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Details
Link-It Detail - Jax Mouse Phenotype - absent cochlear nerve compound action potential
Debug Stats
  • ### Total Build Time: 21 ms 27.977 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 422 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= 207 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=3 ms Completed: 3 ms rowSize= 604 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 2.963 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 22.212 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.185 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
absent cochlear nerve compound action potential MP:0004416
Definition (1)
absence of the combined potentials resulting from activation of the auditory division of the eighth cranial nerve
Synonyms (1)
"absent auditory nerve compound action potential" RELATED
Parents (1)
img abnormal cochlear nerve compound action potential MP:0004415
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img abnormal cochlear nerve compound action potential MP:0004415
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal cochlear nerve compound action potential MP:0004415
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
img Jax MP, Pubmed Id: 12036291, MOUSE PHENOTYPE ID: MGI:98364
img Jax MP, Pubmed Id: 7493015, MOUSE PHENOTYPE ID: MGI:104785
img Jax MP, Pubmed Id: 19363478, MOUSE PHENOTYPE ID: MGI:3619440
img Jax MP, Pubmed Id: 9183385, MOUSE PHENOTYPE ID: MGI:107756
img Jax MP, Pubmed Id: 18674745, MOUSE PHENOTYPE ID: MGI:3039629
img Jax MP, Pubmed Id: 12036291, MOUSE PHENOTYPE ID: MGI:98364
img Jax MP, Pubmed Id: 6871029, MOUSE PHENOTYPE ID: MGI:1861630
HumanESPN83715espin
img Jax MP, Pubmed Id: 6871029, MOUSE PHENOTYPE ID: MGI:1861630
img Jax MP, Pubmed Id: 12036291, MOUSE PHENOTYPE ID: MGI:98364
img Jax MP, Pubmed Id: 7493015, MOUSE PHENOTYPE ID: MGI:104785
img Jax MP, Pubmed Id: 19363478, MOUSE PHENOTYPE ID: MGI:3619440
img Jax MP, Pubmed Id: 18674745, MOUSE PHENOTYPE ID: MGI:3039629
img Jax MP, Pubmed Id: 9183385, MOUSE PHENOTYPE ID: MGI:107756
img Jax MP, Pubmed Id: 12036291, MOUSE PHENOTYPE ID: MGI:98364
HumanSOX26657SRY (sex determining region Y)-box 2
img Jax MP, Pubmed Id: 19363478, MOUSE PHENOTYPE ID: MGI:3619440
img Jax MP, Pubmed Id: 12036291, MOUSE PHENOTYPE ID: MGI:98364
img Jax MP, Pubmed Id: 18674745, MOUSE PHENOTYPE ID: MGI:3039629
img Jax MP, Pubmed Id: 6871029, MOUSE PHENOTYPE ID: MGI:1861630
img Jax MP, Pubmed Id: 7493015, MOUSE PHENOTYPE ID: MGI:104785
img Jax MP, Pubmed Id: 12036291, MOUSE PHENOTYPE ID: MGI:98364
img Jax MP, Pubmed Id: 9183385, MOUSE PHENOTYPE ID: MGI:107756
HumanMYO64646myosin VI
img Jax MP, Pubmed Id: 12036291, MOUSE PHENOTYPE ID: MGI:98364
img Jax MP, Pubmed Id: 9183385, MOUSE PHENOTYPE ID: MGI:107756
img Jax MP, Pubmed Id: 19363478, MOUSE PHENOTYPE ID: MGI:3619440
img Jax MP, Pubmed Id: 18674745, MOUSE PHENOTYPE ID: MGI:3039629
img Jax MP, Pubmed Id: 7493015, MOUSE PHENOTYPE ID: MGI:104785
img Jax MP, Pubmed Id: 12036291, MOUSE PHENOTYPE ID: MGI:98364
img Jax MP, Pubmed Id: 6871029, MOUSE PHENOTYPE ID: MGI:1861630
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004416absent cochlear nerve compound action potential0self