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MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.

Term:abnormal cued conditioning behavior
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Accession:MP:0001454 term browser browse the term
Definition:anomaly in the ability of an animal to learn and remember an association between an aversive experience (the unconditioned stimulus (US), usually a shock) and a neutral stimulus (the conditioned stimulus (CS), usually an auditory cue or light flash)
Synonyms:exact_synonym: abnormal context-trace conditioning;   abnormal cued conditioning behaviour;   cued conditioning anomalies;   cued fear conditioning abnormalities;   fear conditioning abnormalities
 alt_id: MP:0001453



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abnormal cued conditioning behavior term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gria2 glutamate ionotropic receptor AMPA type subunit 2 IMP RGD PMID:19160503 RGD:529195970 NCBI chr 2:168,247,490...168,367,616
Ensembl chr 2:165,947,521...166,069,510
JBrowse link
enhanced cued conditioning behavior term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Nr3c1 nuclear receptor subfamily 3, group C, member 1 sexual_dimorphism IMP associated with abnormal freezing behavior (MP:0020420); compared to female wild type littermate RGD PMID:31329100 RGD:407571699 NCBI chr18:31,522,783...31,644,508
Ensembl chr18:31,271,681...31,393,375
JBrowse link
G Nr3c1em1Kuan nuclear receptor subfamily 3, group C, member 1; CRISPR/Cas9 induced mutant1, Kuan sexual_dimorphism IMP associated with abnormal freezing behavior (MP:0020420); compared to female wild type littermate RGD PMID:31329100 RGD:407571699
impaired cued conditioning behavior term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Nrg1 neuregulin 1 IMP RGD PMID:23022220 RGD:39128254 NCBI chr16:65,954,084...67,007,484
Ensembl chr16:59,250,854...60,296,884
JBrowse link
G Nrg1Tn(sb-T2/Bart3)2.183Mcwi neuregulin 1; transposon insertion 2.183, Medical College of Wisconsin IMP RGD PMID:23022220 RGD:39128254

Term paths to the root
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Term Annotations click to browse term
  mammalian phenotype 5428
    behavior/neurological phenotype 618
      abnormal behavior 617
        abnormal cognition 127
          abnormal learning/memory/conditioning 124
            abnormal associative learning 41
              abnormal cued conditioning behavior 7
                enhanced cued conditioning behavior 3
                impaired cued conditioning behavior 3
paths to the root