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Details
Link-It Detail - Jax Mouse Phenotype - abnormal muscle physiology
Debug Stats
  • ### Total Build Time: 1,317 ms 30.169 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_GENES gt=1,312 ms Completed: 1.312 Seconds rowSize= 15.854 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.164 KB
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Jax Mouse Phenotype (1)
abnormal muscle physiology MP:0002106
Definition (1)
any functional anomaly of the muscle, not due to an anatomical defect
Synonyms (1)
"musculature: physiological defects" EXACT
Parents (1)
img muscle phenotype MP:0005369
Children (22)
img abnormal muscle regeneration MP:0000750
img myositis MP:0004510
img abnormal cardiomyocyte apoptosis MP:0003221
img abnormal fetal cardiomyocyte proliferation MP:0003567
img abnormal muscle cell glucose uptake MP:0004130
img abnormal muscle contractility MP:0005620
img abnormal muscle relaxation MP:0004036
img decreased skeletal muscle glycogen level MP:0010399
img increased muscle free fatty acid level MP:0003249
img abnormal tendon stiffness MP:0003097
img myopathy MP:0000751
img abnormal gastroesophageal sphincter physiology MP:0010154
img muscle fatigue MP:0003646
img abnormal vascular smooth muscle physiology MP:0005595
img abnormal skeletal muscle satellite cell proliferation MP:0009410
img ophthalmoplegia MP:0003689
img cardiomyopathy MP:0005330
img muscle weakness MP:0000747
img abnormal muscle tone MP:0004142
img abnormal muscle electrophysiology MP:0004145
img muscle twitch MP:0009046
img increased skeletal muscle glycogen level MP:0010401
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img muscle phenotype MP:00053693img muscle phenotype MP:0005369
Genes (700)

Species:
human : 700
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanTRIM72493829tripartite motif containing 72
Click here to display 155 evidence detail records.
HumanPLIN5440503perilipin 5
INFERRED
HumanNHLRC1378884NHL repeat containing 1
INFERRED
HumanSLC27A1376497solute carrier family 27 (fatty acid transporter), member 1
INFERRED
HumanHMX3340784H6 family homeobox 3
INFERRED
HumanKY339855kyphoscoliosis peptidase
INFERRED
HumanSYPL2284612synaptophysin-like 2
INFERRED
HumanMAMSTR284358MEF2 activating motif and SAP domain containing transcriptional regulator
Click here to display 155 evidence detail records.
HumanSLC13A5284111solute carrier family 13 (sodium-dependent citrate transporter), member 5
Click here to display 155 evidence detail records.
HumanNPAS4266743neuronal PAS domain protein 4
INFERRED
HumanFOXK1221937forkhead box K1
INFERRED
HumanGJD4219770gap junction protein, delta 4, 40.1kDa
INFERRED
HumanSMTNL1219537smoothelin-like 1
INFERRED
HumanPIKFYVE200576phosphoinositide kinase, FYVE finger containing
INFERRED
HumanARX170302aristaless related homeobox
INFERRED
HumanXIRP1165904xin actin-binding repeat containing 1
INFERRED
HumanSLC32A1140679solute carrier family 32 (GABA vesicular transporter), member 1
INFERRED
HumanGATA5140628GATA binding protein 5
INFERRED
HumanPPARGC1B133522peroxisome proliferator-activated receptor gamma, coactivator 1 beta
Click here to display 155 evidence detail records.
HumanMTERFD2130916MTERF domain containing 2
INFERRED
HumanXIRP2129446xin actin-binding repeat containing 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002106abnormal muscle physiology0self