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Details
Link-It Detail - Disease - Allelic Imbalance
Debug Stats
  • ### Total Build Time: 35 ms 21.420 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 253 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=2 ms Completed: 2 ms rowSize= 198 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=21 ms Completed: 21 ms rowSize= 19.344 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Allelic Imbalance C0887935
Definition (1)
A situation where one member (allele) of a gene pair is lost (LOSS OF HETEROZYGOSITY) or amplified.
Semantic Types (1)
Cell or Molecular Dysfunction (T049)
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanRASEF158158RAS and EF-hand domain containing
img GENERIF, Score=1000, Pubmed Id: 18385040, UMLKSK CUI: C0887935
HumanNIT256954nitrilase family, member 2
img GENERIF, Score=673, Pubmed Id: 17488281, UMLKSK CUI: C0887935
HumanC11orf3056946chromosome 11 open reading frame 30
img GENERIF, Score=901, Pubmed Id: 18787380, UMLKSK CUI: C0887935
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
img GENERIF, Score=1000, Pubmed Id: 18279374, UMLKSK CUI: C0887935
HumanTP537157tumor protein p53
img GENERIF, Score=1000, Pubmed Id: 18094375, UMLKSK CUI: C0887935
img GENERIF, Score=1000, Pubmed Id: 16273227, UMLKSK CUI: C0887935
HumanPLAGL15325pleiomorphic adenoma gene-like 1
img GENERIF, Score=1000, Pubmed Id: 16733217, UMLKSK CUI: C0887935
HumanABCB15243ATP-binding cassette, sub-family B (MDR/TAP), member 1
img GENERIF, Score=660, Pubmed Id: 18075465, UMLKSK CUI: C0887935
HumanMMP14312matrix metallopeptidase 1 (interstitial collagenase)
img GENERIF, Score=913, Pubmed Id: 15638833, UMLKSK CUI: C0887935
HumanSMAD44089SMAD family member 4
img GENERIF, Score=901, Pubmed Id: 15814640, UMLKSK CUI: C0887935
HumanERBB22064v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2
img GENERIF, Score=1000, Pubmed Id: 18854030, UMLKSK CUI: C0887935
HumanEGFR1956epidermal growth factor receptor
img GENERIF, Score=1000, Pubmed Id: 17455987, UMLKSK CUI: C0887935
HumanCTNNA11495catenin (cadherin-associated protein), alpha 1, 102kDa
img GENERIF, Score=1000, Pubmed Id: 15297182, UMLKSK CUI: C0887935
HumanKLF61316Kruppel-like factor 6
img GENERIF, Score=1000, Pubmed Id: 15057748, UMLKSK CUI: C0887935
img GENERIF, Score=901, Pubmed Id: 17514651, UMLKSK CUI: C0887935
HumanBRCA2675breast cancer 2, early onset
img GENERIF, Score=694, Pubmed Id: 18204050, UMLKSK CUI: C0887935
HumanAPC324adenomatous polyposis coli
img GENERIF, Score=1000, Pubmed Id: 16426911, UMLKSK CUI: C0887935
HumanAPAF1317apoptotic peptidase activating factor 1
img GENERIF, Score=1000, Pubmed Id: 15026369, UMLKSK CUI: C0887935
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0887935Allelic Imbalance0self