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Details
Link-It Detail - Jax Mouse Phenotype - abnormal DNA methylation
Debug Stats
  • ### Total Build Time: 91 ms 21.329 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 376 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=6 ms Completed: 6 ms rowSize= 579 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 602 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.564 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=80 ms Completed: 80 ms rowSize= 16.678 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal DNA methylation MP:0008877
Definition (1)
any anomaly in the covalent transfer of a methyl group to either N-6 of adenine or C-5 or N-4 of cytosine of DNA
Parents (1)
img abnormal cell physiology MP:0005621
Children (1)
img abnormal DNA methylation during gametogenesis MP:0008878
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053844img abnormal cell physiology MP:0005621
Genes (32)

Species:
human : 32
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanPLD6201164phospholipase D family, member 6
INFERRED
HumanTET3200424tet methylcytosine dioxygenase 3
Click here to display 60 evidence detail records.
HumanMDGA2161357MAM domain containing glycosylphosphatidylinositol anchor 2
Click here to display 60 evidence detail records.
HumanDPPA2151871developmental pluripotency associated 2
Click here to display 60 evidence detail records.
HumanASZ1136991ankyrin repeat, SAM and basic leucine zipper domain containing 1
INFERRED
HumanZFP42132625ZFP42 zinc finger protein
Click here to display 60 evidence detail records.
HumanTDRD9122402tudor domain containing 9
INFERRED
HumanMAEL84944maelstrom spermatogenic transposon silencer
INFERRED
HumanDMAP155929DNA methyltransferase 1 associated protein 1
Click here to display 60 evidence detail records.
HumanPIWIL255124piwi-like RNA-mediated gene silencing 2
Click here to display 60 evidence detail records.
HumanMOV10L154456Mov10l1, Moloney leukemia virus 10-like 1, homolog (mouse)
INFERRED
HumanMIS18A54069MIS18 kinetochore protein homolog A (S. pombe)
Click here to display 60 evidence detail records.
HumanARID4B51742AT rich interactive domain 4B (RBP1-like)
Click here to display 60 evidence detail records.
HumanUHRF129128ubiquitin-like with PHD and ring finger domains 1
Click here to display 60 evidence detail records.
HumanSMCHD123347structural maintenance of chromosomes flexible hinge domain containing 1
Click here to display 60 evidence detail records.
HumanRAD5010111RAD50 homolog (S. cerevisiae)
Click here to display 60 evidence detail records.
HumanKMT2B9757lysine (K)-specific methyltransferase 2B
Click here to display 60 evidence detail records.
HumanGCM29247glial cells missing homolog 2 (Drosophila)
Click here to display 60 evidence detail records.
HumanMBD48930methyl-CpG binding domain protein 4
Click here to display 60 evidence detail records.
HumanGCM18521glial cells missing homolog 1 (Drosophila)
Click here to display 60 evidence detail records.
HumanEPM2A7957epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
Click here to display 60 evidence detail records.
HumanTDG6996thymine-DNA glycosylase
Click here to display 60 evidence detail records.
HumanSP36670Sp3 transcription factor
Click here to display 60 evidence detail records.
HumanSNRPN6638small nuclear ribonucleoprotein polypeptide N
Click here to display 60 evidence detail records.
HumanRNF46047ring finger protein 4
Click here to display 60 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008877abnormal DNA methylation0self