abnormal axon guidance_Ntn1<tm1.2Tek>/Ntn1<tm1.2Tek>

http://metadb.riken.jp/0002961I129S1Sv129X1SvJBALBcC57BL6SJLNtn1tm12TekNtn1tm12TekNtn1tm12Tek

abnormal axon guidance_Ntn1<tm1.2Tek>/Ntn1<tm1.2Tek>

表現型アノテーション

MGI marker

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

• netrin 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:105088

遺伝子型

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

• Ntn1<tm1.2Tek>/Ntn1<tm1.2Tek>

アレルシンボル

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

• Ntn1<tm1.2Tek>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * SJL

MP annotation

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

• abnormal axon guidance
  http://purl.obolibrary.org/obo/MP_0002961

文献

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

• Jenea M. Bin, et.al., Complete Loss of Netrin-1 Results in Embryonic Lethality and Severe Axon Guidance Defects without Increased Neural Cell Death., Cell reports, 2015, 12
  http://rdf.ncbi.nlm.nih.gov/pubmed/26257176