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Details
Link-It Detail - Jax Mouse Phenotype - abnormal amacrine cell number
Debug Stats
  • ### Total Build Time: 15 ms 16.867 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 446 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 189 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.029 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.266 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 8.689 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal amacrine cell number MP:0008104
Definition (1)
anomaly in the number of one of the three types of interneurons found in the inner nuclear layer of the mature retina; they integrate, modulate, and interpose a temporal domain in the visual message presented to the retinal ganglion cells, with which they synapse in the inner plexiform layer
Synonyms (1)
"abnormal amacrine neuron number" EXACT
Parents (1)
img abnormal amacrine cell morphology MP:0005240
Children (2)
img decreased amacrine cell number MP:0008106
img increased amacrine cell number MP:0008105
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img vision/eye phenotype MP:00053918img abnormal amacrine cell morphology MP:0005240
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img abnormal amacrine cell morphology MP:0005240
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal amacrine cell morphology MP:0005240
Genes (18)

Species:
human : 18
SpeciesGeneGeneIdGene NameEvidence
HumanBARHL2343472BarH-like homeobox 2
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanATOH7220202atonal homolog 7 (Drosophila)
INFERRED
HumanFOXN4121643forkhead box N4
INFERRED
HumanNEUROD458158neuronal differentiation 4
INFERRED
HumanDSCAML157453Down syndrome cell adhesion molecule like 1
INFERRED
HumanBHLHE2227319basic helix-loop-helix family, member e22
INFERRED
HumanAGTPBP123287ATP/GTP binding protein 1
INFERRED
HumanLAMC310319laminin, gamma 3
INFERRED
HumanGDF1110220growth differentiation factor 11
INFERRED
HumanPOU4F35459POU class 4 homeobox 3
INFERRED
HumanPOU4F25458POU class 4 homeobox 2
INFERRED
HumanNTRK24915neurotrophic tyrosine kinase, receptor, type 2
INFERRED
HumanLAMB23913laminin, beta 2 (laminin S)
INFERRED
HumanISL13670ISL LIM homeobox 1
INFERRED
HumanDSCAM1826Down syndrome cell adhesion molecule
INFERRED
HumanCDKN1B1027cyclin-dependent kinase inhibitor 1B (p27, Kip1)
INFERRED
HumanATRX546alpha thalassemia/mental retardation syndrome X-linked
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008104abnormal amacrine cell number0self