abnormal embryo development_Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?

http://metadb.riken.jp/0001672I129S7SvEvBrdC57BL6FVBNArhgap6HccsMid1tm1HzoArhgap6HccsMid1tm1HzoTgEIIacreC5379LmgdArhgap6HccsMid1tm1HzoTgEIIacreC5379Lmgd

abnormal embryo development_Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?

表現型アノテーション

MGI marker

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

• transgene insertion C5379, Laboratory of Mammalian Genes and Development, Heiner Westphal
  http://metadb.riken.jp/db/mgi_rdf/MGI:2137685
• holocytochrome c synthetase
  http://metadb.riken.jp/db/mgi_rdf/MGI:106911

遺伝子型

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

• Arhgap6/Hccs/Mid1<tm1Hzo>/Arhgap6/Hccs/Mid1<tm1Hzo>,Tg(EIIa-cre)C5379Lmgd/?

アレルシンボル

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

• Arhgap6/Hccs/Mid1<tm1Hzo>|Tg(EIIa-cre)C5379Lmgd

遺伝的背景

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

• involves: 129S7/SvEvBrd * C57BL/6 * FVB/N

MP annotation

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

• abnormal embryogenesis/ development
  http://purl.obolibrary.org/obo/MP_0001672

文献

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

• Siddharth K. Prakash, et.al., Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome., Human molecular genetics, 2002, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/12444108