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Details
Link-It Detail - Jax Mouse Phenotype - thin retinal outer nuclear layer
Debug Stats
  • ### Total Build Time: 397 ms 21.714 KB
  • CONCEPT_NAME gt=14 ms Completed: 14 ms rowSize= 392 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 251 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 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=3 ms Completed: 3 ms rowSize= 601 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.589 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=372 ms Completed: 372 ms rowSize= 17.588 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.170 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
thin retinal outer nuclear layer MP:0008515
Definition (1)
reduced thickness of the retinal layer that contains the nuclei and cell bodies of rods and cones
Parents (1)
img abnormal retinal outer nuclear layer thickness MP:0011997
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:000539111img abnormal retinal outer nuclear layer thickness MP:0011997
Genes (73)

Species:
human : 73
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SpeciesGeneGeneIdGene NameEvidence
HumanRD3343035retinal degeneration 3
Click here to display 145 evidence detail records.
HumanCRB2286204crumbs homolog 2 (Drosophila)
Click here to display 145 evidence detail records.
HumanCCDC66285331coiled-coil domain containing 66
Click here to display 145 evidence detail records.
HumanNPHP4261734nephronophthisis 4
Click here to display 145 evidence detail records.
HumanATOH7220202atonal homolog 7 (Drosophila)
Click here to display 145 evidence detail records.
HumanBBS12166379Bardet-Biedl syndrome 12
Click here to display 145 evidence detail records.
HumanNXNL1115861nucleoredoxin-like 1
Click here to display 145 evidence detail records.
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
Click here to display 145 evidence detail records.
HumanRDH13112724retinol dehydrogenase 13 (all-trans/9-cis)
Click here to display 145 evidence detail records.
HumanRP1L194137retinitis pigmentosa 1-like 1
Click here to display 145 evidence detail records.
HumanMFRP83552membrane frizzled-related protein
Click here to display 145 evidence detail records.
HumanDNAJC580331DnaJ (Hsp40) homolog, subfamily C, member 5
Click here to display 145 evidence detail records.
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
Click here to display 145 evidence detail records.
HumanCEP29080184centrosomal protein 290kDa
Click here to display 145 evidence detail records.
HumanFKRP79147fukutin related protein
Click here to display 145 evidence detail records.
HumanMPP564398membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5)
Click here to display 145 evidence detail records.
HumanSEMA4A64218sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
Click here to display 145 evidence detail records.
HumanRPGRIP157096retinitis pigmentosa GTPase regulator interacting protein 1
Click here to display 145 evidence detail records.
HumanCABP457010calcium binding protein 4
Click here to display 145 evidence detail records.
HumanMDM156890Mdm1 nuclear protein homolog (mouse)
Click here to display 145 evidence detail records.
HumanPOMGNT155624protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
Click here to display 145 evidence detail records.
HumanLGR455366leucine-rich repeat containing G protein-coupled receptor 4
Click here to display 145 evidence detail records.
HumanAHI154806Abelson helper integration site 1
Click here to display 145 evidence detail records.
HumanDFNB3125861deafness, autosomal recessive 31
Click here to display 145 evidence detail records.
HumanFSCN225794fascin homolog 2, actin-bundling protein, retinal (Strongylocentrotus purpuratus)
Click here to display 145 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008515thin retinal outer nuclear layer0self