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Details
Link-It Detail - Jax Mouse Phenotype - abnormal chromosome morphology
Debug Stats
  • ### Total Build Time: 111 ms 21.096 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 274 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= 587 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 585 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.572 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=96 ms Completed: 96 ms rowSize= 16.420 KB
  • CONCEPT_XREFS gt=2 ms Completed: 1 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal chromosome morphology MP:0003702
Definition (1)
any structural anomaly of the compact, intertwined molecules of DNA found in the nucleus which carry genetic information
Parents (1)
img abnormal cell nucleus morphology MP:0003111
Children (1)
img abnormal telomere morphology MP:0010207
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053845img abnormal cell nucleus morphology MP:0003111
Genes (55)

Species:
human : 55
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanRAD21L1642636RAD21-like 1 (S. pombe)
INFERRED
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
Click here to display 60 evidence detail records.
HumanDOT1L84444DOT1-like histone H3K79 methyltransferase
INFERRED
HumanKAT884148K(lysine) acetyltransferase 8
Click here to display 60 evidence detail records.
HumanCTC180169CTS telomere maintenance complex component 1
INFERRED
HumanPIF180119PIF1 5'-to-3' DNA helicase
INFERRED
HumanMCPH179648microcephalin 1
Click here to display 60 evidence detail records.
HumanACD65057adrenocortical dysplasia homolog (mouse)
Click here to display 60 evidence detail records.
HumanSUDS364426suppressor of defective silencing 3 homolog (S. cerevisiae)
Click here to display 60 evidence detail records.
HumanPINX154984PIN2/TERF1 interacting, telomerase inhibitor 1
INFERRED
HumanTERF2IP54386telomeric repeat binding factor 2, interacting protein
INFERRED
HumanTDP251567tyrosyl-DNA phosphodiesterase 2
Click here to display 60 evidence detail records.
HumanPOT125913protection of telomeres 1
Click here to display 60 evidence detail records.
HumanSIRT123411sirtuin 1
Click here to display 60 evidence detail records.
HumanSIRT222933sirtuin 2
Click here to display 60 evidence detail records.
HumanDIDO111083death inducer-obliterator 1
Click here to display 60 evidence detail records.
HumanSTAG110274stromal antigen 1
INFERRED
HumanDCLRE1A9937DNA cross-link repair 1A
Click here to display 60 evidence detail records.
HumanESPL19700extra spindle pole bodies homolog 1 (S. cerevisiae)
Click here to display 60 evidence detail records.
HumanPTTG19232pituitary tumor-transforming 1
Click here to display 60 evidence detail records.
HumanBUB39184BUB3 mitotic checkpoint protein
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HumanRAD54L8438RAD54-like (S. cerevisiae)
Click here to display 60 evidence detail records.
HumanKAT6A7994K(lysine) acetyltransferase 6A
Click here to display 60 evidence detail records.
HumanTYR7299tyrosinase
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HumanTGFBI7045transforming growth factor, beta-induced, 68kDa
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XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003702abnormal chromosome morphology0self