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Details
Link-It Detail - Jax Mouse Phenotype - abnormal nervous system physiology
Debug Stats
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Jax Mouse Phenotype (1)
abnormal nervous system physiology MP:0003633
Definition (1)
any functional anomaly of the extensive, intricate network of electochemical structures in the body that is comprised of the brain, spinal cord, nerves, ganglia and parts of the receptor organs that receive and interpret stimuli and transmit impulses to effector organs to control body functions
Synonyms (1)
"abnormal brain function" NARROW
Parents (1)
img nervous system phenotype MP:0003631
Children (31)
img peripheral nervous system degeneration MP:0000958
img abnormal ependyma motile cilium physiology MP:0011068
img abnormal nervous system electrophysiology MP:0002272
img abnormal somatic nervous system physiology MP:0005423
img abnormal cerebrospinal fluid production MP:0001911
img abnormal pineal gland physiology MP:0011728
img abnormal autonomic nervous system physiology MP:0006276
img seizures MP:0002064
img neurodegeneration MP:0002229
img altered response to CNS ischemic injury MP:0003075
img abnormal glial cell physiology MP:0003690
img abnormal synaptic plasticity MP:0004859
img endoneurial edema MP:0011397
img abnormal nervous system regeneration MP:0004858
img abnormal synaptic transmission MP:0003635
img abnormal endoneurial fluid pressure MP:0011398
img abnormal hippocampus physiology MP:0012006
img abnormal sensorimotor gating MP:0002634
img intracranial hemorrhage MP:0001915
img abnormal neuron physiology MP:0004811
img abnormal hypothalamus physiology MP:0005645
img CNS inflammation MP:0006082
img abnormal pituitary gland physiology MP:0005646
img abnormal central pattern generator function MP:0003880
img abnormal blood-cerebrospinal fluid barrier function MP:0006088
img abnormal myelination MP:0000920
img abnormal dopamine level MP:0001905
img abnormal blood-brain barrier function MP:0005167
img spinal hemorrhage MP:0006054
img abnormal somatosensory cortex physiology MP:0001908
img CNS ischemia MP:0006080
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036313img nervous system phenotype MP:0003631
Genes (1490)

Species:
human : 1490
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanCASP12100506742caspase 12 (gene/pseudogene)
INFERRED
HumanFOXO6100132074forkhead box O6
INFERRED
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanNCF1653361neutrophil cytosolic factor 1
INFERRED
HumanSKOR2652991SKI family transcriptional corepressor 2
INFERRED
HumanPRSS56646960protease, serine, 56
INFERRED
HumanPIRT644139phosphoinositide-interacting regulator of transient receptor potential channels
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanUNC13C440279unc-13 homolog C (C. elegans)
INFERRED
HumanEIF2AK4440275eukaryotic translation initiation factor 2 alpha kinase 4
INFERRED
HumanCCL3L3414062chemokine (C-C motif) ligand 3-like 3
INFERRED
HumanGRID2IP392862glutamate receptor, ionotropic, delta 2 (Grid2) interacting protein
INFERRED
HumanHELT391723helt bHLH transcription factor
INFERRED
HumanFEZF1389549FEZ family zinc finger 1
INFERRED
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanINSC387755inscuteable homolog (Drosophila)
INFERRED
HumanNHLRC1378884NHL repeat containing 1
INFERRED
HumanAGRN375790agrin
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanGJC3349149gap junction protein, gamma 3, 30.2kDa
INFERRED
HumanHCN1348980hyperpolarization activated cyclic nucleotide-gated potassium channel 1
INFERRED
HumanGNAT3346562guanine nucleotide binding protein, alpha transducing 3
INFERRED
HumanRD3343035retinal degeneration 3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003633abnormal nervous system physiology0self