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Details
Link-It Detail - Disease - Cognitive deficits
Debug Stats
  • ### Total Build Time: 8 ms 18.440 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 334 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=1 ms Completed: 1 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=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 16.788 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Cognitive deficits C0679466
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
img OMIM, Score=882, UMLKSK CUI: C0679466
HumanCTDP19150CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
img OMIM, Score=1000, UMLKSK CUI: C0679466
HumanEIF2B58893eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
img OMIM, Score=1000, UMLKSK CUI: C0679466
HumanEIF2B28892eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
img OMIM, Score=1000, UMLKSK CUI: C0679466
HumanEIF2B38891eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa
img OMIM, Score=1000, UMLKSK CUI: C0679466
HumanEIF2B48890eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
img OMIM, Score=1000, UMLKSK CUI: C0679466
HumanSLC6A36531solute carrier family 6 (neurotransmitter transporter), member 3
img GENERIF, Score=861, Pubmed Id: 15708296, UMLKSK CUI: C0679466
HumanGRM32913glutamate receptor, metabotropic 3
img GENERIF, Score=1000, Pubmed Id: 18197082, UMLKSK CUI: C0679466
HumanGLI32737GLI family zinc finger 3
img GENERIF, Score=1000, Pubmed Id: 14608643, UMLKSK CUI: C0679466
HumanEIF2B11967eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa
img OMIM, Score=1000, UMLKSK CUI: C0679466
HumanDYRK1A1859dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
img GENERIF, Score=1000, Pubmed Id: 15068245, UMLKSK CUI: C0679466
HumanDMPK1760dystrophia myotonica-protein kinase
img GENERIF, Score=861, Pubmed Id: 17433680, UMLKSK CUI: C0679466
HumanCOMT1312catechol-O-methyltransferase
img GENERIF, Score=1000, Pubmed Id: 17383818, UMLKSK CUI: C0679466
img GENERIF, Score=1000, Pubmed Id: 16476412, UMLKSK CUI: C0679466
HumanAPP351amyloid beta (A4) precursor protein
img GENERIF, Score=1000, Pubmed Id: 15282285, UMLKSK CUI: C0679466
img GENERIF, Score=1000, Pubmed Id: 16467370, UMLKSK CUI: C0679466
HumanAPOE348apolipoprotein E
img GENERIF, Score=901, Pubmed Id: 17250852, UMLKSK CUI: C0679466
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0679466Cognitive deficits0self