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Details
Link-It Detail - Human Phenotype - Abnormality of reticulocytes
Debug Stats
  • ### Total Build Time: 28 ms 27.651 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 203 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 196 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=4 ms Completed: 4 ms rowSize= 448 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 758 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 2.092 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 22.825 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.022 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of reticulocytes HP:0004312
Definition (1)
A `reticulocyte` (CL:0000558) abnormality.
Parents (1)
img Abnormality of erythrocytes HP:0001877
Children (2)
img Reticulocytopenia HP:0001896
img Reticulocytosis HP:0001923
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of erythrocytes HP:0001877
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of erythrocytes HP:0001877
Genes (34)

Species:
human : 34
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDBA2114086Diamond-Blackfan anemia 2
img HP RolledUp, OMIM ID: 105650
HumanABCG864241ATP-binding cassette, sub-family G (WHITE), member 8
img HP RolledUp, OMIM ID: 210250
HumanABCG564240ATP-binding cassette, sub-family G (WHITE), member 5
img HP RolledUp, OMIM ID: 210250
HumanADAMTS1311093ADAM metallopeptidase with thrombospondin type 1 motif, 13
img HP RolledUp, OMIM ID: 274150
HumanCFHR310878complement factor H-related 3
img HP RolledUp, OMIM ID: 235400
HumanDHS10774dehydrated hereditary stomatocytosis
img HP RolledUp, OMIM ID: 194380
HumanKLF110661Kruppel-like factor 1 (erythroid)
img HP RolledUp, OMIM ID: 613673
HumanSEC23B10483Sec23 homolog B (S. cerevisiae)
img HP RolledUp, OMIM ID: 224100
HumanPIEZO19780piezo-type mechanosensitive ion channel component 1
img HP RolledUp, OMIM ID: 194380
HumanTCN26948transcobalamin II
img HP RolledUp, OMIM ID: 275350
HumanSLC4A16521solute carrier family 4 (anion exchanger), member 1
img HP RolledUp, OMIM ID: 109270
img HP RolledUp, OMIM ID: 612653
HumanSLC2A16513solute carrier family 2 (facilitated glucose transporter), member 1
img HP RolledUp, OMIM ID: 612126
HumanRPS246229ribosomal protein S24
img HP RolledUp, OMIM ID: 610629
HumanRPS196223ribosomal protein S19
img HP RolledUp, OMIM ID: 105650
HumanRPS176218ribosomal protein S17
img HP RolledUp, OMIM ID: 612527
HumanPKLR5313pyruvate kinase, liver and RBC
img HP RolledUp, OMIM ID: 266200
HumanPGK15230phosphoglycerate kinase 1
img HP RolledUp, OMIM ID: 300653
HumanPFKM5213phosphofructokinase, muscle
img HP RolledUp, OMIM ID: 232800
HumanCD464179CD46 molecule, complement regulatory protein
img HP RolledUp, OMIM ID: 235400
HumanCFI3426complement factor I
img HP RolledUp, OMIM ID: 235400
HumanCFHR13078complement factor H-related 1
img HP RolledUp, OMIM ID: 235400
HumanCFH3075complement factor H
img HP RolledUp, OMIM ID: 235400
HumanHBG23048hemoglobin, gamma G
img HP RolledUp, OMIM ID: 613977
HumanGATA12623GATA binding protein 1 (globin transcription factor 1)
img HP IEA, OMIM ID: 300835
img HP RolledUp, OMIM ID: 314050
HumanFANCG2189Fanconi anemia, complementation group G
img HP RolledUp, OMIM ID: 227650
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0004312Abnormality of reticulocytes0self