About: MID1 wt Allele     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • MID1 wt Allele
rdfs:subClassOf
OMIM_Number
  • 300552
GenBank_Accession_Number
  • Y13667
Semantic_Type
  • Gene or Genome
Preferred_Name
  • MID1 wt Allele
UMLS_CUI
  • C2697964
EntrezGene_ID
  • 4281
Legacy_Concept_Name
  • MID1_wt_Allele
HGNC_ID
  • HGNC:7095
FULL_SYN
  • MID1 wt AllelePTNCI
  • OSSYNCI
  • FXYSYNCI
  • OSXSYNCI
  • OGS1SYNCI
  • XPRFSYNCI
  • BBBG1SYNCI
  • GBBB1SYNCI
  • RNF59SYNCI
  • MIDINSYNCI
  • ZNFXYSYNCI
  • TRIM18SYNCI
  • Midline 1 (Opitz/BBB Syndrome) wt AlleleSYNCI
DEFINITION
  • Human MID1 wild-type allele is located in the vicinity of Xp22 and is approximately 388 kb in length. This allele, which encodes midline-1 protein, plays a role in the modulation of microtubule organization. Mutations in this gene may be associated with the X-linked form of Opitz syndrome.NCI
code
  • C75731
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