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Details
Link-It Detail - Jax Mouse Phenotype - muscle degeneration
Debug Stats
  • ### Total Build Time: 86 ms 20.808 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 366 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • 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=4 ms Completed: 4 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.024 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.564 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=73 ms Completed: 73 ms rowSize= 15.762 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
muscle degeneration MP:0000749
Definition (1)
pathological deterioration of muscle tissue, often accompanied by loss of function
Parents (1)
img abnormal muscle morphology MP:0002108
Children (2)
img skeletal muscle degeneration MP:0009415
img cardiac muscle degeneration MP:0009416
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img muscle phenotype MP:00053694img abnormal muscle morphology MP:0002108
Genes (49)

Species:
human : 49
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Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCISD2493856CDGSH iron sulfur domain 2
Click here to display 54 evidence detail records.
HumanKY339855kyphoscoliosis peptidase
Click here to display 54 evidence detail records.
HumanMAMSTR284358MEF2 activating motif and SAP domain containing transcriptional regulator
Click here to display 54 evidence detail records.
HumanFKRP79147fukutin related protein
INFERRED
HumanMYOZ158529myozenin 1
Click here to display 54 evidence detail records.
HumanPIK3R430849phosphoinositide-3-kinase, regulatory subunit 4
INFERRED
HumanMYOF26509myoferlin
INFERRED
HumanBAG39531BCL2-associated athanogene 3
INFERRED
HumanLARGE9215like-glycosyltransferase
Click here to display 54 evidence detail records.
HumanBUB39184BUB3 mitotic checkpoint protein
Click here to display 54 evidence detail records.
HumanAIFM19131apoptosis-inducing factor, mitochondrion-associated, 1
Click here to display 54 evidence detail records.
HumanDYSF8291dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive)
INFERRED
HumanUTRN7402utrophin
Click here to display 54 evidence detail records.
HumanSMN26607survival of motor neuron 2, centromeric
INFERRED
HumanSMN16606survival of motor neuron 1, telomeric
INFERRED
HumanSGCG6445sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
Click here to display 54 evidence detail records.
HumanSGCD6444sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
Click here to display 54 evidence detail records.
HumanSGCB6443sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
INFERRED
HumanSCN8A6334sodium channel, voltage gated, type VIII, alpha subunit
Click here to display 54 evidence detail records.
HumanATXN16310ataxin 1
Click here to display 54 evidence detail records.
HumanRYR16261ryanodine receptor 1 (skeletal)
INFERRED
HumanPRKDC5591protein kinase, DNA-activated, catalytic polypeptide
INFERRED
HumanPMP225376peripheral myelin protein 22
Click here to display 54 evidence detail records.
HumanPLEC5339plectin
Click here to display 54 evidence detail records.
HumanPFKM5213phosphofructokinase, muscle
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000749muscle degeneration0self