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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vocalization
Debug Stats
  • ### Total Build Time: 71 ms 21.104 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 370 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 311 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= 572 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.570 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=66 ms Completed: 66 ms rowSize= 16.999 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal vocalization MP:0001529
Definition (1)
an inability, decreased ability or altered ability to produce sound from the vocal organs; or a general increase or decrease in the production of vocal sound
Parents (1)
img abnormal behavior MP:0004924
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053864img abnormal behavior MP:0004924
Genes (30)

Species:
human : 30
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanFOXP293986forkhead box P2
Click here to display 66 evidence detail records.
HumanCELF660677CUGBP, Elav-like family member 6
Click here to display 66 evidence detail records.
HumanNLGN354413neuroligin 3
Click here to display 66 evidence detail records.
HumanCNTNAP226047contactin associated protein-like 2
Click here to display 66 evidence detail records.
HumanSHANK222941SH3 and multiple ankyrin repeat domains 2
Click here to display 66 evidence detail records.
HumanGPHN10243gephyrin
Click here to display 66 evidence detail records.
HumanGTF2IRD19569GTF2I repeat domain containing 1
Click here to display 66 evidence detail records.
HumanMKKS8195McKusick-Kaufman syndrome
Click here to display 66 evidence detail records.
HumanFZD37976frizzled family receptor 3
Click here to display 66 evidence detail records.
HumanWFS17466Wolfram syndrome 1 (wolframin)
Click here to display 66 evidence detail records.
HumanTBX16899T-box 1
Click here to display 66 evidence detail records.
HumanTACR16869tachykinin receptor 1
Click here to display 66 evidence detail records.
HumanMAPK65597mitogen-activated protein kinase 6
Click here to display 66 evidence detail records.
HumanPLP15354proteolipid protein 1
Click here to display 66 evidence detail records.
HumanOXTR5021oxytocin receptor
Click here to display 66 evidence detail records.
HumanNDUFS44724NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
Click here to display 66 evidence detail records.
HumanMTM14534myotubularin 1
Click here to display 66 evidence detail records.
HumanLMX1B4010LIM homeobox transcription factor 1, beta
Click here to display 66 evidence detail records.
HumanFMR12332fragile X mental retardation 1
Click here to display 66 evidence detail records.
HumanE2F41874E2F transcription factor 4, p107/p130-binding
Click here to display 66 evidence detail records.
HumanTOR1A1861torsin family 1, member A (torsin A)
Click here to display 66 evidence detail records.
HumanDRD21813dopamine receptor D2
Click here to display 66 evidence detail records.
HumanDLG41742discs, large homolog 4 (Drosophila)
Click here to display 66 evidence detail records.
HumanDHCR717177-dehydrocholesterol reductase
Click here to display 66 evidence detail records.
HumanCHRNE1145cholinergic receptor, nicotinic, epsilon (muscle)
Click here to display 66 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001529abnormal vocalization0self