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Details
Link-It Detail - Jax Mouse Phenotype - abnormal spinal cord grey matter morphology
Debug Stats
  • ### Total Build Time: 64 ms 21.489 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 414 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 412 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 201 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=0 Completed: 0 ms rowSize= 586 bytes
  • CONCEPT_CHILDREN gt=8 ms Completed: 8 ms rowSize= 1.983 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.577 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=48 ms Completed: 48 ms rowSize= 15.028 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.181 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal spinal cord grey matter morphology MP:0008503
Definition (1)
any structural anomaly of the ridge-shaped grey matter of the spinal cord that extends longitudinally through the center of each half of the spinal cord, and are largely or entirely composed of nerve cell bodies and their dendrites and some supportive tissue
Synonyms (1)
"abnormal spinal cord gray matter morphology" EXACT
Parents (1)
img abnormal spinal cord morphology MP:0000955
Children (4)
img abnormal motor neuron morphology MP:0000937
img abnormal spinal cord interneuron morphology MP:0004100
img abnormal spinal cord ventral horn morphology MP:0005112
img abnormal spinal cord dorsal horn morphology MP:0006282
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal spinal cord morphology MP:0000955
Genes (164)

Species:
human : 164
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDRAXIN374946dorsal inhibitory axon guidance protein
INFERRED
HumanKIF7374654kinesin family member 7
INFERRED
HumanVSX2338917visual system homeobox 2
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanFBXO45200933F-box protein 45
Click here to display 8 evidence detail records.
HumanGDF7151449growth differentiation factor 7
INFERRED
HumanUNC5A90249unc-5 homolog A (C. elegans)
INFERRED
HumanLHX489884LIM homeobox 4
INFERRED
HumanKISS1R84634KISS1 receptor
INFERRED
HumanGDPD581544glycerophosphodiester phosphodiesterase domain containing 5
INFERRED
HumanFUZ80199fuzzy planar cell polarity protein
INFERRED
HumanDYNC2H179659dynein, cytoplasmic 2, heavy chain 1
INFERRED
HumanISL264843ISL LIM homeobox 2
INFERRED
HumanROBO364221roundabout, axon guidance receptor, homolog 3 (Drosophila)
INFERRED
HumanNEUROG263973neurogenin 2
INFERRED
HumanSLC5A760482solute carrier family 5 (sodium/choline cotransporter), member 7
INFERRED
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
INFERRED
HumanISLR257611immunoglobulin superfamily containing leucine-rich repeat 2
INFERRED
HumanSCYL157410SCY1-like 1 (S. cerevisiae)
INFERRED
HumanLHX956956LIM homeobox 9
INFERRED
HumanIFT12255764intraflagellar transport 122 homolog (Chlamydomonas)
INFERRED
HumanHHAT55733hedgehog acyltransferase
INFERRED
HumanWNT454361wingless-type MMTV integration site family, member 4
INFERRED
HumanBCL11A53335B-cell CLL/lymphoma 11A (zinc finger protein)
INFERRED
HumanATP8A251761ATPase, aminophospholipid transporter, class I, type 8A, member 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008503abnormal spinal cord grey matter morphology0self