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Details
Link-It Detail - Human Phenotype - Abnormality of T cell number
Debug Stats
  • ### Total Build Time: 11 ms 20.853 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 203 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=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= 443 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.095 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.007 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 14.953 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.022 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of T cell number HP:0011839
Parents (1)
img Abnormality of T cells HP:0002843
Children (3)
img Increase in T cell number HP:0100828
img T lymphocytopenia HP:0005403
img Increased proportion of HLA DR+ and CD57+ T cells HP:0002853
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of T cells HP:0002843
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of T cells HP:0002843
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of T cells HP:0002843
Genes (22)

Species:
human : 22
SpeciesGeneGeneIdGene NameEvidence
HumanMAGT184061magnesium transporter 1
img HP RolledUp, OMIM ID: 300853
HumanEPG557724ectopic P-granules autophagy protein 5 homolog (C. elegans)
img HP RolledUp, OMIM ID: 242840
HumanWIPF17456WAS/WASL interacting protein family, member 1
img HP RolledUp, OMIM ID: 614493
HumanRAG25897recombination activating gene 2
img HP RolledUp, OMIM ID: 233650
HumanRAG15896recombination activating gene 1
img HP RolledUp, OMIM ID: 233650
HumanPTPRC5788protein tyrosine phosphatase, receptor type, C
HumanNBN4683nibrin
img HP RolledUp, OMIM ID: 251260
HumanIL7R3575interleukin 7 receptor
HumanIL2RG3561interleukin 2 receptor, gamma
img HP RolledUp, OMIM ID: 312863
HumanIL2RA3559interleukin 2 receptor, alpha
img HP RolledUp, OMIM ID: 606367
HumanDNMT3B1789DNA (cytosine-5-)-methyltransferase 3 beta
img HP RolledUp, OMIM ID: 242860
HumanCD40LG959CD40 ligand
HumanCD8A925CD8a molecule
img HP RolledUp, OMIM ID: 608957
HumanCD247919CD247 molecule
img HP RolledUp, OMIM ID: 610163
HumanCD3E916CD3e molecule, epsilon (CD3-TCR complex)
HumanCD3D915CD3d molecule, delta (CD3-TCR complex)
HumanCASP10843caspase 10, apoptosis-related cysteine peptidase
img HP RolledUp, OMIM ID: 603909
HumanCASP8841caspase 8, apoptosis-related cysteine peptidase
HumanATM472ataxia telangiectasia mutated
HumanFASLG356Fas ligand (TNF superfamily, member 6)
img HP RolledUp, OMIM ID: 601859
HumanFAS355Fas cell surface death receptor
img HP RolledUp, OMIM ID: 601859
HumanACP554acid phosphatase 5, tartrate resistant
img HP RolledUp, OMIM ID: 607944
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011839Abnormality of T cell number0self