no abnormal phenotype detected_Igs13<tm1Dolm>/Igs13<+>,Igs14<tm1Dolm>/Igs14<+>

http://metadb.riken.jp/0002169I129P2OlaHsdC57BL6NIgs13tm1DolmIgs13Igs14tm1DolmIgs14Igs13tm1DolmIgs13Igs14tm1DolmIgs14

no abnormal phenotype detected_Igs13<tm1Dolm>/Igs13<+>,Igs14<tm1Dolm>/Igs14<+>

表現型アノテーション

MGI marker

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

• intergenic site 13
  http://metadb.riken.jp/db/mgi_rdf/MGI:5569494
• intergenic site 14
  http://metadb.riken.jp/db/mgi_rdf/MGI:5569495

遺伝子型

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

• Igs13<tm1Dolm>/Igs13<+>,Igs14<tm1Dolm>/Igs14<+>

アレルシンボル

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

• Igs13<tm1Dolm>|Igs13<+>|Igs14<tm1Dolm>|Igs14<+>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6N

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Thomas. Portmann, et.al., Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome., Cell reports, 2014, 7
  http://rdf.ncbi.nlm.nih.gov/pubmed/24794428