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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 sensory neuron morphology
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Accession:MP:0000965 term browser browse the term
Definition:any structural anomaly of cells that innervate an effector (muscle or glandular) tissue and are responsible for transmission of sensory impulses
Synonyms:exact_synonym: abnormal sensory neurons


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abnormal sensory neuron morphology term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gla galactosidase, alpha IMP compared to wild type RGD PMID:29563343 PMID:34541380 RGD:150429980, RGD:401976419 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 PMID:34541380 RGD:150429980, RGD:401976419
abnormal retina horizontal cell morphology 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 (rat) RGD PMID:22634626 RGD:13782386 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 (rat) RGD PMID:22634626 RGD:13782386
photoreceptor outer segment degeneration term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Tmem67 transmembrane protein 67 IAGP RGD PMID:23516626 RGD:11535084 NCBI chr 5:25,536,458...25,589,378
Ensembl chr 5:25,536,458...25,589,334 		JBrowse link
retina photoreceptor degeneration term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Myo15a myosin XVA induces IAGP DNA:missense mutation:cds:exon 56 T>C, p.Leu3157Pro (rat)
compared to LEW/Ztm		 RGD PMID:21479269 PMID:21479269 RGD:150429616, RGD:150429616 NCBI chr10:45,277,619...45,335,953
Ensembl chr10:45,278,737...45,335,340 		JBrowse link
G Myo15aci2 myosin XVA; ci2 mutant induces IAGP compared to LEW/Ztm RGD PMID:21479269 RGD:150429616
G Pde6b phosphodiesterase 6B IMP compared to wild-type RGD PMID:31009522 RGD:40924664 NCBI chr14:1,323,310...1,366,450
Ensembl chr14:1,323,310...1,366,450 		JBrowse link
G Pde6bem1Baek phosphodiesterase 6B; Cpf1-CRISPR induced mutant1, Baek IMP compared to wild-type RGD PMID:31009522 RGD:40924664
Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 5422
    nervous system phenotype 380
      abnormal nervous system morphology 217
        abnormal neuron morphology 71
          abnormal sensory neuron morphology 19
            abnormal amacrine cell morphology + 0
            abnormal chemoreceptor morphology + 0
            abnormal nociceptor morphology 0
            abnormal olfactory bulb interneuron morphology + 1
            abnormal parasympathetic neuron morphology 0
            abnormal polymodal receptor morphology 0
            abnormal proprioceptive neuron morphology + 0
            abnormal retina bipolar cell morphology + 1
            abnormal retina ganglion cell morphology + 0
            abnormal retina horizontal cell morphology + 4
            abnormal retina photoreceptor morphology + 10
            abnormal sensory neuron innervation pattern + 0
            abnormal sympathetic neuron morphology + 0
            abnormal thermoreceptor morphology 0
            decreased sensory neuron number + 2
            increased sensory neuron number + 0
Path 2
Term Annotations click to browse term
  mammalian phenotype 5422
    nervous system phenotype 380
      abnormal nervous system morphology 217
        abnormal somatic nervous system morphology 36
          abnormal somatic sensory system morphology 22
            abnormal sensory neuron morphology 19
              abnormal amacrine cell morphology + 0
              abnormal chemoreceptor morphology + 0
              abnormal nociceptor morphology 0
              abnormal olfactory bulb interneuron morphology + 1
              abnormal parasympathetic neuron morphology 0
              abnormal polymodal receptor morphology 0
              abnormal proprioceptive neuron morphology + 0
              abnormal retina bipolar cell morphology + 1
              abnormal retina ganglion cell morphology + 0
              abnormal retina horizontal cell morphology + 4
              abnormal retina photoreceptor morphology + 10
              abnormal sensory neuron innervation pattern + 0
              abnormal sympathetic neuron morphology + 0
              abnormal thermoreceptor morphology 0
              decreased sensory neuron number + 2
              increased sensory neuron number + 0
paths to the root