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Details
Link-It Detail - Jax Mouse Phenotype - chromosome breakage
Debug Stats
  • ### Total Build Time: 208 ms 20.831 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 366 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 266 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=10 ms Completed: 10 ms rowSize= 578 bytes
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 1.027 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=21 ms Completed: 21 ms rowSize= 1.563 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=156 ms Completed: 156 ms rowSize= 15.757 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
chromosome breakage MP:0004028
Definition (1)
chromosome instability in the form of increased frequency of spontaneous breakage with or without rearrangements
Parents (1)
img chromosomal instability MP:0008866
Children (2)
img induced chromosome breakage MP:0004030
img spontaneous chromosome breakage MP:0004029
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053846img chromosomal instability MP:0008866
Genes (58)

Species:
human : 58
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMCM9254394minichromosome maintenance complex component 9
INFERRED
HumanMCM884515minichromosome maintenance complex component 8
INFERRED
HumanMUS8180198MUS81 structure-specific endonuclease subunit
Click here to display 50 evidence detail records.
HumanNHEJ179840nonhomologous end-joining factor 1
INFERRED
HumanMCPH179648microcephalin 1
INFERRED
HumanDCLRE1C64421DNA cross-link repair 1C
INFERRED
HumanAICDA57379activation-induced cytidine deaminase
INFERRED
HumanCHFR55743checkpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase
Click here to display 50 evidence detail records.
HumanUIMC151720ubiquitin interaction motif containing 1
Click here to display 50 evidence detail records.
HumanSIRT651548sirtuin 6
INFERRED
HumanLATS226524large tumor suppressor kinase 2
Click here to display 50 evidence detail records.
HumanPOT125913protection of telomeres 1
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HumanCOPS510987COP9 signalosome subunit 5
INFERRED
HumanPOLQ10721polymerase (DNA directed), theta
Click here to display 50 evidence detail records.
HumanRAD5010111RAD50 homolog (S. cerevisiae)
Click here to display 50 evidence detail records.
HumanPARP210038poly (ADP-ribose) polymerase 2
INFERRED
HumanMDC19656mediator of DNA-damage checkpoint 1
INFERRED
HumanRECQL49401RecQ protein-like 4
Click here to display 50 evidence detail records.
HumanSMC1A8243structural maintenance of chromosomes 1A
Click here to display 50 evidence detail records.
HumanXRCC57520X-ray repair complementing defective repair in Chinese hamster cells 5 (double-strand-break rejoining)
Click here to display 50 evidence detail records.
HumanXRCC47518X-ray repair complementing defective repair in Chinese hamster cells 4
INFERRED
HumanUSP17398ubiquitin specific peptidase 1
INFERRED
HumanTYR7299tyrosinase
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HumanTP53BP17158tumor protein p53 binding protein 1
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HumanTP537157tumor protein p53
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004028chromosome breakage0self