abnormal chromosomal synapsis_Meikin<tm1Yow>/Meikin<tm1Yow>

http://metadb.riken.jp/0009451IC57BL6Meikintm1YowMeikintm1YowMeikintm1Yow

abnormal chromosomal synapsis_Meikin<tm1Yow>/Meikin<tm1Yow>

表現型アノテーション

MGI marker

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

• meiotic kinetochore factor
  http://metadb.riken.jp/db/mgi_rdf/MGI:1922097

遺伝子型

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

• Meikin<tm1Yow>/Meikin<tm1Yow>

アレルシンボル

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

• Meikin<tm1Yow>

遺伝的背景

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

• involves: C57BL/6

MP annotation

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

• abnormal chromosome pairing during meiosis
  http://purl.obolibrary.org/obo/MP_0009451

文献

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

• Jihye. Kim, et.al., Meikin is a conserved regulator of meiosis-I-specific kinetochore function., Nature, 2015, 517
  http://rdf.ncbi.nlm.nih.gov/pubmed/25533956