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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 cranial nerve morphology
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Accession:MP:0001056 term browser browse the term
Definition:any structural anomaly of any of the twelve nerves that emerge from the cranium as opposed to the spinal nerves
Synonyms:exact_synonym: abnormal cranial nerves;   cranial nerve abnormalities
 narrow_synonym: cranial nerve dysplasia
 xref: HP:0001291



show annotations for term's descendants           Sort by:
abnormal abducens nerve morphology term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Pax6 paired box 6 IAGP RGD PMID:9247338 RGD:731242 NCBI chr 3:112,590,034...112,611,771
Ensembl chr 3:92,135,637...92,157,014
JBrowse link
G Pax6Sey2 paired box gene 6, small eye mutation 2 IAGP RGD PMID:9247338 RGD:731242
abnormal hypoglossal nerve morphology term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Pax6 paired box 6 IAGP RGD PMID:9247338 RGD:731242 NCBI chr 3:112,590,034...112,611,771
Ensembl chr 3:92,135,637...92,157,014
JBrowse link
G Pax6Sey2 paired box gene 6, small eye mutation 2 IAGP RGD PMID:9247338 RGD:731242
optic nerve atrophy term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Wfs1 wolframin ER transmembrane glycoprotein onset IMP RGD PMID:28860598 RGD:149735331 NCBI chr14:78,035,205...78,059,718
Ensembl chr14:73,810,404...73,835,602
JBrowse link
G Wfs1em1Ptsn wolframin ER transmembrane glycoprotein; ZFN induced mutant 1 onset IMP RGD PMID:28860598 RGD:149735331

Term paths to the root
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Term Annotations click to browse term
  mammalian phenotype 5428
    nervous system phenotype 383
      abnormal nervous system morphology 220
        abnormal somatic nervous system morphology 36
          abnormal cranial nerve morphology 7
            abnormal abducens nerve morphology + 3
            abnormal accessory nerve morphology 0
            abnormal facial nerve morphology + 0
            abnormal glossopharyngeal nerve morphology + 0
            abnormal hypoglossal nerve morphology + 3
            abnormal oculomotor nerve morphology + 0
            abnormal olfactory nerve morphology + 0
            abnormal optic nerve morphology + 4
            abnormal trigeminal nerve morphology + 0
            abnormal trochlear nerve morphology + 0
            abnormal vagus nerve morphology + 0
            abnormal vestibulocochlear nerve morphology + 0
paths to the root