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Details
Link-It Detail - Jax Mouse Phenotype - abnormal sinoatrial node conduction
Debug Stats
  • ### Total Build Time: 86 ms 20.683 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 398 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 267 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 180 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=15 ms Completed: 15 ms rowSize= 600 bytes
  • CONCEPT_CHILDREN gt=11 ms Completed: 11 ms rowSize= 1.001 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.598 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=48 ms Completed: 48 ms rowSize= 15.355 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.173 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal sinoatrial node conduction MP:0006142
Definition (1)
anomaly in the generation or transfer of electrical impulses that trigger contraction of the atria and ventricles
Synonyms (1)
"sinoatrial node defect" BROAD
Parents (1)
img abnormal impulse conducting system conduction MP:0003137
Children (2)
img sinoatrial block MP:0010520
img abnormal P wave MP:0004070
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053855img abnormal impulse conducting system conduction MP:0003137
Genes (29)

Species:
human : 29
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanHOPX84525HOP homeobox
INFERRED
HumanDOT1L84444DOT1-like histone H3K79 methyltransferase
INFERRED
HumanPOPDC264091popeye domain containing 2
Click here to display 17 evidence detail records.
HumanMYL758498myosin, light chain 7, regulatory
Click here to display 17 evidence detail records.
HumanSLC2A829988solute carrier family 2 (facilitated glucose transporter), member 8
INFERRED
HumanAKAP1011216A kinase (PRKA) anchor protein 10
Click here to display 17 evidence detail records.
HumanBVES11149blood vessel epicardial substance
Click here to display 17 evidence detail records.
HumanGNB510681guanine nucleotide binding protein (G protein), beta 5
Click here to display 17 evidence detail records.
HumanHCN410021hyperpolarization activated cyclic nucleotide-gated potassium channel 4
Click here to display 17 evidence detail records.
HumanNUP1559631nucleoporin 155kDa
INFERRED
HumanKL9365klotho
Click here to display 17 evidence detail records.
HumanCACNA1G8913calcium channel, voltage-dependent, T type, alpha 1G subunit
Click here to display 17 evidence detail records.
HumanTBX56910T-box 5
Click here to display 17 evidence detail records.
HumanSP46671Sp4 transcription factor
INFERRED
HumanSCN5A6331sodium channel, voltage-gated, type V, alpha subunit
Click here to display 17 evidence detail records.
HumanMMP74316matrix metallopeptidase 7 (matrilysin, uterine)
Click here to display 17 evidence detail records.
HumanLMNA4000lamin A/C
INFERRED
HumanKCNQ13784potassium voltage-gated channel, KQT-like subfamily, member 1
INFERRED
HumanIGHMBP23508immunoglobulin mu binding protein 2
INFERRED
HumanIDUA3425iduronidase, alpha-L-
INFERRED
HumanHCCS3052holocytochrome c synthase
INFERRED
HumanGJA52702gap junction protein, alpha 5, 40kDa
INFERRED
HumanGJA12697gap junction protein, alpha 1, 43kDa
INFERRED
HumanDMD1756dystrophin
INFERRED
HumanCXADR1525coxsackie virus and adenovirus receptor
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006142abnormal sinoatrial node conduction0self