no abnormal phenotype detected_Arhgap6/Hccs/Mid1<tm1Hzo>/Y

http://metadb.riken.jp/0002169I129S7SvEvBrdArhgap6HccsMid1tm1HzoYArhgap6HccsMid1tm1Hzo

no abnormal phenotype detected_Arhgap6/Hccs/Mid1<tm1Hzo>/Y

表現型アノテーション

MGI marker

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

• holocytochrome c synthetase
  http://metadb.riken.jp/db/mgi_rdf/MGI:106911
• midline 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1100537
• Rho GTPase activating protein 6
  http://metadb.riken.jp/db/mgi_rdf/MGI:1196332

遺伝子型

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

• Arhgap6/Hccs/Mid1<tm1Hzo>/Y

アレルシンボル

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

• Arhgap6/Hccs/Mid1<tm1Hzo>

遺伝的背景

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

• involves: 129S7/SvEvBrd

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

• 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