abnormal double-strand DNA break repair_Fancb<em1Shnk>/Fancb<em1Shnk>

http://metadb.riken.jp/0010948C57BL6JFancbem1ShnkFancbem1ShnkFancbem1ShnkFancbem1Shnk

abnormal double-strand DNA break repair_Fancb<em1Shnk>/Fancb<em1Shnk>

表現型アノテーション

MGI marker

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

• Fanconi anemia, complementation group B
  http://metadb.riken.jp/db/mgi_rdf/MGI:2448558

遺伝子型

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

• Fancb<em1Shnk>/Fancb<em1Shnk>

アレルシンボル

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

• Fancb<em1Shnk>

遺伝的背景

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

• C57BL/6J-Fancb<em1Shnk>

MP annotation

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

• abnormal double-strand DNA break repair
  http://purl.obolibrary.org/obo/MP_0010948

文献

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

• Yasuko. Kato, et.al., FANCB is essential in the male germline and regulates H3K9 methylation on the sex chromosomes during meiosis., Human molecular genetics, 2015, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/26123487