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 chromosome segregation
Debug Stats
  • ### Total Build Time: 30 ms 28.930 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 212 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=4 ms Completed: 4 ms rowSize= 791 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.137 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.104 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 22.533 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.031 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of chromosome segregation HP:0002916
Parents (2)
img Abnormality of metabolism/homeostasis HP:0001939
img Abnormality of cell physiology HP:0011017
Children (6)
img Increased rate of premature chromosome condensation HP:0003451
img Endopolyploidy on chromosome studies of bone marrow HP:0003352
img Folate-dependent fragile site at Xq28 HP:0003564
img Abnormality of chromosome stability HP:0003220
img Premature chromatid separation HP:0200024
img Loss of heterozygosity, multiple chromosomes HP:0003494
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of metabolism/homeostasis HP:0001939
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of cell physiology HP:0011017
Genes (82)

Species:
human : 82
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUP16P11.2100909384
img HP TAS, OMIM ID: 614671
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP TAS, OMIM ID: 614526
HumanDUPXQ27.3Q28100874533
img HP TAS, OMIM ID: 300869
HumanDEL17Q11.2100852404
img HP TAS, OMIM ID: 613675
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP TAS, OMIM ID: 252270
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP TAS, OMIM ID: 613884
HumanDUP17Q21.31100529226
img HP TAS, OMIM ID: 613533
HumanDUP17Q23.1Q23.2100526743
img HP TAS, OMIM ID: 613618
HumanDUPXQ28100415893Chromosome Xq28 duplication syndrome
img HP TAS, OMIM ID: 300815
HumanDUPXP11.23P11.22100310754
img HP TAS, OMIM ID: 300801
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP TAS, OMIM ID: 158170
HumanDEL18P100240747Chromosome 18p deletion syndrome
img HP TAS, OMIM ID: 146390
HumanDUP22Q11.2100240738
img HP TAS, OMIM ID: 608363
HumanDUP1Q21100217371Chromosome 1q21.1 duplication syndrome
img HP TAS, OMIM ID: 612475
HumanDUP3Q29100188862chromosome 3q29 microduplication syndrome
img HP TAS, OMIM ID: 611936
HumanSHFM3100049542Split-hand/foot malformation 3
img HP TAS, OMIM ID: 246560
HumanPTLS100038247Potocki-Lupski syndrome
img HP TAS, OMIM ID: 610883
HumanSNORD116-1100033413
img HP TAS, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP TAS, OMIM ID: 176270
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
img HP RolledUp, OMIM ID: 601675
HumanSNORD115-1338433
img HP TAS, OMIM ID: 176270
HumanWDR62284403WD repeat domain 62
img HP RolledUp, OMIM ID: 251200
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
img HP RolledUp, OMIM ID: 269000
img HP RolledUp, OMIM ID: 268300
HumanCDAN1146059codanin 1
img HP RolledUp, OMIM ID: 224120
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP TAS, OMIM ID: 176270
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002916Abnormality of chromosome segregation0self