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Details
Link-It Detail - Jax Mouse Phenotype - abnormal retinal layer morphology
Debug Stats
  • ### Total Build Time: 45 ms 20.693 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 221 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
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  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.511 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.568 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=38 ms Completed: 38 ms rowSize= 15.131 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal retinal layer morphology MP:0003727
Definition (1)
any structural anomaly of any of the layers that make up the retina
Parents (1)
img abnormal retina morphology MP:0001325
Children (3)
img abnormal retinal neuronal layer morphology MP:0006069
img disorganized retinal layers MP:0001328
img abnormal retinal pigment epithelium morphology MP:0005201
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053917img abnormal retina morphology MP:0001325
Genes (292)

Species:
human : 292
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Current 25
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Current 1
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
HumanVSX2338917visual system homeobox 2
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
Click here to display 30 evidence detail records.
HumanCCDC66285331coiled-coil domain containing 66
INFERRED
HumanLAMA1284217laminin, alpha 1
INFERRED
HumanSLC24A5283652solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
INFERRED
HumanNPHP4261734nephronophthisis 4
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanTBC1D32221322TBC1 domain family, member 32
INFERRED
HumanATOH7220202atonal homolog 7 (Drosophila)
INFERRED
HumanLCA5167691Leber congenital amaurosis 5
INFERRED
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED
HumanNXNL2158046nucleoredoxin-like 2
INFERRED
HumanRDH12145226retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
INFERRED
HumanEGFLAM133584EGF-like, fibronectin type III and laminin G domains
INFERRED
HumanTTC8123016tetratricopeptide repeat domain 8
INFERRED
HumanFOXN4121643forkhead box N4
INFERRED
HumanFAT3120114FAT atypical cadherin 3
INFERRED
HumanNXNL1115861nucleoredoxin-like 1
INFERRED
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
INFERRED
HumanRDH13112724retinol dehydrogenase 13 (all-trans/9-cis)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003727abnormal retinal layer morphology0self