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Details
Link-It Detail - Jax Mouse Phenotype - abnormal myotome development
Debug Stats
  • ### Total Build Time: 37 ms 15.873 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= 241 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=2 ms Completed: 2 ms rowSize= 574 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 590 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.558 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=29 ms Completed: 29 ms rowSize= 11.258 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal myotome development MP:0000737
Definition (1)
malformation of or absence of the part of the somite that develops into the musculature
Parents (1)
img abnormal myogenesis MP:0000729
Children (1)
img abnormal dermomyotome development MP:0004206
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img muscle phenotype MP:00053696img abnormal myogenesis MP:0000729
Genes (19)

Species:
human : 19
SpeciesGeneGeneIdGene NameEvidence
HumanMSGN1343930mesogenin 1
Click here to display 36 evidence detail records.
HumanMESP2145873mesoderm posterior 2 homolog (mouse)
INFERRED
HumanDISP184976dispatched homolog 1 (Drosophila)
Click here to display 36 evidence detail records.
HumanWDR1957728WD repeat domain 19
Click here to display 36 evidence detail records.
HumanPDGFC56034platelet derived growth factor C
Click here to display 36 evidence detail records.
HumanRTEL151750regulator of telomere elongation helicase 1
Click here to display 36 evidence detail records.
HumanAPH1A51107APH1A gamma secretase subunit
Click here to display 36 evidence detail records.
HumanDMRT210655doublesex and mab-3 related transcription factor 2
Click here to display 36 evidence detail records.
HumanWNT17471wingless-type MMTV integration site family, member 1
Click here to display 36 evidence detail records.
HumanRBL25934retinoblastoma-like 2 (p130)
Click here to display 36 evidence detail records.
HumanPDGFRA5156platelet-derived growth factor receptor, alpha polypeptide
Click here to display 36 evidence detail records.
HumanPAX35077paired box 3
Click here to display 36 evidence detail records.
HumanPAX15075paired box 1
Click here to display 36 evidence detail records.
HumanMYF64618myogenic factor 6 (herculin)
Click here to display 36 evidence detail records.
HumanMYF54617myogenic factor 5
Click here to display 36 evidence detail records.
HumanMEOX24223mesenchyme homeobox 2
Click here to display 36 evidence detail records.
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
INFERRED
HumanMECOM2122MDS1 and EVI1 complex locus
Click here to display 36 evidence detail records.
HumanPRDM1639PR domain containing 1, with ZNF domain
Click here to display 36 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000737abnormal myotome development0self