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Details
Link-It Detail - Jax Mouse Phenotype - abnormal spinal cord ventral horn morphology
Debug Stats
  • ### Total Build Time: 83 ms 13.561 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 416 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 222 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 191 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 598 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 603 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.589 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=50 ms Completed: 50 ms rowSize= 8.663 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.182 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal spinal cord ventral horn morphology MP:0005112
Definition (1)
any structural anomaly of the ventral grey column of the spinal cord
Synonyms (1)
"abnormal anterior horn morphology" EXACT
Parents (1)
img abnormal spinal cord grey matter morphology MP:0008503
Children (1)
img decreased spinal cord ventral horn cell number MP:0005113
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal spinal cord grey matter morphology MP:0008503
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanKIF1B23095kinesin family member 1B
Click here to display 27 evidence detail records.
HumanRIMS122999regulating synaptic membrane exocytosis 1
Click here to display 27 evidence detail records.
HumanOLIG210215oligodendrocyte lineage transcription factor 2
Click here to display 27 evidence detail records.
HumanPLA2G68398phospholipase A2, group VI (cytosolic, calcium-independent)
Click here to display 27 evidence detail records.
HumanVEGFA7422vascular endothelial growth factor A
Click here to display 27 evidence detail records.
HumanTTPA7274tocopherol (alpha) transfer protein
Click here to display 27 evidence detail records.
HumanSNCA6622synuclein, alpha (non A4 component of amyloid precursor)
Click here to display 27 evidence detail records.
HumanPITPNA5306phosphatidylinositol transfer protein, alpha
Click here to display 27 evidence detail records.
HumanGLRB2743glycine receptor, beta
Click here to display 27 evidence detail records.
HumanCLN82055ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
Click here to display 27 evidence detail records.
HumanEEF1A21917eukaryotic translation elongation factor 1 alpha 2
Click here to display 27 evidence detail records.
HumanDYNC1H11778dynein, cytoplasmic 1, heavy chain 1
INFERRED
HumanCDK51020cyclin-dependent kinase 5
Click here to display 27 evidence detail records.
HumanCACNA1S779calcium channel, voltage-dependent, L type, alpha 1S subunit
Click here to display 27 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005112abnormal spinal cord ventral horn morphology0self