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Details
Link-It Detail - Jax Mouse Phenotype - abnormal retinal neuronal layer morphology
Debug Stats
  • ### Total Build Time: 153 ms 23.318 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 412 bytes
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  • CONCEPT_GENES gt=143 ms Completed: 143 ms rowSize= 15.665 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.180 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal retinal neuronal layer morphology MP:0006069
Definition (1)
any structural anomaly of any of the neuronal layers that make up the retina, including the ganglion cell, inner plexiform, inner nuclear, outer plexiform, outer nuclear layers, the inner and outer segments
Parents (1)
img abnormal retinal layer morphology MP:0003727
Children (7)
img abnormal retinal outer plexiform layer morphology MP:0003732
img abnormal retinal ganglion layer morphology MP:0005241
img abnormal retinal inner plexiform layer morphology MP:0003734
img abnormal retinal outer nuclear layer morphology MP:0003731
img abnormal retinal inner nuclear layer morphology MP:0003733
img abnormal retinal photoreceptor layer morphology MP:0003728
img abnormal retinal nerve fiber layer morphology MP:0006303
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053918img abnormal retinal layer morphology MP:0003727
Genes (249)

Species:
human : 249
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SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanPRSS56646960protease, serine, 56
INFERRED
HumanCPLX3594855complexin 3
INFERRED
HumanBARHL2343472BarH-like homeobox 2
INFERRED
HumanRD3343035retinal degeneration 3
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
Click here to display 73 evidence detail records.
HumanCCDC66285331coiled-coil domain containing 66
INFERRED
HumanLAMA1284217laminin, alpha 1
INFERRED
HumanNPHP4261734nephronophthisis 4
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
Click here to display 73 evidence detail records.
HumanATOH7220202atonal homolog 7 (Drosophila)
Click here to display 73 evidence detail records.
HumanLCA5167691Leber congenital amaurosis 5
INFERRED
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED
HumanNXNL2158046nucleoredoxin-like 2
INFERRED
HumanRDH12145226retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
Click here to display 73 evidence detail records.
HumanEGFLAM133584EGF-like, fibronectin type III and laminin G domains
INFERRED
HumanTTC8123016tetratricopeptide repeat domain 8
INFERRED
HumanFOXN4121643forkhead box N4
Click here to display 73 evidence detail records.
HumanFAT3120114FAT atypical cadherin 3
Click here to display 73 evidence detail records.
HumanNXNL1115861nucleoredoxin-like 1
INFERRED
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
INFERRED
HumanRDH13112724retinol dehydrogenase 13 (all-trans/9-cis)
INFERRED
HumanOPN494233opsin 4
INFERRED
HumanRP1L194137retinitis pigmentosa 1-like 1
INFERRED
HumanCACNA2D493589calcium channel, voltage-dependent, alpha 2/delta subunit 4
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006069abnormal retinal neuronal layer morphology0self