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Details
Link-It Detail - Jax Mouse Phenotype - decreased retinal photoreceptor cell number
Debug Stats
  • ### Total Build Time: 74 ms 27.414 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 414 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 205 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 199 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 1.039 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.036 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 6.977 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=67 ms Completed: 67 ms rowSize= 16.238 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.181 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
decreased retinal photoreceptor cell number MP:0001327
Definition (1)
fewer than the expected number of rods and/or cones
Synonyms (1)
"reduced retinal photoreceptor cell number" EXACT
Parents (2)
img decreased sensory neuron number MP:0000966
img abnormal retinal photoreceptor morphology MP:0001004
Children (2)
img decreased retinal rod cell number MP:0008453
img decreased retinal cone cell number MP:0008446
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img decreased sensory neuron number MP:0000966
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img decreased sensory neuron number MP:0000966
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal retinal photoreceptor morphology MP:0001004
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal retinal photoreceptor morphology MP:0001004
img mammalian phenotype MP:0000001img vision/eye phenotype MP:000539111img abnormal retinal photoreceptor morphology MP:0001004
Genes (51)

Species:
human : 51
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanRD3343035retinal degeneration 3
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
Click here to display 52 evidence detail records.
HumanATOH7220202atonal homolog 7 (Drosophila)
INFERRED
HumanNXNL2158046nucleoredoxin-like 2
INFERRED
HumanNXNL1115861nucleoredoxin-like 1
INFERRED
HumanC1QTNF5114902C1q and tumor necrosis factor related protein 5
INFERRED
HumanRP1L194137retinitis pigmentosa 1-like 1
Click here to display 52 evidence detail records.
HumanSTRA664220stimulated by retinoic acid 6
INFERRED
HumanSEMA4A64218sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
Click here to display 52 evidence detail records.
HumanNEUROG263973neurogenin 2
Click here to display 52 evidence detail records.
HumanNEUROD458158neuronal differentiation 4
Click here to display 52 evidence detail records.
HumanCNGB354714cyclic nucleotide gated channel beta 3
INFERRED
HumanAIPL123746aryl hydrocarbon receptor interacting protein-like 1
Click here to display 52 evidence detail records.
HumanCRB123418crumbs homolog 1 (Drosophila)
Click here to display 52 evidence detail records.
HumanMERTK10461c-mer proto-oncogene tyrosine kinase
Click here to display 52 evidence detail records.
HumanGDF1110220growth differentiation factor 11
Click here to display 52 evidence detail records.
HumanSLC4A79497solute carrier family 4, sodium bicarbonate cotransporter, member 7
Click here to display 52 evidence detail records.
HumanLRAT9227lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
Click here to display 52 evidence detail records.
HumanTYR7299tyrosinase
Click here to display 52 evidence detail records.
HumanTULP17287tubby like protein 1
Click here to display 52 evidence detail records.
HumanTUB7275tubby bipartite transcription factor
Click here to display 52 evidence detail records.
HumanATXN76314ataxin 7
Click here to display 52 evidence detail records.
HumanRS16247retinoschisin 1
INFERRED
HumanRPGR6103retinitis pigmentosa GTPase regulator
INFERRED
HumanRP16101retinitis pigmentosa 1 (autosomal dominant)
Click here to display 52 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001327decreased retinal photoreceptor cell number0self