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Details
Link-It Detail - Jax Mouse Phenotype - abnormal thrombopoiesis
Debug Stats
  • ### Total Build Time: 119 ms 21.485 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 374 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 270 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 192 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=12 ms Completed: 12 ms rowSize= 1.022 KB
  • CONCEPT_CHILDREN gt=9 ms Completed: 9 ms rowSize= 585 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=16 ms Completed: 16 ms rowSize= 2.925 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=72 ms Completed: 72 ms rowSize= 14.845 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.161 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal thrombopoiesis MP:0000228
Definition (1)
abnormal development of the non-nucleated cells of the blood (platelets, thrombocytes) involved in blood coagulation
Synonyms (1)
"abnormal thrombocyte development" RELATED
Parents (2)
img abnormal hematopoiesis MP:0002123
img abnormal megakaryocyte morphology MP:0002417
Children (1)
img abnormal platelet morphology MP:0004720
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053976img abnormal hematopoiesis MP:0002123
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053977img abnormal megakaryocyte morphology MP:0002417
Genes (181)

Species:
human : 181
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGIMAP1-GIMAP5100527949
INFERRED
HumanTSPAN33340348tetraspanin 33
INFERRED
HumanTREML1340205triggering receptor expressed on myeloid cells-like 1
INFERRED
HumanSLC35D3340146solute carrier family 35, member D3
INFERRED
HumanUNC13D201294unc-13 homolog D (C. elegans)
INFERRED
HumanZFPM1161882zinc finger protein, FOG family member 1
INFERRED
HumanRC3H1149041ring finger and CCCH-type domains 1
INFERRED
HumanTOM1L2146691target of myb1-like 2 (chicken)
INFERRED
HumanSIRPA140885signal-regulatory protein alpha
INFERRED
HumanNLRP3114548NLR family, pyrin domain containing 3
INFERRED
HumanHPS489781Hermansky-Pudlak syndrome 4
INFERRED
HumanDOCK785440dedicator of cytokinesis 7
INFERRED
HumanORAI184876ORAI calcium release-activated calcium modulator 1
INFERRED
HumanSPSB284727splA/ryanodine receptor domain and SOCS box containing 2
INFERRED
HumanKISS1R84634KISS1 receptor
INFERRED
HumanSLX484464SLX4 structure-specific endonuclease subunit
INFERRED
HumanHPS384343Hermansky-Pudlak syndrome 3
INFERRED
HumanDTNBP184062dystrobrevin binding protein 1
INFERRED
HumanUNC93B181622unc-93 homolog B1 (C. elegans)
INFERRED
HumanTUBB181027tubulin, beta 1 class VI
INFERRED
HumanZC3H12A80149zinc finger CCCH-type containing 12A
INFERRED
HumanHPS679803Hermansky-Pudlak syndrome 6
INFERRED
HumanKXD179036KxDL motif containing 1
INFERRED
HumanSOX1764321SRY (sex determining region Y)-box 17
INFERRED
HumanABCG864241ATP-binding cassette, sub-family G (WHITE), member 8
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000228abnormal thrombopoiesis0self