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Details
Link-It Detail - Jax Mouse Phenotype - abnormal retinal nerve fiber layer morphology
Debug Stats
  • ### Total Build Time: 14 ms 12.398 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 418 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 256 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 193 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
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  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 8.050 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.183 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal retinal nerve fiber layer morphology MP:0006303
Definition (1)
any structural anomaly of the layer of the retina formed by expansion of the fibers of the optic nerve
Synonyms (1)
"abnormal stratum opticum morphology" EXACT
Parents (1)
img abnormal retinal neuronal layer morphology MP:0006069
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053919img abnormal retinal neuronal layer morphology MP:0006069
Genes (13)

Species:
human : 13
SpeciesGeneGeneIdGene NameEvidence
HumanATOH7220202atonal homolog 7 (Drosophila)
Click here to display 19 evidence detail records.
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
Click here to display 19 evidence detail records.
HumanTSPAN1223554tetraspanin 12
Click here to display 19 evidence detail records.
HumanNR2E17101nuclear receptor subfamily 2, group E, member 1
Click here to display 19 evidence detail records.
HumanSOD16647superoxide dismutase 1, soluble
Click here to display 19 evidence detail records.
HumanPOU4F35459POU class 4 homeobox 3
Click here to display 19 evidence detail records.
HumanPOU4F25458POU class 4 homeobox 2
Click here to display 19 evidence detail records.
HumanPAX25076paired box 2
Click here to display 19 evidence detail records.
HumanOPA14976optic atrophy 1 (autosomal dominant)
Click here to display 19 evidence detail records.
HumanITGA33675integrin, alpha 3 (antigen CD49C, alpha 3 subunit of VLA-3 receptor)
Click here to display 19 evidence detail records.
HumanITGA63655integrin, alpha 6
Click here to display 19 evidence detail records.
HumanASPA443aspartoacylase
Click here to display 19 evidence detail records.
HumanFASLG356Fas ligand (TNF superfamily, member 6)
Click here to display 19 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006303abnormal retinal nerve fiber layer morphology0self