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Details
Link-It Detail - Human Phenotype - Abnormality of eosinophils
Debug Stats
  • ### Total Build Time: 23 ms 22.632 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 201 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 195 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=3 ms Completed: 3 ms rowSize= 448 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 435 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.021 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 17.196 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of eosinophils HP:0001879
Definition (1)
An `eosinophil` (CL:0000771) abnormality.
Parents (1)
img Abnormality of granulocytes HP:0001911
Children (1)
img Eosinophilia HP:0001880
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of granulocytes HP:0001911
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of granulocytes HP:0001911
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of granulocytes HP:0001911
Genes (21)

Species:
human : 21
SpeciesGeneGeneIdGene NameEvidence
HumanSLC46A1113235solute carrier family 46 (folate transporter), member 1
img HP TAS, OMIM ID: 229050
HumanDOCK881704dedicator of cytokinesis 8
img HP RolledUp, OMIM ID: 243700
HumanDCLRE1C64421DNA cross-link repair 1C
img HP TAS, OMIM ID: 603554
HumanRFMN57788Roifman syndrome
img HP RolledUp, OMIM ID: 300258
HumanRBM8A9939RNA binding motif protein 8A
img HP RolledUp, OMIM ID: 274000
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
img HP TAS, OMIM ID: 308300
HumanEOS7908eosinophilia, familial
img HP RolledUp, OMIM ID: 131400
HumanADAM176868ADAM metallopeptidase domain 17
img HP RolledUp, OMIM ID: 614328
HumanSTAT36774signal transducer and activator of transcription 3 (acute-phase response factor)
img HP TAS, OMIM ID: 147060
HumanRAG25897recombination activating gene 2
img HP TAS, OMIM ID: 603554
HumanRAG15896recombination activating gene 1
img HP TAS, OMIM ID: 603554
HumanPDGFRA5156platelet-derived growth factor receptor, alpha polypeptide
img HP RolledUp, OMIM ID: 607685
HumanMYH94627myosin, heavy chain 9, non-muscle
img HP TAS, OMIM ID: 153640
HumanGFI12672growth factor independent 1 transcription repressor
img HP RolledUp, OMIM ID: 202700
HumanELANE1991elastase, neutrophil expressed
img HP RolledUp, OMIM ID: 202700
img HP TAS, OMIM ID: 162800
HumanCD247919CD247 molecule
img HP RolledUp, OMIM ID: 610163
HumanCASP10843caspase 10, apoptosis-related cysteine peptidase
img HP RolledUp, OMIM ID: 603909
HumanCAPN3825calpain 3, (p94)
img HP RolledUp, OMIM ID: 253600
HumanFASLG356Fas ligand (TNF superfamily, member 6)
img HP RolledUp, OMIM ID: 601859
HumanFAS355Fas cell surface death receptor
img HP RolledUp, OMIM ID: 601859
HumanADA100adenosine deaminase
img HP RolledUp, OMIM ID: 102700
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001879Abnormality of eosinophils0self