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Details
Link-It Detail - Jax Mouse Phenotype - decreased sensory neuron number
Debug Stats
  • ### Total Build Time: 63 ms 25.063 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 301 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 187 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
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  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.432 KB
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  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=56 ms Completed: 56 ms rowSize= 15.175 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
decreased sensory neuron number MP:0000966
Definition (1)
fewer than normal numbers of cells that innervate an effector (muscle or glandular) tissue and are responsible for transmission of sensory impulses
Synonyms (1)
"reduced sensory neuron number" EXACT
Parents (2)
img decreased neuron number MP:0008948
img abnormal sensory neuron morphology MP:0000965
Children (5)
img decreased retinal ganglion cell number MP:0006309
img decreased amacrine cell number MP:0008106
img decreased cochlear hair cell number MP:0004408
img decreased retinal photoreceptor cell number MP:0001327
img decreased vestibular hair cell number MP:0004328
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img decreased neuron number MP:0008948
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal sensory neuron morphology MP:0000965
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal sensory neuron morphology MP:0000965
Genes (139)

Species:
human : 139
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanBARHL2343472BarH-like homeobox 2
INFERRED
HumanRD3343035retinal degeneration 3
INFERRED
HumanHMX3340784H6 family homeobox 3
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
Click here to display 49 evidence detail records.
HumanATOH7220202atonal homolog 7 (Drosophila)
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanNXNL2158046nucleoredoxin-like 2
INFERRED
HumanFOXN4121643forkhead box N4
INFERRED
HumanNXNL1115861nucleoredoxin-like 1
INFERRED
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
INFERRED
HumanRP1L194137retinitis pigmentosa 1-like 1
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanSTRA664220stimulated by retinoic acid 6
INFERRED
HumanSEMA4A64218sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
INFERRED
HumanSMOC164093SPARC related modular calcium binding 1
INFERRED
HumanCDH2364072cadherin-related 23
INFERRED
HumanNEUROG263973neurogenin 2
INFERRED
HumanNEUROD458158neuronal differentiation 4
INFERRED
HumanSEMA6A57556sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A
Click here to display 49 evidence detail records.
HumanHR55806hair growth associated
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000966decreased sensory neuron number0self