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Details
Link-It Detail - Jax Mouse Phenotype - skeletal muscle fiber degeneration
Debug Stats
  • ### Total Build Time: 35 ms 15.131 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 251 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=4 ms Completed: 4 ms rowSize= 1.036 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 2.911 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=20 ms Completed: 20 ms rowSize= 9.228 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
skeletal muscle fiber degeneration MP:0009412
Definition (1)
pathological deterioration of skeletal muscle fiber tissue, often accompanied by loss of function
Parents (2)
img skeletal muscle degeneration MP:0009415
img abnormal skeletal muscle fiber morphology MP:0003084
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img muscle phenotype MP:00053696img skeletal muscle degeneration MP:0009415
img mammalian phenotype MP:0000001img muscle phenotype MP:00053696img abnormal skeletal muscle fiber morphology MP:0003084
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanFKRP79147fukutin related protein
Click here to display 25 evidence detail records.
HumanMYOF26509myoferlin
Click here to display 25 evidence detail records.
HumanBAG39531BCL2-associated athanogene 3
Click here to display 25 evidence detail records.
HumanLARGE9215like-glycosyltransferase
Click here to display 25 evidence detail records.
HumanDYSF8291dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive)
Click here to display 25 evidence detail records.
HumanSMN26607survival of motor neuron 2, centromeric
Click here to display 25 evidence detail records.
HumanSMN16606survival of motor neuron 1, telomeric
Click here to display 25 evidence detail records.
HumanSGCB6443sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
Click here to display 25 evidence detail records.
HumanPRKDC5591protein kinase, DNA-activated, catalytic polypeptide
Click here to display 25 evidence detail records.
HumanPFKM5213phosphofructokinase, muscle
Click here to display 25 evidence detail records.
HumanMYH44622myosin, heavy chain 4, skeletal muscle
Click here to display 25 evidence detail records.
HumanMTOR2475mechanistic target of rapamycin (serine/threonine kinase)
Click here to display 25 evidence detail records.
HumanDUSP11843dual specificity phosphatase 1
Click here to display 25 evidence detail records.
HumanDMD1756dystrophin
Click here to display 25 evidence detail records.
HumanCFL21073cofilin 2 (muscle)
Click here to display 25 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009412skeletal muscle fiber degeneration0self