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Details
Link-It Detail - Jax Mouse Phenotype - abnormal telomere morphology
Debug Stats
  • ### Total Build Time: 42 ms 24.049 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 384 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 356 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=0 Completed: 0 ms rowSize= 585 bytes
  • CONCEPT_CHILDREN gt=10 ms Completed: 10 ms rowSize= 581 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.570 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 19.307 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal telomere morphology MP:0010207
Definition (1)
any structural anomaly of the terminal repetitive DNA section of a chromosome which is involved in chromosomal replication and senescence, and which protects the end of the chromosome from deterioration
Parents (1)
img abnormal chromosome morphology MP:0003702
Children (1)
img abnormal telomere length MP:0003155
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053846img abnormal chromosome morphology MP:0003702
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanRAD21L1642636RAD21-like 1 (S. pombe)
img Jax MP, Pubmed Id: 20622869, MOUSE PHENOTYPE ID: MGI:1929871
img Jax MP, Pubmed Id: 21743440, MOUSE PHENOTYPE ID: MGI:3652039
img Jax MP, Pubmed Id: 22415365, MOUSE PHENOTYPE ID: MGI:1098658
img Jax MP, Pubmed Id: 20622869, MOUSE PHENOTYPE ID: MGI:1926776
img Jax MP, Pubmed Id: 22415365, MOUSE PHENOTYPE ID: MGI:1098658
HumanDOT1L84444DOT1-like histone H3K79 methyltransferase
INFERRED
HumanCTC180169CTS telomere maintenance complex component 1
INFERRED
HumanPIF180119PIF1 5'-to-3' DNA helicase
INFERRED
HumanPINX154984PIN2/TERF1 interacting, telomerase inhibitor 1
INFERRED
HumanTERF2IP54386telomeric repeat binding factor 2, interacting protein
img Jax MP, Pubmed Id: 22415365, MOUSE PHENOTYPE ID: MGI:1098658
img Jax MP, Pubmed Id: 20622869, MOUSE PHENOTYPE ID: MGI:1926776
img Jax MP, Pubmed Id: 22415365, MOUSE PHENOTYPE ID: MGI:1098658
img Jax MP, Pubmed Id: 20622869, MOUSE PHENOTYPE ID: MGI:1929871
img Jax MP, Pubmed Id: 21743440, MOUSE PHENOTYPE ID: MGI:3652039
HumanPOT125913protection of telomeres 1
INFERRED
HumanSTAG110274stromal antigen 1
img Jax MP, Pubmed Id: 20622869, MOUSE PHENOTYPE ID: MGI:1929871
img Jax MP, Pubmed Id: 21743440, MOUSE PHENOTYPE ID: MGI:3652039
img Jax MP, Pubmed Id: 22415365, MOUSE PHENOTYPE ID: MGI:1098658
img Jax MP, Pubmed Id: 22415365, MOUSE PHENOTYPE ID: MGI:1098658
img Jax MP, Pubmed Id: 20622869, MOUSE PHENOTYPE ID: MGI:1926776
HumanTERT7015telomerase reverse transcriptase
INFERRED
HumanTERF17013telomeric repeat binding factor (NIMA-interacting) 1
INFERRED
HumanPTEN5728phosphatase and tensin homolog
INFERRED
HumanPMS25395PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
INFERRED
HumanFANCC2176Fanconi anemia, complementation group C
INFERRED
HumanDKC11736dyskeratosis congenita 1, dyskerin
INFERRED
HumanCDKN2A1029cyclin-dependent kinase inhibitor 2A
INFERRED
HumanCDK71022cyclin-dependent kinase 7
INFERRED
HumanBRCA1672breast cancer 1, early onset
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010207abnormal telomere morphology0self