no abnormal phenotype detected_Nefl<tm1.1Liem>/Nefl<tm1.1Liem>

http://metadb.riken.jp/0002169B6CgNefltm11LiemNefltm11LiemNefltm11LiemNefltm11Liem

no abnormal phenotype detected_Nefl<tm1.1Liem>/Nefl<tm1.1Liem>

表現型アノテーション

MGI marker

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

• neurofilament, light polypeptide
  http://metadb.riken.jp/db/mgi_rdf/MGI:97313

遺伝子型

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

• Nefl<tm1.1Liem>/Nefl<tm1.1Liem>

アレルシンボル

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

• Nefl<tm1.1Liem>

遺伝的背景

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

• B6.Cg-Nefl<tm1.1Liem>

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

• Adijat A. Adebola, et.al., Neurofilament light polypeptide gene N98S mutation in mice leads to neurofilament network abnormalities and a Charcot-Marie-Tooth Type 2E phenotype., Human molecular genetics, 2015, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/25552649