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Details
Link-It Detail - Jax Mouse Phenotype - embryonic growth retardation
Debug Stats
  • ### Total Build Time: 18,427 ms 26.105 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 384 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 268 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 187 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= 1.498 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.268 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18,414 ms Completed: 18.414 Seconds rowSize= 18.202 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
embryonic growth retardation MP:0003984
Definition (1)
slow or limited development during the embryonic period (sensu Mus: up to E14, or the completion of organogenesis)
Synonyms (1)
"delayed embryonic development" EXACT
Parents (3)
img prenatal growth retardation MP:0010865
img abnormal embryogenesis/ development MP:0001672
img abnormal embryonic growth/weight/body size MP:0002088
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img growth/size phenotype MP:00053785img prenatal growth retardation MP:0010865
img mammalian phenotype MP:0000001img embryogenesis phenotype MP:00053804img abnormal embryogenesis/ development MP:0001672
img mammalian phenotype MP:0000001img growth/size phenotype MP:00053785img abnormal embryonic growth/weight/body size MP:0002088
Genes (422)

Species:
human : 422
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanSCXA100129885scleraxis homolog A (mouse)
Click here to display 698 evidence detail records.
HumanSCXB642658scleraxis homolog B (mouse)
Click here to display 698 evidence detail records.
HumanDPH3285381diphthamide biosynthesis 3
Click here to display 698 evidence detail records.
HumanLAMA1284217laminin, alpha 1
Click here to display 698 evidence detail records.
HumanIPMK253430inositol polyphosphate multikinase
Click here to display 698 evidence detail records.
HumanRICTOR253260RPTOR independent companion of MTOR, complex 2
Click here to display 698 evidence detail records.
HumanPKD1L1168507polycystic kidney disease 1 like 1
Click here to display 698 evidence detail records.
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
Click here to display 698 evidence detail records.
HumanAMOT154796angiomotin
Click here to display 698 evidence detail records.
HumanCOMMD1150684copper metabolism (Murr1) domain containing 1
Click here to display 698 evidence detail records.
HumanSMYD1150572SET and MYND domain containing 1
Click here to display 698 evidence detail records.
HumanTTBK2146057tau tubulin kinase 2
Click here to display 698 evidence detail records.
HumanRAD9B144715RAD9 homolog B (S. pombe)
Click here to display 698 evidence detail records.
HumanE2F7144455E2F transcription factor 7
Click here to display 698 evidence detail records.
HumanPTPMT1114971protein tyrosine phosphatase, mitochondrial 1
Click here to display 698 evidence detail records.
HumanMYOCD93649myocardin
Click here to display 698 evidence detail records.
HumanGADD45GIP190480growth arrest and DNA-damage-inducible, gamma interacting protein 1
Click here to display 698 evidence detail records.
HumanDOT1L84444DOT1-like histone H3K79 methyltransferase
Click here to display 698 evidence detail records.
HumanNOA184273nitric oxide associated 1
Click here to display 698 evidence detail records.
HumanATAD3B83858ATPase family, AAA domain containing 3B
Click here to display 698 evidence detail records.
HumanCCM283605cerebral cavernous malformation 2
Click here to display 698 evidence detail records.
HumanSOX783595SRY (sex determining region Y)-box 7
Click here to display 698 evidence detail records.
HumanTET180312tet methylcytosine dioxygenase 1
Click here to display 698 evidence detail records.
HumanGRHL279977grainyhead-like 2 (Drosophila)
Click here to display 698 evidence detail records.
HumanKDM879831lysine (K)-specific demethylase 8
Click here to display 698 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003984embryonic growth retardation0self