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Details
Link-It Detail - Jax Mouse Phenotype - abnormal hemoglobin
Debug Stats
  • ### Total Build Time: 243 ms 20.667 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 366 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 238 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 177 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=4 ms Completed: 4 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.509 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=233 ms Completed: 233 ms rowSize= 14.938 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal hemoglobin MP:0001588
Definition (1)
defects in the levels or the function of the oxygen-carrying protein of erythrocytes
Synonyms (1)
"haemoglobin defects" EXACT
Parents (1)
img abnormal erythrocyte morphology MP:0002447
Children (3)
img abnormal mean corpuscular hemoglobin MP:0001589
img abnormal hemoglobin content MP:0005563
img abnormal mean corpuscular hemoglobin concentration MP:0005640
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053978img abnormal erythrocyte morphology MP:0002447
Genes (153)

Species:
human : 153
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGIMAP1-GIMAP5100527949
INFERRED
HumanDHX36170506DEAH (Asp-Glu-Ala-His) box polypeptide 36
INFERRED
HumanTMPRSS6164656transmembrane protease, serine 6
INFERRED
HumanZFPM1161882zinc finger protein, FOG family member 1
INFERRED
HumanHFE2148738hemochromatosis type 2 (juvenile)
INFERRED
HumanEGLN2112398egl-9 family hypoxia-inducible factor 2
INFERRED
HumanPPP1R15B84919protein phosphatase 1, regulatory subunit 15B
INFERRED
HumanZC3H12A80149zinc finger CCCH-type containing 12A
INFERRED
HumanRHBDF164285rhomboid 5 homolog 1 (Drosophila)
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
HumanGPRC5C55890G protein-coupled receptor, family C, group 5, member C
INFERRED
HumanSTEAP355240STEAP family member 3, metalloreductase
INFERRED
HumanTET254790tet methylcytosine dioxygenase 2
INFERRED
HumanEXOC654536exocyst complex component 6
INFERRED
HumanFGFRL153834fibroblast growth factor receptor-like 1
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
HumanCLEC1B51266C-type lectin domain family 1, member B
INFERRED
HumanFOXP350943forkhead box P3
INFERRED
HumanRRM2B50484ribonucleotide reductase M2 B (TP53 inducible)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001588abnormal hemoglobin0self