About: TP63 wt Allele     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • TP63 wt Allele
rdfs:subClassOf
OMIM_Number
  • 603273
GenBank_Accession_Number
  • AB010153
Semantic_Type
  • Gene or Genome
Preferred_Name
  • TP63 wt Allele
UMLS_CUI
  • C2984561
EntrezGene_ID
  • 8626
HGNC_ID
  • HGNC:15979
FULL_SYN
  • AISSYNCI
  • p40SYNCI
  • TP63 wt AllelePTNCI
  • P63SYNCI
  • p51SYNCI
  • p63SYNCI
  • NBPSYNCI
  • KETSYNCI
  • LMSSYNCI
  • RHSSYNCI
  • EEC3SYNCI
  • P73HSYNCI
  • P73LSYNCI
  • OFC8SYNCI
  • p73HSYNCI
  • p73LSYNCI
  • Tumor Protein p53-Like GeneSYNCI
  • Tumor Protein p73-Like GeneSYNCI
  • Tumor Protein p63 wt AlleleSYNCI
  • TP53LSYNCI
  • TP73LSYNCI
  • SHFM4SYNCI
  • p53CPSYNCI
  • TP53CPSYNCI
  • B(p51A)SYNCI
  • B(p51B)SYNCI
  • Tumor Protein p53-Competing Protein GeneSYNCI
DEFINITION
  • NCIHuman TP63 wild-type allele is located in the vicinity of 3q28 and is approximately 266 kb in length. This allele, which encodes tumor protein 63, is involved in the modulation of both apical ectoderm development and gene transcription. Mutation of the gene is associated with cervical, colon, head and neck, lung and ovarian cancers and numerous congenital disorders caused by aberrant ectodermal development and differentiation.
DesignNote
  • Mutation of the TP63 gene is associated with acro-dermato-ungual-lacrimal-tooth syndrome, ankyloblepharon-ectodermal defects-cleft lip/palate, ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome type 3, split-hand/foot malformation type 4, limb-mammary syndrome, ectodermal dysplasia Rapp-Hodgkin type and non-syndromic orofacial cleft type 8. (UniProt)
code
  • C91792
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