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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vestibulocochlear ganglion morphology
Debug Stats
  • ### Total Build Time: 82 ms 16.094 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 420 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 346 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 203 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
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  • CONCEPT_PARENTS gt=8 ms Completed: 8 ms rowSize= 1.037 KB
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 590 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.928 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=51 ms Completed: 51 ms rowSize= 9.278 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.184 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal vestibulocochlear ganglion morphology MP:0003703
Definition (1)
any structural anomaly of the group of neuron cell bodies associated with the eighth cranial nerve during embryogenesis; splits in later development to form the cochlear and vestibular ganglia
Synonyms (1)
"abnormal vestibulocochlear ganglia morphology" EXACT
Parents (2)
img abnormal cranial ganglia morphology MP:0001081
img abnormal nervous system development MP:0003861
Children (1)
img absent vestibulocochlear ganglion MP:0004313
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal cranial ganglia morphology MP:0001081
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal nervous system development MP:0003861
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 25 evidence detail records.
HumanALDH1A28854aldehyde dehydrogenase 1 family, member A2
Click here to display 25 evidence detail records.
HumanCHRD8646chordin
Click here to display 25 evidence detail records.
HumanTBX16899T-box 1
Click here to display 25 evidence detail records.
HumanSIX16495SIX homeobox 1
INFERRED
HumanSHH6469sonic hedgehog
INFERRED
HumanPAX25076paired box 2
Click here to display 25 evidence detail records.
HumanNTF34908neurotrophin 3
Click here to display 25 evidence detail records.
HumanNEUROD14760neuronal differentiation 1
Click here to display 25 evidence detail records.
HumanHOXA13198homeobox A1
Click here to display 25 evidence detail records.
HumanFOXG12290forkhead box G1
Click here to display 25 evidence detail records.
HumanFGFR22263fibroblast growth factor receptor 2
Click here to display 25 evidence detail records.
HumanFGF102255fibroblast growth factor 10
INFERRED
HumanFGF32248fibroblast growth factor 3
Click here to display 25 evidence detail records.
HumanERBB42066v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 4
Click here to display 25 evidence detail records.
HumanBDNF627brain-derived neurotrophic factor
Click here to display 25 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003703abnormal vestibulocochlear ganglion morphology0self