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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vestibular ganglion morphology
Debug Stats
  • ### Total Build Time: 110 ms 21.735 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 406 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 299 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 224 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=13 ms Completed: 13 ms rowSize= 590 bytes
  • CONCEPT_CHILDREN gt=13 ms Completed: 13 ms rowSize= 1.951 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=21 ms Completed: 21 ms rowSize= 1.581 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=50 ms Completed: 50 ms rowSize= 15.398 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.177 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal vestibular ganglion morphology MP:0002856
Definition (1)
any structural anomaly of the group of neurons associated with the vestibular part of the eighth cranial nerve that are involved in equilibration
Synonyms (1)
"abnormal vestibular ganglion of the vestibulocochlear (VIII) nerve" EXACT
Parents (1)
img abnormal cranial ganglia morphology MP:0001081
Children (4)
img absent vestibular ganglion MP:0004299
img small vestibular ganglion MP:0003987
img vestibular ganglion degeneration MP:0004298
img abnormal pars superior vestibularis morphology MP:0000028
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal cranial ganglia morphology MP:0001081
Genes (26)

Species:
human : 26
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 17 evidence detail records.
HumanTBX10347853T-box 10
INFERRED
HumanOTOP1133060otopetrin 1
Click here to display 17 evidence detail records.
HumanSLITRK684189SLIT and NTRK-like family, member 6
INFERRED
HumanSCUBE180274signal peptide, CUB domain, EGF-like 1
Click here to display 17 evidence detail records.
HumanVTI1B10490vesicle transport through interaction with t-SNAREs 1B
INFERRED
HumanCITED210370Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
INFERRED
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
Click here to display 17 evidence detail records.
HumanSLC9A16548solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1
Click here to display 17 evidence detail records.
HumanPOU4F35459POU class 4 homeobox 3
INFERRED
HumanPOU4F15457POU class 4 homeobox 1
Click here to display 17 evidence detail records.
HumanPAX25076paired box 2
INFERRED
HumanNTRK34916neurotrophic tyrosine kinase, receptor, type 3
INFERRED
HumanNTRK24915neurotrophic tyrosine kinase, receptor, type 2
Click here to display 17 evidence detail records.
HumanNTF44909neurotrophin 4
INFERRED
HumanNEUROD14760neuronal differentiation 1
Click here to display 17 evidence detail records.
HumanMYO7A4647myosin VIIA
INFERRED
HumanMYO64646myosin VI
INFERRED
HumanMAN2B14125mannosidase, alpha, class 2B, member 1
Click here to display 17 evidence detail records.
HumanKCNJ103766potassium inwardly-rectifying channel, subfamily J, member 10
INFERRED
HumanHOXA13198homeobox A1
INFERRED
HumanGABRB32562gamma-aminobutyric acid (GABA) A receptor, beta 3
INFERRED
HumanEYA12138eyes absent homolog 1 (Drosophila)
INFERRED
HumanATF21386activating transcription factor 2
Click here to display 17 evidence detail records.
HumanBDNF627brain-derived neurotrophic factor
Click here to display 17 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002856abnormal vestibular ganglion morphology0self