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Details
Link-It Detail - Jax Mouse Phenotype - cardiomyopathy
Debug Stats
  • ### Total Build Time: 337 ms 22.863 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 356 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 217 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=9 ms Completed: 9 ms rowSize= 1.034 KB
  • CONCEPT_CHILDREN gt=8 ms Completed: 8 ms rowSize= 1.018 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.924 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=306 ms Completed: 306 ms rowSize= 16.031 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
cardiomyopathy MP:0005330
Definition (1)
diseases of the heart (myocardium); may result from many causes
Parents (2)
img abnormal muscle physiology MP:0002106
img abnormal cardiovascular system physiology MP:0001544
Children (2)
img ventricular cardiomyopathy MP:0002952
img dilated cardiomyopathy MP:0002795
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img muscle phenotype MP:00053694img abnormal muscle physiology MP:0002106
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053854img abnormal cardiovascular system physiology MP:0001544
Genes (95)

Species:
human : 95
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMTERFD2130916MTERF domain containing 2
Click here to display 78 evidence detail records.
HumanFNIP196459folliculin interacting protein 1
Click here to display 78 evidence detail records.
HumanDOT1L84444DOT1-like histone H3K79 methyltransferase
INFERRED
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
INFERRED
HumanMYH1479784myosin, heavy chain 14, non-muscle
Click here to display 78 evidence detail records.
HumanABCG564240ATP-binding cassette, sub-family G (WHITE), member 5
Click here to display 78 evidence detail records.
HumanMCOLN157192mucolipin 1
INFERRED
HumanTRIM5457159tripartite motif containing 54
INFERRED
HumanTBX2057057T-box 20
INFERRED
HumanEGLN154583egl-9 family hypoxia-inducible factor 1
Click here to display 78 evidence detail records.
HumanMYOZ251778myozenin 2
Click here to display 78 evidence detail records.
HumanSIRT751547sirtuin 7
Click here to display 78 evidence detail records.
HumanMTERFD151001MTERF domain containing 1
Click here to display 78 evidence detail records.
HumanIRX450805iroquois homeobox 4
Click here to display 78 evidence detail records.
HumanKLF1528999Kruppel-like factor 15
Click here to display 78 evidence detail records.
HumanHEY223493hairy/enhancer-of-split related with YRPW motif 2
Click here to display 78 evidence detail records.
HumanABCA523461ATP-binding cassette, sub-family A (ABC1), member 5
INFERRED
HumanSTAB123166stabilin 1
INFERRED
HumanTREX111277three prime repair exonuclease 1
Click here to display 78 evidence detail records.
HumanABCB811194ATP-binding cassette, sub-family B (MDR/TAP), member 8
Click here to display 78 evidence detail records.
HumanPPP1R13L10848protein phosphatase 1, regulatory subunit 13 like
INFERRED
HumanHEXIM110614hexamethylene bis-acetamide inducible 1
INFERRED
HumanPDLIM510611PDZ and LIM domain 5
INFERRED
HumanZMPSTE2410269zinc metallopeptidase STE24
INFERRED
HumanRCE19986RCE1 homolog, prenyl protein protease (S. cerevisiae)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005330cardiomyopathy0self