abnormal rod electrophysiology_Spata7<tm1Mrd>/Spata7<tm1Mrd>

http://metadb.riken.jp/0004021I129S7SvEvBrdSpata7tm1MrdSpata7tm1MrdSpata7tm1Mrd

abnormal rod electrophysiology_Spata7<tm1Mrd>/Spata7<tm1Mrd>

表現型アノテーション

MGI marker

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

• spermatogenesis associated 7
  http://metadb.riken.jp/db/mgi_rdf/MGI:2144877

遺伝子型

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

• Spata7<tm1Mrd>/Spata7<tm1Mrd>

アレルシンボル

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

• Spata7<tm1Mrd>

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

• abnormal rod electrophysiology
  http://purl.obolibrary.org/obo/MP_0004021

文献

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

• Aiden. Eblimit, et.al., Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina., Human molecular genetics, 2015, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/25398945