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Details
Link-It Detail - Jax Mouse Phenotype - retinal degeneration
Debug Stats
  • ### Total Build Time: 698 ms 21.900 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 368 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 1.568 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=691 ms Completed: 691 ms rowSize= 17.744 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.158 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
retinal degeneration MP:0001326
Definition (1)
retrogressive pathological change in the thin layer of neural tissue lining the back of the eyeball, which contains visual receptors and can result in the impairment or cessation of retinal neural function
Parents (1)
img abnormal retina morphology MP:0001325
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053917img abnormal retina morphology MP:0001325
Genes (80)

Species:
human : 80
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SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
Click here to display 210 evidence detail records.
HumanRD3343035retinal degeneration 3
Click here to display 210 evidence detail records.
HumanCRB2286204crumbs homolog 2 (Drosophila)
Click here to display 210 evidence detail records.
HumanBBS12166379Bardet-Biedl syndrome 12
Click here to display 210 evidence detail records.
HumanTTC8123016tetratricopeptide repeat domain 8
Click here to display 210 evidence detail records.
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
Click here to display 210 evidence detail records.
HumanCDHR192211cadherin-related family member 1
Click here to display 210 evidence detail records.
HumanMFRP83552membrane frizzled-related protein
Click here to display 210 evidence detail records.
HumanCEP29080184centrosomal protein 290kDa
Click here to display 210 evidence detail records.
HumanPANK280025pantothenate kinase 2
Click here to display 210 evidence detail records.
HumanLPCAT179888lysophosphatidylcholine acyltransferase 1
Click here to display 210 evidence detail records.
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
Click here to display 210 evidence detail records.
HumanMPP564398membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5)
Click here to display 210 evidence detail records.
HumanSEMA4A64218sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
Click here to display 210 evidence detail records.
HumanSMOC164093SPARC related modular calcium binding 1
Click here to display 210 evidence detail records.
HumanMCOLN157192mucolipin 1
Click here to display 210 evidence detail records.
HumanMDM156890Mdm1 nuclear protein homolog (mouse)
Click here to display 210 evidence detail records.
HumanCLN654982ceroid-lipofuscinosis, neuronal 6, late infantile, variant
Click here to display 210 evidence detail records.
HumanPRPF3126121pre-mRNA processing factor 31
Click here to display 210 evidence detail records.
HumanDFNB3125861deafness, autosomal recessive 31
Click here to display 210 evidence detail records.
HumanFSCN225794fascin homolog 2, actin-bundling protein, retinal (Strongylocentrotus purpuratus)
Click here to display 210 evidence detail records.
HumanAIPL123746aryl hydrocarbon receptor interacting protein-like 1
Click here to display 210 evidence detail records.
HumanCRB123418crumbs homolog 1 (Drosophila)
Click here to display 210 evidence detail records.
HumanAGTPBP123287ATP/GTP binding protein 1
Click here to display 210 evidence detail records.
HumanPRPF810594pre-mRNA processing factor 8
Click here to display 210 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001326retinal degeneration0self