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Details
Link-It Detail - Jax Mouse Phenotype - abnormal horizontal cell morphology
Debug Stats
  • ### Total Build Time: 29 ms 16.175 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 398 bytes
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  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 8.277 KB
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Jax Mouse Phenotype (1)
abnormal horizontal cell morphology MP:0006068
Definition (1)
any structural anomaly of the laterally interconnecting neurons in the outer plexiform layer of the retina that connect rods of one part of the retina with cones in another part of the retina
Parents (2)
img abnormal retina morphology MP:0001325
img abnormal sensory neuron morphology MP:0000965
Children (1)
img absent horizontal cells MP:0008107
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053917img abnormal retina morphology MP:0001325
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036316img abnormal sensory neuron morphology MP:0000965
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal sensory neuron morphology MP:0000965
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanFOXN4121643forkhead box N4
INFERRED
HumanGJA1084694gap junction protein, alpha 10, 62kDa
Click here to display 22 evidence detail records.
HumanMEGF1084466multiple EGF-like-domains 10
Click here to display 22 evidence detail records.
HumanMEGF1184465multiple EGF-like-domains 11
Click here to display 22 evidence detail records.
HumanNEUROD458158neuronal differentiation 4
Click here to display 22 evidence detail records.
HumanERC226059ELKS/RAB6-interacting/CAST family member 2
Click here to display 22 evidence detail records.
HumanRBL25934retinoblastoma-like 2 (p130)
Click here to display 22 evidence detail records.
HumanPROX15629prospero homeobox 1
INFERRED
HumanCRX1406cone-rod homeobox
Click here to display 22 evidence detail records.
HumanCNGA31261cyclic nucleotide gated channel alpha 3
Click here to display 22 evidence detail records.
HumanCNGB11258cyclic nucleotide gated channel beta 1
Click here to display 22 evidence detail records.
HumanCACNA1F778calcium channel, voltage-dependent, L type, alpha 1F subunit
Click here to display 22 evidence detail records.
HumanATRX546alpha thalassemia/mental retardation syndrome X-linked
Click here to display 22 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006068abnormal horizontal cell morphology0self