abnormal motor capabilities/coordination/movement_Del(5Gtf2i-Fkbp6)1Vcam/+

http://metadb.riken.jp/0002066B6129Del5Gtf2iFkbp61VcamJ204278Del5Gtf2iFkbp61VcamDel5Gtf2iFkbp61Vcam

abnormal motor capabilities/coordination/movement_Del(5Gtf2i-Fkbp6)1Vcam/+

表現型アノテーション

MGI marker

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

• deletion, Chr5, Victoria Campuzano 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:5555957

遺伝子型

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

• Del(5Gtf2i-Fkbp6)1Vcam/+

アレルシンボル

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

• Del(5Gtf2i-Fkbp6)1Vcam|+

遺伝的背景

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

• B6.129-Del(5Gtf2i-Fkbp6)1Vcam(J:204278)

MP annotation

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

• abnormal motor capabilities/coordination/movement
  http://purl.obolibrary.org/obo/MP_0002066

文献

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

• Maria. Segura-Puimedon, et.al., Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder., Human molecular genetics, 2014, 23
  http://rdf.ncbi.nlm.nih.gov/pubmed/25027326