hyperpigmentation_Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>

http://metadb.riken.jp/0001188I129Sv129S6SvEvTacC57BL6SJLPot1btm11SchgPot1btm11SchgPot1btm11Schg

hyperpigmentation_Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>

表現型アノテーション

MGI marker

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

• protection of telomeres 1B
  http://metadb.riken.jp/db/mgi_rdf/MGI:1920086

遺伝子型

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

• Pot1b<tm1.1Schg>/Pot1b<tm1.1Schg>

アレルシンボル

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

• Pot1b<tm1.1Schg>

遺伝的背景

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

• involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL

MP annotation

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

• hyperpigmentation
  http://purl.obolibrary.org/obo/MP_0001188

文献

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

• Hua. He, et.al., Pot1b deletion and telomerase haploinsufficiency in mice initiate an ATR-dependent DNA damage response and elicit phenotypes resembling dyskeratosis congenita., Molecular and cellular biology, 2009, 29
  http://rdf.ncbi.nlm.nih.gov/pubmed/18936156