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Details
Link-It Detail - Jax Mouse Phenotype - abnormal mean corpuscular volume
Debug Stats
  • ### Total Build Time: 69 ms 19.702 KB
  • CONCEPT_NAME gt=14 ms Completed: 14 ms rowSize= 392 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 314 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 183 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=7 ms Completed: 7 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.035 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=35 ms Completed: 35 ms rowSize= 14.329 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.170 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal mean corpuscular volume MP:0000226
Definition (1)
deviation from normal for the average amount of space occupied by each red blood cell, calculated from the hematocrit and red cell count, in erythrocyte indices
Synonyms (1)
"abnormal mean cell volume" EXACT
Parents (1)
img abnormal erythrocyte morphology MP:0002447
Children (2)
img increased mean corpuscular volume MP:0002590
img decreased mean corpuscular volume MP:0002591
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053978img abnormal erythrocyte morphology MP:0002447
Genes (75)

Species:
human : 75
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPIM3415116pim-3 oncogene
INFERRED
HumanDHX36170506DEAH (Asp-Glu-Ala-His) box polypeptide 36
INFERRED
HumanTMPRSS6164656transmembrane protease, serine 6
INFERRED
HumanHFE2148738hemochromatosis type 2 (juvenile)
INFERRED
HumanPPP1R15B84919protein phosphatase 1, regulatory subunit 15B
INFERRED
HumanRHBDF164285rhomboid 5 homolog 1 (Drosophila)
INFERRED
HumanSMAP160682small ArfGAP 1
INFERRED
HumanRANBP1057610RAN binding protein 10
INFERRED
HumanTTC7A57217tetratricopeptide repeat domain 7A
INFERRED
HumanGPRC5C55890G protein-coupled receptor, family C, group 5, member C
INFERRED
HumanSTEAP355240STEAP family member 3, metalloreductase
INFERRED
HumanEXOC654536exocyst complex component 6
INFERRED
HumanBCL11A53335B-cell CLL/lymphoma 11A (zinc finger protein)
INFERRED
HumanKLF1351621Kruppel-like factor 13
INFERRED
HumanSLC25A3751312solute carrier family 25 (mitochondrial iron transporter), member 37
INFERRED
HumanFOXP350943forkhead box P3
INFERRED
HumanSLC40A130061solute carrier family 40 (iron-regulated transporter), member 1
INFERRED
HumanDKK327122dickkopf WNT signaling pathway inhibitor 3
INFERRED
HumanEIF2AK127102eukaryotic translation initiation factor 2-alpha kinase 1
INFERRED
HumanPPP1R15A23645protein phosphatase 1, regulatory subunit 15A
INFERRED
HumanCLEC10A10462C-type lectin domain family 10, member A
INFERRED
HumanHEPH9843hephaestin
INFERRED
HumanULK18408unc-51 like autophagy activating kinase 1
INFERRED
HumanNPRL38131nitrogen permease regulator-like 3 (S. cerevisiae)
INFERRED
HumanTRPC37222transient receptor potential cation channel, subfamily C, member 3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000226abnormal mean corpuscular volume0self