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Details
Link-It Detail - Disease - Dysequilibrium
Debug Stats
  • ### Total Build Time: 28 ms 27.646 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=0 Completed: 0 ms rowSize= 14 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=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 26.006 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Dysequilibrium C0281825
Genes (22)

Species:
human : 22
SpeciesGeneGeneIdGene NameEvidence
HumanDYX1C1161582dyslexia susceptibility 1 candidate 1
img GENERIF, Score=1000, Pubmed Id: 17309662, UMLKSK CUI: C0281825
img GENERIF, Score=861, Pubmed Id: 17450541, UMLKSK CUI: C0281825
HumanUGT1A954600UDP glucuronosyltransferase 1 family, polypeptide A9
img GENERIF, Score=827, Pubmed Id: 17761781, UMLKSK CUI: C0281825
HumanUSH1C10083Usher syndrome 1C (autosomal recessive, severe)
img GENERIF, Score=827, Pubmed Id: 11810303, UMLKSK CUI: C0281825
HumanCACNA1H8912calcium channel, voltage-dependent, T type, alpha 1H subunit
img GENERIF, Score=660, Pubmed Id: 17156077, UMLKSK CUI: C0281825
HumanTNXB7148tenascin XB
img GENERIF, Score=660, Pubmed Id: 14729256, UMLKSK CUI: C0281825
HumanSLC6A46532solute carrier family 6 (neurotransmitter transporter), member 4
img GENERIF, Score=660, Pubmed Id: 16082698, UMLKSK CUI: C0281825
img GENERIF, Score=660, Pubmed Id: 11920155, UMLKSK CUI: C0281825
HumanSLC6A36531solute carrier family 6 (neurotransmitter transporter), member 3
img GENERIF, Score=861, Pubmed Id: 18446263, UMLKSK CUI: C0281825
HumanSHOX6473short stature homeobox
img GENERIF, Score=694, Pubmed Id: 12089524, UMLKSK CUI: C0281825
HumanPTH1R5745parathyroid hormone 1 receptor
img GENERIF, Score=660, Pubmed Id: 15294324, UMLKSK CUI: C0281825
HumanPKLR5313pyruvate kinase, liver and RBC
img GENERIF, Score=812, Pubmed Id: 12107439, UMLKSK CUI: C0281825
HumanMYO9B4650myosin IXB
img GENERIF, Score=660, Pubmed Id: 16943798, UMLKSK CUI: C0281825
HumanMTHFR4524methylenetetrahydrofolate reductase (NAD(P)H)
img GENERIF, Score=694, Pubmed Id: 13678724, UMLKSK CUI: C0281825
HumanLPL4023lipoprotein lipase
img GENERIF, Score=660, Pubmed Id: 15127290, UMLKSK CUI: C0281825
HumanIL4R3566interleukin 4 receptor
img GENERIF, Score=660, Pubmed Id: 16538488, UMLKSK CUI: C0281825
HumanHLA-DRB13123
img GENERIF, Score=660, Pubmed Id: 18000641, UMLKSK CUI: C0281825
img GENERIF, Score=660, Pubmed Id: 12039413, UMLKSK CUI: C0281825
HumanGRIK22898glutamate receptor, ionotropic, kainate 2
img GENERIF, Score=827, Pubmed Id: 15305151, UMLKSK CUI: C0281825
HumanGJB22706gap junction protein, beta 2, 26kDa
img GENERIF, Score=1000, Pubmed Id: 12497637, UMLKSK CUI: C0281825
HumanCRY11407cryptochrome 1 (photolyase-like)
img GENERIF, Score=660, Pubmed Id: 15722957, UMLKSK CUI: C0281825
HumanCOMT1312catechol-O-methyltransferase
img GENERIF, Score=660, Pubmed Id: 16231731, UMLKSK CUI: C0281825
HumanCHAT1103choline O-acetyltransferase
img GENERIF, Score=827, Pubmed Id: 12759818, UMLKSK CUI: C0281825
HumanAVPR1A552arginine vasopressin receptor 1A
img GENERIF, Score=660, Pubmed Id: 12082568, UMLKSK CUI: C0281825
HumanARVCF421armadillo repeat gene deleted in velocardiofacial syndrome
img GENERIF, Score=827, Pubmed Id: 16118784, UMLKSK CUI: C0281825
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0281825Dysequilibrium0self