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Details
Link-It Detail - Jax Mouse Phenotype - abnormal erythrocyte morphology
Debug Stats
  • ### Total Build Time: 523 ms 32.378 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 430 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=0 Completed: 0 ms rowSize= 578 bytes
  • CONCEPT_CHILDREN gt=14 ms Completed: 14 ms rowSize= 12.298 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.575 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=503 ms Completed: 503 ms rowSize= 15.647 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal erythrocyte morphology MP:0002447
Definition (1)
any structural anomaly of a mature red blood cell, an ennucleate biconcave disk about 7 micrometers in diameter that contains hemoglobin confined within a lipid membrane; it is the major cellular element of the circulating blood and transports oxygen as its principal function
Synonyms (1)
"erythrocyte abnormalities" BROAD
Parents (1)
img abnormal erythropoiesis MP:0000245
Children (27)
img poikilocytosis MP:0002643
img acanthocytosis MP:0010177
img echinocytosis MP:0000256
img increased number of Howell-Jolly bodies MP:0010178
img microcytosis MP:0002813
img increased nucleated erythrocyte cell number MP:0009395
img abnormal red blood cell deformability MP:0009568
img leptocytosis MP:0010175
img abnormal mean corpuscular volume MP:0000226
img macrocytosis MP:0000248
img stomatocytosis MP:0010074
img abnormal hemoglobin MP:0001588
img anemia MP:0001577
img abnormal hemoglobin concentration distribution width MP:0008849
img abnormal fetal derived definitive erythrocyte morphology MP:0011240
img abnormal erythrocyte cell number MP:0001586
img polychromatophilia MP:0005097
img spherocytosis MP:0002812
img dacryocytosis MP:0010176
img increased number of Heinz bodies MP:0011171
img elliptocytosis MP:0009547
img abnormal hematocrit MP:0002596
img hyperchromasia MP:0002814
img increased siderocyte number MP:0010696
img anisopoikilocytosis MP:0002641
img abnormal red blood cell distribution width MP:0010066
img increased erythrocyte protoporphyrin level MP:0011188
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053977img abnormal erythropoiesis MP:0000245
Genes (425)

Species:
human : 425
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanGIMAP1-GIMAP5100527949
Click here to display 182 evidence detail records.
HumanPIM3415116pim-3 oncogene
INFERRED
HumanTSPAN33340348tetraspanin 33
Click here to display 182 evidence detail records.
HumanATP11C286410ATPase, class VI, type 11C
INFERRED
HumanBCL6B255877B-cell CLL/lymphoma 6, member B
INFERRED
HumanUNC13D201294unc-13 homolog D (C. elegans)
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanDHX36170506DEAH (Asp-Glu-Ala-His) box polypeptide 36
INFERRED
HumanTMPRSS6164656transmembrane protease, serine 6
Click here to display 182 evidence detail records.
HumanZFPM1161882zinc finger protein, FOG family member 1
INFERRED
HumanRC3H1149041ring finger and CCCH-type domains 1
INFERRED
HumanHFE2148738hemochromatosis type 2 (juvenile)
INFERRED
HumanCCBE1147372collagen and calcium binding EGF domains 1
INFERRED
HumanEDARADD128178EDAR-associated death domain
INFERRED
HumanMSI2124540musashi RNA-binding protein 2
INFERRED
HumanPTPMT1114971protein tyrosine phosphatase, mitochondrial 1
INFERRED
HumanEGLN2112398egl-9 family hypoxia-inducible factor 2
INFERRED
HumanPPP1R15B84919protein phosphatase 1, regulatory subunit 15B
Click here to display 182 evidence detail records.
HumanSLX484464SLX4 structure-specific endonuclease subunit
INFERRED
HumanL3MBTL384456l(3)mbt-like 3 (Drosophila)
INFERRED
HumanDOT1L84444DOT1-like histone H3K79 methyltransferase
INFERRED
HumanFERMT383706fermitin family member 3
Click here to display 182 evidence detail records.
HumanUNC93B181622unc-93 homolog B1 (C. elegans)
INFERRED
HumanZC3H12A80149zinc finger CCCH-type containing 12A
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002447abnormal erythrocyte morphology0self