Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Human Phenotype - Abnormality of granulocytes
Debug Stats
  • ### Total Build Time: 296 ms 30.267 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 202 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 200 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=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= 782 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.714 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 3.958 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 22.272 KB
  • CONCEPT_XREFS gt=266 ms Completed: 266 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of granulocytes HP:0001911
Definition (1)
An abnormality of `granulocytes` (CL:0000094).
Parents (2)
img Abnormality of myeloid leukocytes HP:0010974
img Abnormality of leukocytes HP:0001881
Children (5)
img Granulocytopenia HP:0001913
img Abnormality of basophils HP:0001912
img Abnormality of neutrophils HP:0001874
img Congenital agranulocytosis HP:0005541
img Abnormality of eosinophils HP:0001879
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of myeloid leukocytes HP:0010974
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of myeloid leukocytes HP:0010974
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of leukocytes HP:0001881
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of leukocytes HP:0001881
Genes (98)

Species:
human : 98
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNCF1653361neutrophil cytosolic factor 1
img HP RolledUp, OMIM ID: 233700
HumanMMAB326625methylmalonic aciduria (cobalamin deficiency) cblB type
img HP RolledUp, OMIM ID: 251110
HumanSUMF1285362sulfatase modifying factor 1
HumanUNC13D201294unc-13 homolog D (C. elegans)
img HP RolledUp, OMIM ID: 608898
HumanMMAA166785methylmalonic aciduria (cobalamin deficiency) cblA type
img HP RolledUp, OMIM ID: 251100
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
HumanNLRP3114548NLR family, pyrin domain containing 3
img HP RolledUp, OMIM ID: 607115
HumanDBA2114086Diamond-Blackfan anemia 2
img HP RolledUp, OMIM ID: 105650
HumanSLC46A1113235solute carrier family 46 (folate transporter), member 1
img HP RolledUp, OMIM ID: 229050
HumanG6PC392579glucose 6 phosphatase, catalytic, 3
img HP RolledUp, OMIM ID: 612541
HumanDOCK881704dedicator of cytokinesis 8
img HP RolledUp, OMIM ID: 243700
HumanUSB179650U6 snRNA biogenesis 1
img HP RolledUp, OMIM ID: 604173
HumanDCLRE1C64421DNA cross-link repair 1C
img HP RolledUp, OMIM ID: 603554
HumanRFMN57788Roifman syndrome
img HP RolledUp, OMIM ID: 300258
HumanLRRC8A56262leucine rich repeat containing 8 family, member A
img HP RolledUp, OMIM ID: 601495
HumanLMBRD155788LMBR1 domain containing 1
img HP RolledUp, OMIM ID: 277380
HumanSLC35C155343solute carrier family 35 (GDP-fucose transporter), member C1
img HP RolledUp, OMIM ID: 266265
HumanIRAK451135interleukin-1 receptor-associated kinase 4
img HP RolledUp, OMIM ID: 607676
HumanSBDS51119Shwachman-Bodian-Diamond syndrome
img HP RolledUp, OMIM ID: 260400
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
img HP RolledUp, OMIM ID: 242900
HumanICOS29851inducible T-cell co-stimulator
img HP RolledUp, OMIM ID: 607594
HumanBLNK29760B-cell linker
img HP RolledUp, OMIM ID: 613502
HumanLAMTOR228956late endosomal/lysosomal adaptor, MAPK and MTOR activator 2
img HP RolledUp, OMIM ID: 610798
HumanTINF226277TERF1 (TRF1)-interacting nuclear factor 2
img HP RolledUp, OMIM ID: 268130
HumanMMACHC25974methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
img HP RolledUp, OMIM ID: 277400
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001911Abnormality of granulocytes0self