abnormal gait_Kat2a<tm3.1Roth>/Kat2a<tm3.2Roth>,Tg(Pcp2-cre)2Mpin/0

http://metadb.riken.jp/0001406I129Kat2atm31RothKat2atm32RothTgPcp2cre2Mpin0TgPcp2cre2MpinKat2atm32RothKat2atm31Roth

abnormal gait_Kat2a<tm3.1Roth>/Kat2a<tm3.2Roth>,Tg(Pcp2-cre)2Mpin/0

表現型アノテーション

MGI marker

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

• transgene insertion 2, Max-Planck-Institute of Neurobiology
  http://metadb.riken.jp/db/mgi_rdf/MGI:2137514
• K(lysine) acetyltransferase 2A
  http://metadb.riken.jp/db/mgi_rdf/MGI:1343101

遺伝子型

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

• Kat2a<tm3.1Roth>/Kat2a<tm3.2Roth>,Tg(Pcp2-cre)2Mpin/0

アレルシンボル

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

• Tg(Pcp2-cre)2Mpin|Kat2a<tm3.2Roth>|Kat2a<tm3.1Roth>

遺伝的背景

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

• involves: 129

MP annotation

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

• abnormal gait
  http://purl.obolibrary.org/obo/MP_0001406

文献

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

• Yi Chun. Chen, et.al., Gcn5 loss-of-function accelerates cerebellar and retinal degeneration in a SCA7 mouse model., Human molecular genetics, 2012, 21
  http://rdf.ncbi.nlm.nih.gov/pubmed/22002997