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Details
Link-It Detail - Jax Mouse Phenotype - abnormal astrocyte number
Debug Stats
  • ### Total Build Time: 57 ms 19.797 KB
  • CONCEPT_NAME gt=3 ms Completed: 2 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 326 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 183 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=5 ms Completed: 5 ms rowSize= 584 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.021 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.575 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=36 ms Completed: 36 ms rowSize= 14.456 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal astrocyte number MP:0012064
Definition (1)
anomaly in the number of the large neuroglial (macroglial) cells in the central nervous system - the largest and most numerous neuroglial cells in the brain and spinal cord
Synonyms (1)
"abnormal astroglia number" EXACT
Parents (1)
img abnormal astrocyte morphology MP:0002182
Children (2)
img decreased astrocyte number MP:0012066
img increased astrocyte number MP:0012065
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal astrocyte morphology MP:0002182
Genes (76)

Species:
human : 76
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Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanLRRK2120892leucine-rich repeat kinase 2
INFERRED
HumanMPP564398membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5)
INFERRED
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
INFERRED
HumanSCYL157410SCY1-like 1 (S. cerevisiae)
INFERRED
HumanGJC257165gap junction protein, gamma 2, 47kDa
INFERRED
HumanCOQ957017coenzyme Q9 homolog (S. cerevisiae)
INFERRED
HumanVAC1455697Vac14 homolog (S. cerevisiae)
INFERRED
HumanPI4K2A55361phosphatidylinositol 4-kinase type 2 alpha
INFERRED
HumanCLN654982ceroid-lipofuscinosis, neuronal 6, late infantile, variant
INFERRED
HumanPOMT229954protein-O-mannosyltransferase 2
INFERRED
HumanTRIB228951tribbles homolog 2 (Drosophila)
INFERRED
HumanDNAI127019dynein, axonemal, intermediate chain 1
INFERRED
HumanCNTNAP226047contactin associated protein-like 2
INFERRED
HumanLTN126046listerin E3 ubiquitin protein ligase 1
INFERRED
HumanNCSTN23385nicastrin
INFERRED
HumanMGRN123295mahogunin ring finger 1, E3 ubiquitin protein ligase
INFERRED
HumanARSG22901arylsulfatase G
INFERRED
HumanPDCD1011235programmed cell death 10
INFERRED
HumanAFG3L210939AFG3 ATPase family member 3-like 2 (S. cerevisiae)
INFERRED
HumanCERS110715ceramide synthase 1
INFERRED
HumanATG710533autophagy related 7
INFERRED
HumanHAX110456HCLS1 associated protein X-1
INFERRED
HumanNR1H310062nuclear receptor subfamily 1, group H, member 3
INFERRED
HumanFIG49896FIG4 homolog, SAC1 lipid phosphatase domain containing (S. cerevisiae)
INFERRED
HumanEI249538etoposide induced 2.4
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0012064abnormal astrocyte number0self