no abnormal phenotype detected_Hip1<tm2Tsr>/Hip1<tm2Tsr>

http://metadb.riken.jp/0002169I129X1SvJC57BL6Hip1tm2TsrHip1tm2TsrHip1tm2Tsr

no abnormal phenotype detected_Hip1<tm2Tsr>/Hip1<tm2Tsr>

表現型アノテーション

MGI marker

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

• huntingtin interacting protein 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1099804

遺伝子型

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

• Hip1<tm2Tsr>/Hip1<tm2Tsr>

アレルシンボル

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

• Hip1<tm2Tsr>

遺伝的背景

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

• involves: 129X1/SvJ * C57BL/6

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

• Katherine I. Oravecz-Wilson, et.al., Huntingtin Interacting Protein 1 mutations lead to abnormal hematopoiesis, spinal defects and cataracts., Human molecular genetics, 2004, 13
  http://rdf.ncbi.nlm.nih.gov/pubmed/14998932