no abnormal phenotype detected_Igs8<tm1Jw>/Igs8<+>

http://metadb.riken.jp/0002169NSIgs8tm1JwIgs8Igs8tm1JwIgs8

no abnormal phenotype detected_Igs8<tm1Jw>/Igs8<+>

表現型アノテーション

MGI marker

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

• intergenic site 8
  http://metadb.riken.jp/db/mgi_rdf/MGI:5503046

遺伝子型

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

• Igs8<tm1Jw>/Igs8<+>

アレルシンボル

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

• Igs8<tm1Jw>|Igs8<+>

遺伝的背景

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

• Not Specified

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

• Jian. Zhou, et.al., Respiratory failure, cleft palate and epilepsy in the mouse model of human Xq22.1 deletion syndrome., Human molecular genetics, 2014, 23
  http://rdf.ncbi.nlm.nih.gov/pubmed/24569167