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Details
Link-It Detail - Jax Mouse Phenotype - abnormal retina morphology
Debug Stats
  • ### Total Build Time: 1,508 ms 30.420 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_GENES gt=1,496 ms Completed: 1.496 Seconds rowSize= 16.032 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal retina morphology MP:0001325
Definition (1)
any structural anomaly of the thin layer of neural tissue lining the back of the eyeball which contains visual receptors
Synonyms (1)
"retina abnormalities" BROAD
Parents (1)
img abnormal ocular fundus morphology MP:0002864
Children (22)
img abnormal retinal vasculature morphology MP:0002792
img retinal degeneration MP:0001326
img abnormal retina inner limiting membrane morphology MP:0010235
img retinal fibrosis MP:0006186
img decreased ventral retina size MP:0010707
img decreased susceptibility to induced retinal damage MP:0003455
img abnormal retinal bipolar cell morphology MP:0006073
img abnormal amacrine cell morphology MP:0005240
img retinal deposits MP:0006187
img abnormal retina outer limiting membrane morphology MP:0010236
img retina hypoplasia MP:0002984
img retinal hemorrhage MP:0006185
img absent retina MP:0009773
img abnormal total retina thickness MP:0011963
img abnormal Muller cell morphology MP:0005547
img retinal detachment MP:0003099
img retinal gliosis MP:0009392
img abnormal retinal development MP:0009772
img retina coloboma MP:0010715
img retina hyperplasia MP:0001329
img abnormal retinal layer morphology MP:0003727
img abnormal horizontal cell morphology MP:0006068
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053916img abnormal ocular fundus morphology MP:0002864
Genes (418)

Species:
human : 418
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
Click here to display 282 evidence detail records.
HumanCRB2286204crumbs homolog 2 (Drosophila)
Click here to display 282 evidence detail records.
HumanCCDC66285331coiled-coil domain containing 66
INFERRED
HumanLAMA1284217laminin, alpha 1
Click here to display 282 evidence detail records.
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
INFERRED
HumanNPHP4261734nephronophthisis 4
Click here to display 282 evidence detail records.
HumanPTF1A256297pancreas specific transcription factor, 1a
Click here to display 282 evidence detail records.
HumanTBC1D32221322TBC1 domain family, member 32
INFERRED
HumanATOH7220202atonal homolog 7 (Drosophila)
Click here to display 282 evidence detail records.
HumanBMPER168667BMP binding endothelial regulator
INFERRED
HumanLCA5167691Leber congenital amaurosis 5
INFERRED
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED
HumanFREM1158326FRAS1 related extracellular matrix 1
Click here to display 282 evidence detail records.
HumanNXNL2158046nucleoredoxin-like 2
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
Click here to display 282 evidence detail records.
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:0001325abnormal retina morphology0self