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Details
Link-It Detail - Jax Mouse Phenotype - abnormal nervous system morphology
Debug Stats
  • ### Total Build Time: 1,048 ms 26.051 KB
  • CONCEPT_NAME gt=13 ms Completed: 13 ms rowSize= 396 bytes
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  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 201 bytes
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  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=1,024 ms Completed: 1.024 Seconds rowSize= 15.515 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal nervous system morphology MP:0003632
Definition (1)
any structural 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 central nervous system morphology" NARROW
Parents (1)
img nervous system phenotype MP:0003631
Children (13)
img abnormal innervation MP:0002184
img abnormal autonomic nervous system morphology MP:0002751
img amyloid beta deposits MP:0003329
img abnormal neuron morphology MP:0002882
img abnormal spinal cord morphology MP:0000955
img alpha-synuclein inclusion body MP:0008493
img abnormal nervous system development MP:0003861
img abnormal glial cell morphology MP:0003634
img abnormal brain morphology MP:0002152
img abnormal somatic nervous system morphology MP:0002752
img abnormal ependyma morphology MP:0002653
img abnormal meninges morphology MP:0005623
img abnormal nervous system tract morphology MP:0000778
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036313img nervous system phenotype MP:0003631
Genes (1987)

Species:
human : 1987
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanOCLN100506658occludin
INFERRED
HumanFOXO6100132074forkhead box O6
INFERRED
HumanISPD729920isoprenoid synthase domain containing
INFERRED
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanSKOR2652991SKI family transcriptional corepressor 2
INFERRED
HumanPRSS56646960protease, serine, 56
INFERRED
HumanCBLN3643866cerebellin 3 precursor
Click here to display 161 evidence detail records.
HumanCPLX3594855complexin 3
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanNRARP441478NOTCH-regulated ankyrin repeat protein
INFERRED
HumanLHX8431707LIM homeobox 8
INFERRED
HumanHELT391723helt bHLH transcription factor
INFERRED
HumanOR8A1390275olfactory receptor, family 8, subfamily A, member 1
INFERRED
HumanFEZF1389549FEZ family zinc finger 1
INFERRED
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanFAM212A389119family with sequence similarity 212, member A
INFERRED
HumanHES5388585hairy and enhancer of split 5 (Drosophila)
INFERRED
HumanSHISA2387914shisa family member 2
INFERRED
HumanINSC387755inscuteable homolog (Drosophila)
INFERRED
HumanNHLRC1378884NHL repeat containing 1
INFERRED
HumanAGRN375790agrin
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanDRAXIN374946dorsal inhibitory axon guidance protein
INFERRED
HumanKIF7374654kinesin family member 7
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003632abnormal nervous system morphology0self