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Details
Link-It Detail - CoExpression Atlas - Candidate genes in the pericentromeric microdeletion in 16p11.2-p12.2 associated with developmental disabilities.
Debug Stats
  • ### Total Build Time: 60 ms 12.977 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 332 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=9 ms Completed: 9 ms rowSize= 595 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=15 ms Completed: 15 ms rowSize= 1.368 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=31 ms Completed: 31 ms rowSize= 9.348 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.203 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
CoExpression Atlas (1)
Candidate genes in the pericentromeric microdeletion in 16p11.2-p12.2 associated with developmental disabilities. ballif_developmental_disability_p16_p12_deletion
Parents (1)
img coexpressionatlas_ballif_developmental_disability_p16_p12 ballif_developmental_disability_p16_p12
Ancestral Roots
RootRoot Plus OneDepthParent
img coexpressionatlas_ballif ballifimg coexpressionatlas_ballif_developmental ballif_developmental6img coexpressionatlas_ballif_developmental_disability_p16_p12 ballif_developmental_disability_p16_p12
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanOTOA146183otoancorin
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
HumanSLC5A11115584solute carrier family 5 (sodium/inositol cotransporter), member 11
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
HumanCOG791949component of oligomeric golgi complex 7
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
HumanKDM879831lysine (K)-specific demethylase 8
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
HumanIL21R50615interleukin 21 receptor
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
HumanTBX66911T-box 6
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
HumanSCNN1G6340sodium channel, non-voltage-gated 1, gamma subunit
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
HumanSCNN1B6338sodium channel, non-voltage-gated 1, beta subunit
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
HumanIL4R3566interleukin 4 receptor
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
HumanCLN31201ceroid-lipofuscinosis, neuronal 3
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
HumanATP2A1487ATPase, Ca++ transporting, cardiac muscle, fast twitch 1
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
HumanALDOA226aldolase A, fructose-bisphosphate
MSigDB: C2.cgp, coexpatlas Id: ballif_developmental_disability_p16_p12_deletion
XRefs (1)

XRef Types:
coexpatlas : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
coexpatlasimg ballif_developmental_disability_p16_p12_deletionCandidate genes in the pericentromeric microdeletion in 16p11.2-p12.2 associated with developmental disabilities.0self