tm1KOMPWtsi

abnormal endocochlear potential_Ildr1<tm1(KOMP)Wtsi>/Ildr1<tm1(KOMP)Wtsi>

表現型アノテーション

MGI marker

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

• immunoglobulin-like domain containing receptor 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2146574

遺伝子型

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

• Ildr1<tm1(KOMP)Wtsi>/Ildr1<tm1(KOMP)Wtsi>

アレルシンボル

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

• Ildr1<tm1(KOMP)Wtsi>

遺伝的背景

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

• involves: C57BL/6N

MP annotation

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

• abnormal endocochlear potential
  http://purl.obolibrary.org/obo/MP_0002630

文献

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

• Eva L. Morozko, et.al., ILDR1 null mice, a model of human deafness DFNB42, show structural aberrations of tricellular tight junctions and degeneration of auditory hair cells., Human molecular genetics, 2015, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/25217574