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Details
Link-It Detail - Jax Mouse Phenotype - abnormal red blood cell distribution width
Debug Stats
  • ### Total Build Time: 22 ms 19.813 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 412 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 258 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 198 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=3 ms Completed: 3 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 1.055 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 14.432 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.180 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal red blood cell distribution width MP:0010066
Definition (1)
an anomaly in the coefficient of variance (reference range) of the red blood cell volume for an organism
Synonyms (1)
"abnormal red blood cell size variability" EXACT
Parents (1)
img abnormal erythrocyte morphology MP:0002447
Children (2)
img decreased red blood cell distribution width MP:0010068
img increased red blood cell distribution width MP:0010067
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053978img abnormal erythrocyte morphology MP:0002447
Genes (51)

Species:
human : 51
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGIMAP1-GIMAP5100527949
INFERRED
HumanTMPRSS6164656transmembrane protease, serine 6
INFERRED
HumanZFPM1161882zinc finger protein, FOG family member 1
INFERRED
HumanHFE2148738hemochromatosis type 2 (juvenile)
INFERRED
HumanABCG564240ATP-binding cassette, sub-family G (WHITE), member 5
INFERRED
HumanTTC7A57217tetratricopeptide repeat domain 7A
INFERRED
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED
HumanCDK5RAP255755CDK5 regulatory subunit associated protein 2
INFERRED
HumanEXOC654536exocyst complex component 6
INFERRED
HumanKLF1351621Kruppel-like factor 13
INFERRED
HumanFOXP350943forkhead box P3
INFERRED
HumanSLC40A130061solute carrier family 40 (iron-regulated transporter), member 1
INFERRED
HumanRASA322821RAS p21 protein activator 3
INFERRED
HumanKLF110661Kruppel-like factor 1 (erythroid)
INFERRED
HumanRB1CC19821RB1-inducible coiled-coil 1
INFERRED
HumanULK18408unc-51 like autophagy activating kinase 1
INFERRED
HumanNPRL38131nitrogen permease regulator-like 3 (S. cerevisiae)
INFERRED
HumanUROS7390uroporphyrinogen III synthase
INFERRED
HumanTF7018transferrin
INFERRED
HumanTAL16886T-cell acute lymphocytic leukemia 1
INFERRED
HumanSTAT5B6777signal transducer and activator of transcription 5B
INFERRED
HumanSTAT5A6776signal transducer and activator of transcription 5A
INFERRED
HumanSPTA16708spectrin, alpha, erythrocytic 1 (elliptocytosis 2)
INFERRED
HumanPROC5624protein C (inactivator of coagulation factors Va and VIIIa)
INFERRED
HumanPRKG15592protein kinase, cGMP-dependent, type I
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010066abnormal red blood cell distribution width0self