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Details
Link-It Detail - Jax Mouse Phenotype - abnormal ocular fundus morphology
Debug Stats
  • ### Total Build Time: 112 ms 21.152 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 394 bytes
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  • CONCEPT_GENES gt=82 ms Completed: 82 ms rowSize= 15.271 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.171 KB
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Jax Mouse Phenotype (1)
abnormal ocular fundus morphology MP:0002864
Definition (1)
any structural anomaly of the posterior concave interior of the eye, consisting of the retina, the choroid, the posterior segment of the sclera, the optic disk, and blood vessels, visible by an ophthalmoscope
Synonyms (1)
"abnormal fundus oculus" EXACT
Parents (1)
img abnormal posterior eye segment morphology MP:0005195
Children (3)
img abnormal retina morphology MP:0001325
img abnormal optic disc morphology MP:0008259
img abnormal posterior uvea morphology MP:0005196
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053915img abnormal posterior eye segment morphology MP:0005195
Genes (430)

Species:
human : 430
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanPRSS56646960protease, serine, 56
INFERRED
HumanCPLX3594855complexin 3
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanNRARP441478NOTCH-regulated ankyrin repeat protein
INFERRED
HumanHES5388585hairy and enhancer of split 5 (Drosophila)
INFERRED
HumanBARHL2343472BarH-like homeobox 2
INFERRED
HumanRD3343035retinal degeneration 3
INFERRED
HumanVSX2338917visual system homeobox 2
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
INFERRED
HumanCCDC66285331coiled-coil domain containing 66
INFERRED
HumanLAMA1284217laminin, alpha 1
Click here to display 38 evidence detail records.
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
Click here to display 38 evidence detail records.
HumanNPHP4261734nephronophthisis 4
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanTBC1D32221322TBC1 domain family, member 32
INFERRED
HumanATOH7220202atonal homolog 7 (Drosophila)
INFERRED
HumanBMPER168667BMP binding endothelial regulator
INFERRED
HumanLCA5167691Leber congenital amaurosis 5
INFERRED
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED
HumanFREM1158326FRAS1 related extracellular matrix 1
INFERRED
HumanNXNL2158046nucleoredoxin-like 2
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanTICAM1148022toll-like receptor adaptor molecule 1
INFERRED
HumanRDH12145226retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002864abnormal ocular fundus morphology0self