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Details
Link-It Detail - Jax Mouse Phenotype - impaired muscle contractility
Debug Stats
  • ### Total Build Time: 136 ms 20.287 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 237 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=7 ms Completed: 7 ms rowSize= 584 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.508 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.567 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=103 ms Completed: 103 ms rowSize= 14.722 KB
  • CONCEPT_XREFS gt=8 ms Completed: 8 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
impaired muscle contractility MP:0000738
Definition (1)
inability or reduced ability of a muscle to shorten or to develop increased tension
Parents (1)
img abnormal muscle contractility MP:0005620
Children (3)
img impaired skeletal muscle contractility MP:0002841
img decreased cardiac muscle contractility MP:0005140
img impaired smooth muscle contractility MP:0000740
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img muscle phenotype MP:00053695img abnormal muscle contractility MP:0005620
Genes (223)

Species:
human : 223
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanTRIM72493829tripartite motif containing 72
INFERRED
HumanPLIN5440503perilipin 5
INFERRED
HumanKY339855kyphoscoliosis peptidase
INFERRED
HumanSYPL2284612synaptophysin-like 2
INFERRED
HumanSMTNL1219537smoothelin-like 1
INFERRED
HumanXIRP1165904xin actin-binding repeat containing 1
INFERRED
HumanMYLK391807myosin light chain kinase 3
INFERRED
HumanMYLK285366myosin light chain kinase 2
INFERRED
HumanTRIM6384676tripartite motif containing 63, E3 ubiquitin protein ligase
INFERRED
HumanHOPX84525HOP homeobox
INFERRED
HumanSYNC81493syncoilin, intermediate filament protein
INFERRED
HumanMTMR1464419myotubularin related protein 14
INFERRED
HumanACE259272angiotensin I converting enzyme 2
INFERRED
HumanHEG157493heart development protein with EGF-like domains 1
INFERRED
HumanPNPLA257104patatin-like phospholipase domain containing 2
INFERRED
HumanTBX2057057T-box 20
INFERRED
HumanJPH156704junctophilin 1
INFERRED
HumanSULF255959sulfatase 2
INFERRED
HumanLIMS255679LIM and senescent cell antigen-like domains 2
INFERRED
HumanEGLN154583egl-9 family hypoxia-inducible factor 1
INFERRED
HumanDGCR854487DGCR8 microprocessor complex subunit
INFERRED
HumanMYOZ251778myozenin 2
INFERRED
HumanPLCE151196phospholipase C, epsilon 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000738impaired muscle contractility0self