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Details
Link-It Detail - Jax Mouse Phenotype - abnormal retinal outer nuclear layer thickness
Debug Stats
  • ### Total Build Time: 16 ms 19.629 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 420 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.034 KB
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  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 14.427 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.184 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal retinal outer nuclear layer thickness MP:0011997
Definition (1)
anomaly in the thickness of the retinal layer that contains the nuclei and cell bodies of rods and cones
Parents (1)
img abnormal retinal outer nuclear layer morphology MP:0003731
Children (2)
img thin retinal outer nuclear layer MP:0008515
img thick retinal outer nuclear layer MP:0008517
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:000539110img abnormal retinal outer nuclear layer morphology MP:0003731
Genes (74)

Species:
human : 74
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanRD3343035retinal degeneration 3
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
INFERRED
HumanCCDC66285331coiled-coil domain containing 66
INFERRED
HumanNPHP4261734nephronophthisis 4
INFERRED
HumanATOH7220202atonal homolog 7 (Drosophila)
INFERRED
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED
HumanNXNL1115861nucleoredoxin-like 1
INFERRED
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
INFERRED
HumanRDH13112724retinol dehydrogenase 13 (all-trans/9-cis)
INFERRED
HumanRP1L194137retinitis pigmentosa 1-like 1
INFERRED
HumanMFRP83552membrane frizzled-related protein
INFERRED
HumanDNAJC580331DnaJ (Hsp40) homolog, subfamily C, member 5
INFERRED
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
INFERRED
HumanCEP29080184centrosomal protein 290kDa
INFERRED
HumanFKRP79147fukutin related protein
INFERRED
HumanMPP564398membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5)
INFERRED
HumanSEMA4A64218sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
INFERRED
HumanRPGRIP157096retinitis pigmentosa GTPase regulator interacting protein 1
INFERRED
HumanCABP457010calcium binding protein 4
INFERRED
HumanMDM156890Mdm1 nuclear protein homolog (mouse)
INFERRED
HumanPOMGNT155624protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
INFERRED
HumanLGR455366leucine-rich repeat containing G protein-coupled receptor 4
INFERRED
HumanAHI154806Abelson helper integration site 1
INFERRED
HumanDFNB3125861deafness, autosomal recessive 31
INFERRED
HumanFSCN225794fascin homolog 2, actin-bundling protein, retinal (Strongylocentrotus purpuratus)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011997abnormal retinal outer nuclear layer thickness0self