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Details
Link-It Detail - Jax Mouse Phenotype - abnormal atrioventricular node conduction
Debug Stats
  • ### Total Build Time: 77 ms 41.515 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 410 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 284 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 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=0 Completed: 0 ms rowSize= 600 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 1.012 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=57 ms Completed: 57 ms rowSize= 36.137 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.179 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal atrioventricular node conduction MP:0006141
Definition (1)
anomaly in the generation or transfer of cardiac electrical impulses from the atrioventricular node to the atrioventricular bundle
Synonyms (1)
"atrioventricular node defect" EXACT
Parents (1)
img abnormal impulse conducting system conduction MP:0003137
Children (2)
img abnormal PR interval MP:0003901
img atrioventricular block MP:0010519
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053855img abnormal impulse conducting system conduction MP:0003137
Genes (39)

Species:
human : 39
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGJD3125111gap junction protein, delta 3, 31.9kDa
img Jax MP, Pubmed Id: 16571663, MOUSE PHENOTYPE ID: MGI:2384150
img Jax MP, Pubmed Id: 18794341, MOUSE PHENOTYPE ID: MGI:1201679
img Jax MP, Pubmed Id: 15289437, MOUSE PHENOTYPE ID: MGI:102541
img Jax MP, Pubmed Id: 18084293, MOUSE PHENOTYPE ID: MGI:3813453
img Jax MP, Pubmed Id: 18084293, MOUSE PHENOTYPE ID: MGI:3813453
img Jax MP, Pubmed Id: 15923312, MOUSE PHENOTYPE ID: MGI:4450975
img Jax MP, Pubmed Id: 17224479, MOUSE PHENOTYPE ID: MGI:1914186
img Jax MP, Pubmed Id: 16690884, MOUSE PHENOTYPE ID: MGI:1201678
img Jax MP, Pubmed Id: 10021468, MOUSE PHENOTYPE ID: MGI:94906
img Jax MP, Pubmed Id: 12016261, MOUSE PHENOTYPE ID: MGI:4450975
HumanDOT1L84444DOT1-like histone H3K79 methyltransferase
INFERRED
HumanIRX379191iroquois homeobox 3
INFERRED
HumanSLC30A564924solute carrier family 30 (zinc transporter), member 5
INFERRED
HumanDGCR854487DGCR8 microprocessor complex subunit
INFERRED
HumanSYNE123345spectrin repeat containing, nuclear envelope 1
INFERRED
HumanAKAP1011216A kinase (PRKA) anchor protein 10
INFERRED
HumanHCN410021hyperpolarization activated cyclic nucleotide-gated potassium channel 4
INFERRED
HumanCACNA1G8913calcium channel, voltage-dependent, T type, alpha 1G subunit
img Jax MP, Pubmed Id: 12016261, MOUSE PHENOTYPE ID: MGI:4450975
img Jax MP, Pubmed Id: 10021468, MOUSE PHENOTYPE ID: MGI:94906
img Jax MP, Pubmed Id: 16571663, MOUSE PHENOTYPE ID: MGI:2384150
img Jax MP, Pubmed Id: 15289437, MOUSE PHENOTYPE ID: MGI:102541
img Jax MP, Pubmed Id: 16690884, MOUSE PHENOTYPE ID: MGI:1201678
img Jax MP, Pubmed Id: 18794341, MOUSE PHENOTYPE ID: MGI:1201679
img Jax MP, Pubmed Id: 18084293, MOUSE PHENOTYPE ID: MGI:3813453
img Jax MP, Pubmed Id: 17224479, MOUSE PHENOTYPE ID: MGI:1914186
img Jax MP, Pubmed Id: 15923312, MOUSE PHENOTYPE ID: MGI:4450975
img Jax MP, Pubmed Id: 18084293, MOUSE PHENOTYPE ID: MGI:3813453
HumanTBX56910T-box 5
img Jax MP, Pubmed Id: 17224479, MOUSE PHENOTYPE ID: MGI:1914186
img Jax MP, Pubmed Id: 18084293, MOUSE PHENOTYPE ID: MGI:3813453
img Jax MP, Pubmed Id: 16571663, MOUSE PHENOTYPE ID: MGI:2384150
img Jax MP, Pubmed Id: 15289437, MOUSE PHENOTYPE ID: MGI:102541
img Jax MP, Pubmed Id: 12016261, MOUSE PHENOTYPE ID: MGI:4450975
img Jax MP, Pubmed Id: 16690884, MOUSE PHENOTYPE ID: MGI:1201678
img Jax MP, Pubmed Id: 10021468, MOUSE PHENOTYPE ID: MGI:94906
img Jax MP, Pubmed Id: 18084293, MOUSE PHENOTYPE ID: MGI:3813453
img Jax MP, Pubmed Id: 15923312, MOUSE PHENOTYPE ID: MGI:4450975
img Jax MP, Pubmed Id: 18794341, MOUSE PHENOTYPE ID: MGI:1201679
HumanSP46671Sp4 transcription factor
INFERRED
HumanSMN26607survival of motor neuron 2, centromeric
INFERRED
HumanSMN16606survival of motor neuron 1, telomeric
INFERRED
HumanSCN5A6331sodium channel, voltage-gated, type V, alpha subunit
INFERRED
HumanRXRA6256retinoid X receptor, alpha
INFERRED
HumanMYL24633myosin, light chain 2, regulatory, cardiac, slow
INFERRED
HumanMMP74316matrix metallopeptidase 7 (matrilysin, uterine)
INFERRED
HumanLMNA4000lamin A/C
INFERRED
HumanKCNQ13784potassium voltage-gated channel, KQT-like subfamily, member 1
INFERRED
HumanKCNA13736potassium voltage-gated channel, shaker-related subfamily, member 1 (episodic ataxia with myokymia)
INFERRED
HumanIGHMBP23508immunoglobulin mu binding protein 2
INFERRED
HumanHLA-DQB13119
INFERRED
HumanMNX13110motor neuron and pancreas homeobox 1
INFERRED
HumanHCCS3052holocytochrome c synthase
INFERRED
HumanHADHB3032hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase/enoyl-CoA hydratase (trifunctional protein), beta subunit
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006141abnormal atrioventricular node conduction0self