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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 mechanical nociception
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Accession:MP:0002734 term browser browse the term
Definition:abnormal capability to sense pain elicited by mechanical stimulation
Synonyms:exact_synonym: mechanical nociception abnormalities
 alt_id: MP:0002737


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abnormal mechanical nociception term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cacna1f calcium voltage-gated channel subunit alpha1 F IAGP DNA:mutation:cds: c.2941C>T RGD PMID:22800190 RGD:13792551 NCBI chr  X:14,868,096...14,896,413
Ensembl chr  X:14,868,024...14,896,413 		JBrowse link
G Cacna1f csnb calcium voltage-gated channel subunit alpha1 F; congenital stationary night blindness mutant IAGP DNA:mutation:cds: c.2941C>T RGD PMID:22800190 RGD:13792551
decreased mechanical nociceptive threshold term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gla galactosidase, alpha IMP RGD PMID:29563343 RGD:150429980 NCBI chr  X:97,769,227...97,780,646
Ensembl chr  X:97,768,996...97,780,664 		JBrowse link
G Glaem2Mcwi galactosidase, alpha; CRISPR/Cas9 system induced mutant 2, Medical College of Wisconsin IMP compared to wild type RGD PMID:29563343 RGD:150429980
G Oprl1 opioid related nociceptin receptor 1 IMP RGD PMID:25704616 RGD:14349028 NCBI chr 3:168,831,934...168,839,920
Ensembl chr 3:168,834,003...168,839,920 		JBrowse link
G Oprl1m1Hubr opioid related nociceptin receptor 1; ENU induced mutant1, Hubr IMP RGD PMID:25704616 RGD:14349028
increased mechanical nociceptive threshold term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G C3 complement C3 induced IMP RGD PMID:29695418 PMID:29695418 RGD:19165124, RGD:19165124 NCBI chr 9:2,087,437...2,114,366
Ensembl chr 9:2,087,437...2,114,429 		JBrowse link
G C3em1Linf complement C3; CRISPR/Cas9 system induced mutant 1, Linf induced IMP RGD PMID:29695418 PMID:29695418 RGD:19165124, RGD:19165124
G Fcgr1a Fc gamma receptor 1A IMP RGD PMID:32510872 RGD:127338469 NCBI chr 2:183,851,075...183,860,077
Ensembl chr 2:183,851,077...183,859,994 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 5402
    behavior/neurological phenotype 594
      abnormal behavior 593
        abnormal sensory capabilities/reflexes/nociception 76
          abnormal touch/ nociception 38
            abnormal mechanical nociception 14
              absent mechanical nociception 0
              decreased mechanical nociceptive threshold 6
              increased mechanical nociceptive threshold 5
paths to the root