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Details
Link-It Detail - Jax Mouse Phenotype - abnormal heart electrocardiography waveform feature
Debug Stats
  • ### Total Build Time: 26 ms 24.760 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 430 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 196 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 600 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 5.458 KB
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  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 14.694 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.188 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal heart electrocardiography waveform feature MP:0010508
Definition (1)
any anomaly in the pattern of the graphic record of the integrated action currents of the cardiac cycle represented as changes in voltage; the prominent waves in the ECG correspond to specific conduction activity in areas of the heart and the timing and amplitude of ECG waveforms provide valuable information about heart rate and rhythm
Synonyms (1)
"abnormal heart ECG waveform features" RELATED
Parents (1)
img abnormal impulse conducting system conduction MP:0003137
Children (12)
img abnormal ST segment MP:0003897
img abnormal T wave MP:0010505
img abnormal QT interval MP:0003899
img abnormal HV interval MP:0010552
img abnormal PR interval MP:0003901
img abnormal QRS complex MP:0003898
img abnormal RR interval MP:0010504
img abnormal R wave MP:0011919
img abnormal S wave MP:0011920
img abnormal PP interval MP:0011936
img abnormal P wave MP:0004070
img abnormal PQ interval MP:0011918
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053855img abnormal impulse conducting system conduction MP:0003137
Genes (66)

Species:
human : 66
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanXIRP1165904xin actin-binding repeat containing 1
INFERRED
HumanGJD3125111gap junction protein, delta 3, 31.9kDa
INFERRED
HumanFOXP293986forkhead box P2
INFERRED
HumanHOPX84525HOP homeobox
INFERRED
HumanDOT1L84444DOT1-like histone H3K79 methyltransferase
INFERRED
HumanIRX379191iroquois homeobox 3
Click here to display 23 evidence detail records.
HumanHCN357657hyperpolarization activated cyclic nucleotide-gated potassium channel 3
INFERRED
HumanSCN3B55800sodium channel, voltage-gated, type III, beta subunit
Click here to display 23 evidence detail records.
HumanDGCR854487DGCR8 microprocessor complex subunit
INFERRED
HumanSLC2A829988solute carrier family 2 (facilitated glucose transporter), member 8
INFERRED
HumanDLL128514delta-like 1 (Drosophila)
INFERRED
HumanSYNE123345spectrin repeat containing, nuclear envelope 1
INFERRED
HumanAKAP1011216A kinase (PRKA) anchor protein 10
INFERRED
HumanABCC910060ATP-binding cassette, sub-family C (CFTR/MRP), member 9
INFERRED
HumanHCN410021hyperpolarization activated cyclic nucleotide-gated potassium channel 4
INFERRED
HumanNUP1559631nucleoporin 155kDa
INFERRED
HumanATG59474autophagy related 5
INFERRED
HumanKL9365klotho
INFERRED
HumanCACNA1G8913calcium channel, voltage-dependent, T type, alpha 1G subunit
INFERRED
HumanVEGFA7422vascular endothelial growth factor A
INFERRED
HumanVCL7414vinculin
Click here to display 23 evidence detail records.
HumanTNNT27139troponin T type 2 (cardiac)
Click here to display 23 evidence detail records.
HumanTHRA7067thyroid hormone receptor, alpha
INFERRED
HumanTH7054tyrosine hydroxylase
INFERRED
HumanTBX56910T-box 5
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010508abnormal heart electrocardiography waveform feature0self