hindlimb paralysis_Dbnl<tm1Jwnd>/Dbnl<+>

http://metadb.riken.jp/0000755IBALBcDbnltm1JwndDbnlDbnlDbnltm1Jwnd

hindlimb paralysis_Dbnl<tm1Jwnd>/Dbnl<+>

表現型アノテーション

MGI marker

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

• drebrin-like
  http://metadb.riken.jp/db/mgi_rdf/MGI:700006

遺伝子型

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

• Dbnl<tm1Jwnd>/Dbnl<+>

アレルシンボル

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

• Dbnl<+>|Dbnl<tm1Jwnd>

遺伝的背景

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

• involves: BALB/c

MP annotation

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

• hindlimb paralysis
  http://purl.obolibrary.org/obo/MP_0000755

文献

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

• Sabine. Connert, et.al., SH3P7/mAbp1 deficiency leads to tissue and behavioral abnormalities and impaired vesicle transport., The EMBO journal, 2006, 25
  http://rdf.ncbi.nlm.nih.gov/pubmed/16601697