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Details
Link-It Detail - CoExpression - Down-regulated in B lymphocytes from patients with ICF syndrom caused by mutations in DNMT3B [Gene ID=1789] compared to normals.
Debug Stats
  • ### Total Build Time: 7 ms 9.448 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 309 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
  • CONCEPT_TEXT gt=NONE 1 ms 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=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 7.820 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
CoExpression (1)
Down-regulated in B lymphocytes from patients with ICF syndrom caused by mutations in DNMT3B [Gene ID=1789] compared to normals. ehrlich_icf_syndrom_dn
Genes (13)

Species:
human : 13
SpeciesGeneGeneIdGene NameEvidence
HumanBTN3A211118butyrophilin, subfamily 3, member A2
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanBTG27832BTG family, member 2
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanZFX7543zinc finger protein, X-linked
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanTFRC7037transferrin receptor (p90, CD71)
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanSLC1A16505solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanMEF2C4208myocyte enhancer factor 2C
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanITGB73695integrin, beta 7
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanINPP4A3631inositol polyphosphate-4-phosphatase, type I, 107kDa
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanIGHG33502immunoglobulin heavy constant gamma 3 (G3m marker)
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanID33399inhibitor of DNA binding 3, dominant negative helix-loop-helix protein
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanHMOX13162heme oxygenase (decycling) 1
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanCD27939CD27 molecule
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
HumanBLK640B lymphoid tyrosine kinase
MSigDB: C2.cgp, coexpatlas Id: ehrlich_icf_syndrom_dn
XRefs (1)

XRef Types:
coexp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
COEXPimg ehrlich_icf_syndrom_dnDown-regulated in B lymphocytes from patients with ICF syndrom caused by mutations in DNMT3B [Gene ID=1789] compared to normals.0self