abnormal CNS synaptic transmission_Slc6a5<tm1Betz>/Slc6a5<tm1Betz>

http://metadb.riken.jp/0002206I129P2OlaHsdSlc6a5tm1BetzSlc6a5tm1BetzSlc6a5tm1Betz

abnormal CNS synaptic transmission_Slc6a5<tm1Betz>/Slc6a5<tm1Betz>

表現型アノテーション

MGI marker

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

• solute carrier family 6 (neurotransmitter transporter, glycine), member 5
  http://metadb.riken.jp/db/mgi_rdf/MGI:105090

遺伝子型

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

• Slc6a5<tm1Betz>/Slc6a5<tm1Betz>

アレルシンボル

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

• Slc6a5<tm1Betz>

遺伝的背景

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

• involves: 129P2/OlaHsd

MP annotation

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

• abnormal CNS synaptic transmission
  http://purl.obolibrary.org/obo/MP_0002206

文献

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

• Jesús. Gomeza, et.al., Deletion of the mouse glycine transporter 2 results in a hyperekplexia phenotype and postnatal lethality., Neuron, 2003, 40
  http://rdf.ncbi.nlm.nih.gov/pubmed/14622583