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Details
Link-It Detail - Jax Mouse Phenotype - abnormal optic cup morphology
Debug Stats
  • ### Total Build Time: 31 ms 13.409 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 417 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 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= 579 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.566 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 9.174 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal optic cup morphology MP:0004269
Definition (1)
any structural anomaly of double walled structured formed by expansion and invagination of the distal end of the optic vesicle that develops into the pigmented and sensory layers of the retina while the mouth of the optic cup eventually forms the pupil of the eye
Parents (1)
img abnormal eye development MP:0001286
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053915img abnormal eye development MP:0001286
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanVSX2338917visual system homeobox 2
Click here to display 22 evidence detail records.
HumanPYGO290780pygopus homolog 2 (Drosophila)
Click here to display 22 evidence detail records.
HumanRAB2351715RAB23, member RAS oncogene family
Click here to display 22 evidence detail records.
HumanCRIM151232cysteine rich transmembrane BMP regulator 1 (chordin-like)
Click here to display 22 evidence detail records.
HumanBRD123774bromodomain containing 1
Click here to display 22 evidence detail records.
HumanALDH1A28854aldehyde dehydrogenase 1 family, member A2
Click here to display 22 evidence detail records.
HumanHESX18820HESX homeobox 1
Click here to display 22 evidence detail records.
HumanARID1A8289AT rich interactive domain 1A (SWI-like)
Click here to display 22 evidence detail records.
HumanSMO6608smoothened, frizzled family receptor
Click here to display 22 evidence detail records.
HumanRPL246152ribosomal protein L24
Click here to display 22 evidence detail records.
HumanPAX65080paired box 6
Click here to display 22 evidence detail records.
HumanPAX25076paired box 2
Click here to display 22 evidence detail records.
HumanMITF4286microphthalmia-associated transcription factor
Click here to display 22 evidence detail records.
HumanGLI32737GLI family zinc finger 3
Click here to display 22 evidence detail records.
HumanPHC11911polyhomeotic homolog 1 (Drosophila)
Click here to display 22 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004269abnormal optic cup morphology0self