Dfnb59<tm1Ugds>

http://metadb.riken.jp/db/mgi_rdf/MGI:3654320

Dfnb59<tm1Ugds>

MGIアレル

synonym

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

アレルシンボル

http://www.w3.org/2000/01/rdf-schema#label

• Dfnb59<tm1Ugds>

MGI Accession ID

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

• MGI:3654320

Allele Name

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

• targeted mutation 1, Unite de Genetique des Deficits Sensoriels

Allele Type

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

• Targeted
  http://metadb.riken.jp/db/mgi_rdf/AlleleType/013

Allele Attribute

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

• Humanized sequence

PubMed ID for original reference

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

• Sedigheh. Delmaghani, et.al., Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy., Nature genetics, 2006, 38
  http://rdf.ncbi.nlm.nih.gov/pubmed/16804542

MGI marker

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

• deafness, autosomal recessive 59 (human)
  http://metadb.riken.jp/db/mgi_rdf/MGI:2685847

Mutant Cell Line IDs

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

See also (jump to original page)

http://www.w3.org/2000/01/rdf-schema#seeAlso

• http://identifiers.org/mgd/MGI:3654320

logical db name

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