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 the cerebral vasculature
Debug Stats
  • ### Total Build Time: 23 ms 28.624 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 214 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=2 ms Completed: 2 ms rowSize= 1.115 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.071 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 3.984 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 21.066 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.033 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the cerebral vasculature HP:0100659
Parents (3)
img Abnormality of the cerebellum HP:0001317
img Abnormality of the vasculature HP:0002597
img Morphological abnormality of the central nervous system HP:0007319
Children (3)
img Stroke HP:0001297
img Intracranial hemorrhage HP:0002170
img Abnormalities of the cerebral arteries HP:0009145
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the cerebellum HP:0001317
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the cerebellum HP:0001317
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the vasculature HP:0002597
img All HP:0000001img Phenotypic abnormality HP:00001186img Morphological abnormality of the central nervous system HP:0007319
Genes (130)

Species:
human : 130
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanHHT4791087Telangiectasia, hereditary hemorrhagic, type 4
img HP RolledUp, OMIM ID: 610655
HumanWG474168Wegener granulomatosis
img HP RolledUp, OMIM ID: 608710
HumanCMAL246230Capillary malformations, hereditary
img HP RolledUp, OMIM ID: 163000
HumanANIB1116833aneurysm, intracranial berry 1
img HP RolledUp, OMIM ID: 105800
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanANTXR184168anthrax toxin receptor 1
img HP TAS, OMIM ID: 230740
HumanCCM283605cerebral cavernous malformation 2
img HP RolledUp, OMIM ID: 603284
HumanDOCK881704dedicator of cytokinesis 8
HumanSLC2A1081031solute carrier family 2 (facilitated glucose transporter), member 10
img HP RolledUp, OMIM ID: 208050
HumanXYLT264132xylosyltransferase II
img HP RolledUp, OMIM ID: 264800
HumanXYLT164131xylosyltransferase I
img HP RolledUp, OMIM ID: 264800
HumanTBC1D2457465TBC1 domain family, member 24
img HP RolledUp, OMIM ID: 605021
HumanTMEM12755654transmembrane protein 127
HumanEIM54119Infantile myoclonic epilepsy
img HP RolledUp, OMIM ID: 605021
HumanPRKAG251422protein kinase, AMP-activated, gamma 2 non-catalytic subunit
img HP RolledUp, OMIM ID: 194200
HumanMLXIPL51085MLX interacting protein-like
img HP RolledUp, OMIM ID: 194050
HumanSMARCAL150485SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
HumanCD20930835CD209 molecule
img HP RolledUp, OMIM ID: 614371
HumanACAD928976acyl-CoA dehydrogenase family, member 9
img HP RolledUp, OMIM ID: 611126
HumanKIF1B23095kinesin family member 1B
HumanTREX111277three prime repair exonuclease 1
img HP RolledUp, OMIM ID: 192315
HumanPDCD1011235programmed cell death 10
img HP RolledUp, OMIM ID: 603285
HumanSEC6311231SEC63 homolog (S. cerevisiae)
HumanSLC19A210560solute carrier family 19 (thiamine transporter), member 2
img HP RolledUp, OMIM ID: 249270
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100659Abnormality of the cerebral vasculature0self