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Details
Link-It Detail - Jax Mouse Phenotype - abnormal uvea morphology
Debug Stats
  • ### Total Build Time: 55 ms 20.386 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 376 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 273 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 172 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 578 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.471 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.565 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=52 ms Completed: 52 ms rowSize= 14.677 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal uvea morphology MP:0005197
Definition (1)
any structural anomaly of the pigmented vascular coat of the eyeball, consisting of the iris, ciliary body, and choroid
Synonyms (1)
"uvea dysplasia" EXACT
Parents (1)
img abnormal eye morphology MP:0002092
Children (3)
img uveitis MP:0005515
img abnormal posterior uvea morphology MP:0005196
img abnormal anterior uvea morphology MP:0005194
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053914img abnormal eye morphology MP:0002092
Genes (112)

Species:
human : 112
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanPRSS56646960protease, serine, 56
INFERRED
HumanSH3PXD2B285590SH3 and PX domains 2B
INFERRED
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
INFERRED
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
INFERRED
HumanEGLN3112399egl-9 family hypoxia-inducible factor 3
INFERRED
HumanHPS489781Hermansky-Pudlak syndrome 4
INFERRED
HumanSLX484464SLX4 structure-specific endonuclease subunit
INFERRED
HumanHPS384343Hermansky-Pudlak syndrome 3
INFERRED
HumanDTNBP184062dystrobrevin binding protein 1
INFERRED
HumanHPS679803Hermansky-Pudlak syndrome 6
INFERRED
HumanMLPH79083melanophilin
INFERRED
HumanKXD179036KxDL motif containing 1
INFERRED
HumanVPS33A65082vacuolar protein sorting 33 homolog A (S. cerevisiae)
INFERRED
HumanSMOC164093SPARC related modular calcium binding 1
INFERRED
HumanLGR455366leucine-rich repeat containing G protein-coupled receptor 4
INFERRED
HumanBLOC1S455330biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino
INFERRED
HumanGLCE26035glucuronic acid epimerase
INFERRED
HumanPVRL325945poliovirus receptor-related 3
INFERRED
HumanRAB3823682RAB38, member RAS oncogene family
INFERRED
HumanGRIP123426glutamate receptor interacting protein 1
INFERRED
HumanTDRD723424tudor domain containing 7
INFERRED
HumanHPS511234Hermansky-Pudlak syndrome 5
INFERRED
HumanKERA11081keratocan
INFERRED
HumanPPP1R13L10848protein phosphatase 1, regulatory subunit 13 like
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005197abnormal uvea morphology0self