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Details
Link-It Detail - Jax Mouse Phenotype - neuron degeneration
Debug Stats
  • ### Total Build Time: 207 ms 24.825 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 366 bytes
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  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 3.769 KB
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  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=201 ms Completed: 201 ms rowSize= 15.194 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.157 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
neuron degeneration MP:0003224
Definition (1)
a retrogressive impairment of function or destruction of the functional cells of the nervous system that receive, conduct, and transmit impulses
Parents (2)
img abnormal neuron morphology MP:0002882
img neurodegeneration MP:0002229
Children (8)
img Purkinje cell degeneration MP:0000876
img motor neuron degeneration MP:0000938
img hippocampal neuron degeneration MP:0000811
img amacrine cell degeneration MP:0008103
img retinal ganglion cell degeneration MP:0008067
img cochlear hair cell degeneration MP:0004362
img retinal photoreceptor degeneration MP:0008450
img vestibular hair cell degeneration MP:0004324
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal neuron morphology MP:0002882
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img neurodegeneration MP:0002229
Genes (266)

Species:
human : 266
Page Size
Current 25
  Page 1 of 11
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanPRSS56646960protease, serine, 56
INFERRED
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanRD3343035retinal degeneration 3
INFERRED
HumanCCDC66285331coiled-coil domain containing 66
INFERRED
HumanNPAS4266743neuronal PAS domain protein 4
Click here to display 113 evidence detail records.
HumanNPHP4261734nephronophthisis 4
INFERRED
HumanTMIE259236transmembrane inner ear
INFERRED
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanSYNE4163183spectrin repeat containing, nuclear envelope family member 4
INFERRED
HumanEDARADD128178EDAR-associated death domain
INFERRED
HumanLOXHD1125336lipoxygenase homology domains 1
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
INFERRED
HumanRP1L194137retinitis pigmentosa 1-like 1
INFERRED
HumanGJA1084694gap junction protein, alpha 10, 62kDa
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanESPN83715espin
INFERRED
HumanMFRP83552membrane frizzled-related protein
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003224neuron degeneration0self