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Details
Link-It Detail - Jax Mouse Phenotype - abnormal P wave
Debug Stats
  • ### Total Build Time: 17 ms 23.909 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 358 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 410 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=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 1.053 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.452 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.957 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 16.399 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.153 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal P wave MP:0004070
Definition (1)
any anomaly in the P wave which represents atrial depolarization and corresponds to electrical impulses rather than mechanical atria contractions; irregular or absent P waves may indicate arrhythmia and the shape of the P waves may indicate atrial problems
Parents (2)
img abnormal heart electrocardiography waveform feature MP:0010508
img abnormal sinoatrial node conduction MP:0006142
Children (3)
img decreased P wave amplitude MP:0010509
img absent P wave MP:0010510
img prolonged P wave MP:0004071
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053856img abnormal heart electrocardiography waveform feature MP:0010508
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053856img abnormal sinoatrial node conduction MP:0006142
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanHOPX84525HOP homeobox
INFERRED
HumanDOT1L84444DOT1-like histone H3K79 methyltransferase
INFERRED
HumanSLC2A829988solute carrier family 2 (facilitated glucose transporter), member 8
INFERRED
HumanAKAP1011216A kinase (PRKA) anchor protein 10
img Jax MP, Pubmed Id: 22912742, MOUSE PHENOTYPE ID: MGI:5461576
img Jax MP, Pubmed Id: 11226272, MOUSE PHENOTYPE ID: MGI:108083
img Jax MP, Pubmed Id: 15317754, MOUSE PHENOTYPE ID: MGI:3054421
img Jax MP, Pubmed Id: 21880664, MOUSE PHENOTYPE ID: MGI:2447636
img Jax MP, Pubmed Id: 17485678, MOUSE PHENOTYPE ID: MGI:1890218
img Jax MP, Pubmed Id: 11901182, MOUSE PHENOTYPE ID: MGI:2665552
HumanNUP1559631nucleoporin 155kDa
INFERRED
HumanTBX56910T-box 5
INFERRED
HumanSCN5A6331sodium channel, voltage-gated, type V, alpha subunit
INFERRED
HumanKCNQ13784potassium voltage-gated channel, KQT-like subfamily, member 1
img Jax MP, Pubmed Id: 17485678, MOUSE PHENOTYPE ID: MGI:1890218
img Jax MP, Pubmed Id: 11901182, MOUSE PHENOTYPE ID: MGI:2665552
img Jax MP, Pubmed Id: 11226272, MOUSE PHENOTYPE ID: MGI:108083
img Jax MP, Pubmed Id: 21880664, MOUSE PHENOTYPE ID: MGI:2447636
img Jax MP, Pubmed Id: 15317754, MOUSE PHENOTYPE ID: MGI:3054421
img Jax MP, Pubmed Id: 22912742, MOUSE PHENOTYPE ID: MGI:5461576
HumanIGHMBP23508immunoglobulin mu binding protein 2
INFERRED
HumanIDUA3425iduronidase, alpha-L-
INFERRED
HumanGJA52702gap junction protein, alpha 5, 40kDa
INFERRED
HumanGJA12697gap junction protein, alpha 1, 43kDa
INFERRED
HumanDMD1756dystrophin
INFERRED
HumanCXADR1525coxsackie virus and adenovirus receptor
INFERRED
HumanCENPF1063centromere protein F, 350/400kDa
INFERRED
HumanCDC42998cell division cycle 42
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004070abnormal P wave0self