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Details
Link-It Detail - CoExpression - Genes changed in the B cell chronic lymphocytic leukemia (B-CLL) with deletions in the 17p13 region.
Debug Stats
  • ### Total Build Time: 33 ms 12.339 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 294 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=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=26 ms Completed: 26 ms rowSize= 10.728 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
CoExpression (1)
Genes changed in the B cell chronic lymphocytic leukemia (B-CLL) with deletions in the 17p13 region. haslinger_b_cll_with_17p13_deletion
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanGEMIN450628gem (nuclear organelle) associated protein 4
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanSENP326168SUMO1/sentrin/SMT3 specific peptidase 3
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanMAPRE322924microtubule-associated protein, RP/EB family, member 3
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanGABARAP11337GABA(A) receptor-associated protein
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanPRDX410549peroxiredoxin 4
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanHNRNPDL9987heterogeneous nuclear ribonucleoprotein D-like
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanFXR29513fragile X mental retardation, autosomal homolog 2
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanASMTL8623acetylserotonin O-methyltransferase-like
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanVDAC17416voltage-dependent anion channel 1
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanTP537157tumor protein p53
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanSCP26342sterol carrier protein 2
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanRYR16261ryanodine receptor 1 (skeletal)
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanPLD25338phospholipase D2
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanGPS22874G protein pathway suppressor 2
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanGNAI22771guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 2
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
HumanEIF4A11973eukaryotic translation initiation factor 4A1
MSigDB: C2.cgp, coexpatlas Id: haslinger_b_cll_with_17p13_deletion
XRefs (1)

XRef Types:
coexp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
COEXPimg haslinger_b_cll_with_17p13_deletionGenes changed in the B cell chronic lymphocytic leukemia (B-CLL) with deletions in the 17p13 region.0self