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Details
Link-It Detail - Human Phenotype - Abnormality of the astrocytes
Debug Stats
  • ### Total Build Time: 21 ms 24.003 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 204 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 198 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 451 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 434 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.098 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 19.480 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.023 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the astrocytes HP:0100707
Definition (1)
An abnormality of `astrocytes` (CL:0000127).
Parents (1)
img Abnormality of the glial cells HP:0100705
Children (1)
img Astrocytoma HP:0009592
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the glial cells HP:0100705
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the glial cells HP:0100705
Genes (22)

Species:
human : 22
SpeciesGeneGeneIdGene NameEvidence
HumanRTE1404685repressor of telomerase expression 1
img HP RolledUp, OMIM ID: 137800
HumanGLM1338030Glioma, familial, 1
img HP RolledUp, OMIM ID: 137800
HumanWDR1155717WD repeat domain 11
img HP RolledUp, OMIM ID: 137800
HumanLGI19211leucine-rich, glioma inactivated 1
img HP RolledUp, OMIM ID: 137800
HumanTSC27249tuberous sclerosis 2
img HP RolledUp, OMIM ID: 613254
img HP RolledUp, OMIM ID: 191100
HumanTSC17248tuberous sclerosis 1
img HP RolledUp, OMIM ID: 191100
HumanTP537157tumor protein p53
img HP RolledUp, OMIM ID: 137800
HumanPTEN5728phosphatase and tensin homolog
img HP RolledUp, OMIM ID: 137800
HumanPPARG5468peroxisome proliferator-activated receptor gamma
img HP RolledUp, OMIM ID: 137800
HumanPMS25395PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
img HP RolledUp, OMIM ID: 276300
HumanNF24771neurofibromin 2 (merlin)
img HP RolledUp, OMIM ID: 101000
HumanNF14763neurofibromin 1
img HP RolledUp, OMIM ID: 162200
HumanMSH24436mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)
img HP RolledUp, OMIM ID: 162200
img HP RolledUp, OMIM ID: 276300
img HP RolledUp, OMIM ID: 137800
HumanMLH14292mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli)
img HP RolledUp, OMIM ID: 276300
HumanIFNG3458interferon, gamma
img HP RolledUp, OMIM ID: 191100
img HP RolledUp, OMIM ID: 613254
HumanIDH13417isocitrate dehydrogenase 1 (NADP+), soluble
img HP RolledUp, OMIM ID: 137800
HumanMSH62956mutS homolog 6 (E. coli)
img HP RolledUp, OMIM ID: 276300
HumanERBB22064v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 2
img HP RolledUp, OMIM ID: 137800
HumanDMBT11755deleted in malignant brain tumors 1
img HP RolledUp, OMIM ID: 137800
HumanCDKN2A1029cyclin-dependent kinase inhibitor 2A
img HP RolledUp, OMIM ID: 155755
HumanBRCA2675breast cancer 2, early onset
img HP RolledUp, OMIM ID: 137800
HumanAPC324adenomatous polyposis coli
img HP RolledUp, OMIM ID: 175100
img HP RolledUp, OMIM ID: 276300
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100707Abnormality of the astrocytes0self