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Details
Link-It Detail - Jax Mouse Phenotype - abnormal retinal outer nuclear layer morphology
Debug Stats
  • ### Total Build Time: 69 ms 21.641 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 422 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 197 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 597 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 1.521 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=8 ms Completed: 8 ms rowSize= 1.584 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=53 ms Completed: 53 ms rowSize= 15.769 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.185 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal retinal outer nuclear layer morphology MP:0003731
Definition (1)
any structural anomaly of the retinal layer that contains the nuclei and cell bodies of rods and cones
Synonyms (1)
"abnormal outer nuclear layer morphology" EXACT
Parents (1)
img abnormal retinal neuronal layer morphology MP:0006069
Children (3)
img abnormal retinal outer nuclear layer thickness MP:0011997
img retinal outer nuclear layer degeneration MP:0008518
img disorganized retinal outer nuclear layer MP:0008516
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053919img abnormal retinal neuronal layer morphology MP:0006069
Genes (105)

Species:
human : 105
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SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanRD3343035retinal degeneration 3
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
INFERRED
HumanCCDC66285331coiled-coil domain containing 66
INFERRED
HumanNPHP4261734nephronophthisis 4
Click here to display 45 evidence detail records.
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
HumanCACNA2D493589calcium channel, voltage-dependent, alpha 2/delta subunit 4
Click here to display 45 evidence detail records.
HumanARL684100ADP-ribosylation factor-like 6
Click here to display 45 evidence detail records.
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
HumanPANK280025pantothenate kinase 2
Click here to display 45 evidence detail records.
HumanFKRP79147fukutin related protein
INFERRED
HumanMPP564398membrane protein, palmitoylated 5 (MAGUK p55 subfamily member 5)
Click here to display 45 evidence detail records.
HumanSEMA4A64218sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
INFERRED
HumanNEUROD458158neuronal differentiation 4
Click here to display 45 evidence detail records.
HumanMCOLN157192mucolipin 1
Click here to display 45 evidence detail records.
HumanRPGRIP157096retinitis pigmentosa GTPase regulator interacting protein 1
INFERRED
HumanCABP457010calcium binding protein 4
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003731abnormal retinal outer nuclear layer morphology0self