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Details
Link-It Detail - Jax Mouse Phenotype - genetic imprinting
Debug Stats
  • ### Total Build Time: 79 ms 20.616 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 364 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 480 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 176 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=7 ms Completed: 7 ms rowSize= 573 bytes
  • CONCEPT_CHILDREN gt=14 ms Completed: 14 ms rowSize= 1.454 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.559 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=47 ms Completed: 47 ms rowSize= 14.747 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.156 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
genetic imprinting MP:0003121
Definition (1)
any anomaly in the process that modulates the frequency, rate or extent of the chemical reactions and pathways involving macromolecules by a mechanism that is mediated by DNA, is mitotically or meiotically heritable, or is stably self-propagated in the cytoplasm of a resting cell, and does not entail a change in DNA sequence
Synonyms (1)
"genomic imprinting" EXACT
Parents (1)
img cellular phenotype MP:0005384
Children (3)
img maternal imprinting MP:0003122
img abnormal imprinting MP:0003787
img paternal imprinting MP:0003123
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053843img cellular phenotype MP:0005384
Genes (38)

Species:
human : 38
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanZFP57346171ZFP57 zinc finger protein
INFERRED
HumanZFP42132625ZFP42 zinc finger protein
INFERRED
HumanHDAC855869histone deacetylase 8
Click here to display 19 evidence detail records.
HumanMAGEL254551MAGE-like 2
INFERRED
HumanARID4B51742AT rich interactive domain 4B (RBP1-like)
Click here to display 19 evidence detail records.
HumanSMCHD123347structural maintenance of chromosomes flexible hinge domain containing 1
INFERRED
HumanPEG1023089paternally expressed 10
INFERRED
HumanEHMT210919euchromatic histone-lysine N-methyltransferase 2
INFERRED
HumanPLAC110761placenta-specific 1
INFERRED
HumanKMT2B9757lysine (K)-specific methyltransferase 2B
INFERRED
HumanSGCE8910sarcoglycan, epsilon
INFERRED
HumanDLK18788delta-like 1 homolog (Drosophila)
INFERRED
HumanAXIN18312axin 1
Click here to display 19 evidence detail records.
HumanPHLDA27262pleckstrin homology-like domain, family A, member 2
INFERRED
HumanSNRPN6638small nuclear ribonucleoprotein polypeptide N
Click here to display 19 evidence detail records.
HumanARID4A5926AT rich interactive domain 4A (RBP1-like)
Click here to display 19 evidence detail records.
HumanRB15925retinoblastoma 1
INFERRED
HumanRASGRF15923Ras protein-specific guanine nucleotide-releasing factor 1
INFERRED
HumanPLAGL15325pleiomorphic adenoma gene-like 1
INFERRED
HumanPEG35178paternally expressed 3
INFERRED
HumanNDN4692necdin, melanoma antigen (MAGE) family member
INFERRED
HumanCITED14435Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 1
INFERRED
HumanMEST4232mesoderm specific transcript
INFERRED
HumanMEOX24223mesenchyme homeobox 2
INFERRED
HumanIGF2R3482insulin-like growth factor 2 receptor
Click here to display 19 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003121genetic imprinting0self