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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cerebellar molecular layer
Debug Stats
  • ### Total Build Time: 202 ms 20.461 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 398 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 377 bytes
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  • CONCEPT_CHILDREN gt=9 ms Completed: 9 ms rowSize= 588 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.583 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=146 ms Completed: 146 ms rowSize= 15.475 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.173 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cerebellar molecular layer MP:0000889
Definition (1)
any structural anomaly of the outermost layer of the cerebral cortex that contains the parallel fibers of the granule cells, interneurons such as stellate and basket cells, and the dendrites of the underlying Purkinje cells
Synonyms (1)
"abnormal molecular layer" EXACT
Parents (1)
img abnormal cerebellar layer morphology MP:0009956
Children (1)
img thin cerebellar molecular layer MP:0000890
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal cerebellar layer morphology MP:0009956
Genes (47)

Species:
human : 47
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
INFERRED
HumanSKOR2652991SKI family transcriptional corepressor 2
INFERRED
HumanFOXP293986forkhead box P2
INFERRED
HumanNEUROD458158neuronal differentiation 4
INFERRED
HumanKLHL157626kelch-like family member 1
INFERRED
HumanCEND151286cell cycle exit and neuronal differentiation 1
INFERRED
HumanRBFOX223543RNA binding protein, fox-1 homolog (C. elegans) 2
INFERRED
HumanMAPK8IP223542mitogen-activated protein kinase 8 interacting protein 2
INFERRED
HumanIL1RAPL111141interleukin 1 receptor accessory protein-like 1
Click here to display 48 evidence detail records.
HumanNR1D19572nuclear receptor subfamily 1, group D, member 1
Click here to display 48 evidence detail records.
HumanEI249538etoposide induced 2.4
INFERRED
HumanCDK5R18851cyclin-dependent kinase 5, regulatory subunit 1 (p35)
Click here to display 48 evidence detail records.
HumanNUMB8650numb homolog (Drosophila)
INFERRED
HumanUNC5C8633unc-5 homolog C (C. elegans)
Click here to display 48 evidence detail records.
HumanCNTNAP18506contactin associated protein 1
Click here to display 48 evidence detail records.
HumanTHRB7068thyroid hormone receptor, beta
INFERRED
HumanSPTBN26712spectrin, beta, non-erythrocytic 2
Click here to display 48 evidence detail records.
HumanSLC9A16548solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1
Click here to display 48 evidence detail records.
HumanRORA6095RAR-related orphan receptor A
Click here to display 48 evidence detail records.
HumanRNF26045ring finger protein 2
Click here to display 48 evidence detail records.
HumanRBL15933retinoblastoma-like 1 (p107)
INFERRED
HumanPURA5813purine-rich element binding protein A
Click here to display 48 evidence detail records.
HumanPTEN5728phosphatase and tensin homolog
Click here to display 48 evidence detail records.
HumanPRNP5621prion protein
INFERRED
HumanPLXNA25362plexin A2
Click here to display 48 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000889abnormal cerebellar molecular layer0self