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Details
Link-It Detail - Jax Mouse Phenotype - abnormal imprinting
Debug Stats
  • ### Total Build Time: 54 ms 16.031 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 366 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 1.005 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.897 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=45 ms Completed: 45 ms rowSize= 9.909 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal imprinting MP:0003787
Definition (1)
defects in the establishment of heritable alterations in the activity of a gene that depend on whether it passed through the paternal or the maternal germline, but that are not encoded by DNA itself
Synonyms (1)
"abnormal regulation of gene expression by DNA imprinting" EXACT
Parents (2)
img genetic imprinting MP:0003121
img abnormal metabolism MP:0005266
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053844img genetic imprinting MP:0003121
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053764img abnormal metabolism MP:0005266
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanZFP57346171ZFP57 zinc finger protein
Click here to display 69 evidence detail records.
HumanZFP42132625ZFP42 zinc finger protein
Click here to display 69 evidence detail records.
HumanARID4B51742AT rich interactive domain 4B (RBP1-like)
Click here to display 69 evidence detail records.
HumanSMCHD123347structural maintenance of chromosomes flexible hinge domain containing 1
Click here to display 69 evidence detail records.
HumanEHMT210919euchromatic histone-lysine N-methyltransferase 2
Click here to display 69 evidence detail records.
HumanKMT2B9757lysine (K)-specific methyltransferase 2B
Click here to display 69 evidence detail records.
HumanSNRPN6638small nuclear ribonucleoprotein polypeptide N
Click here to display 69 evidence detail records.
HumanARID4A5926AT rich interactive domain 4A (RBP1-like)
Click here to display 69 evidence detail records.
HumanRB15925retinoblastoma 1
Click here to display 69 evidence detail records.
HumanRASGRF15923Ras protein-specific guanine nucleotide-releasing factor 1
Click here to display 69 evidence detail records.
HumanPEG35178paternally expressed 3
Click here to display 69 evidence detail records.
HumanMEOX24223mesenchyme homeobox 2
Click here to display 69 evidence detail records.
HumanIGF23481insulin-like growth factor 2 (somatomedin A)
Click here to display 69 evidence detail records.
HumanDNMT11786DNA (cytosine-5-)-methyltransferase 1
Click here to display 69 evidence detail records.
HumanCDKN1C1028cyclin-dependent kinase inhibitor 1C (p57, Kip2)
Click here to display 69 evidence detail records.
HumanATRX546alpha thalassemia/mental retardation syndrome X-linked
Click here to display 69 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003787abnormal imprinting0self