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Details
Link-It Detail - Jax Mouse Phenotype - abnormal hematocrit
Debug Stats
  • ### Total Build Time: 31 ms 20.023 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 366 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 255 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= 586 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 1.010 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 14.950 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal hematocrit MP:0002596
Definition (1)
greater or less than the average percentage of a volume of a blood sample occupied by red blood cells
Parents (1)
img abnormal erythrocyte morphology MP:0002447
Children (2)
img increased hematocrit MP:0002608
img decreased hematocrit MP:0000208
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053978img abnormal erythrocyte morphology MP:0002447
Genes (163)

Species:
human : 163
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGIMAP1-GIMAP5100527949
INFERRED
HumanTSPAN33340348tetraspanin 33
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanTMPRSS6164656transmembrane protease, serine 6
INFERRED
HumanHFE2148738hemochromatosis type 2 (juvenile)
INFERRED
HumanCCBE1147372collagen and calcium binding EGF domains 1
INFERRED
HumanEGLN2112398egl-9 family hypoxia-inducible factor 2
INFERRED
HumanPPP1R15B84919protein phosphatase 1, regulatory subunit 15B
INFERRED
HumanZC3H12A80149zinc finger CCCH-type containing 12A
INFERRED
HumanABCG564240ATP-binding cassette, sub-family G (WHITE), member 5
INFERRED
HumanSMAP160682small ArfGAP 1
INFERRED
HumanTTC7A57217tetratricopeptide repeat domain 7A
INFERRED
HumanCIAPIN157019cytokine induced apoptosis inhibitor 1
INFERRED
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED
HumanKMT2E55904lysine (K)-specific methyltransferase 2E
INFERRED
HumanSTEAP355240STEAP family member 3, metalloreductase
INFERRED
HumanEGLN154583egl-9 family hypoxia-inducible factor 1
INFERRED
HumanFGFRL153834fibroblast growth factor receptor-like 1
INFERRED
HumanBCL11A53335B-cell CLL/lymphoma 11A (zinc finger protein)
INFERRED
HumanSLC25A3751312solute carrier family 25 (mitochondrial iron transporter), member 37
INFERRED
HumanCLEC1B51266C-type lectin domain family 1, member B
INFERRED
HumanFOXP350943forkhead box P3
INFERRED
HumanRRM2B50484ribonucleotide reductase M2 B (TP53 inducible)
INFERRED
HumanSLC40A130061solute carrier family 40 (iron-regulated transporter), member 1
INFERRED
HumanDKK327122dickkopf WNT signaling pathway inhibitor 3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002596abnormal hematocrit0self