Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

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 corpus callosum morphology
go back to main search page
Accession:MP:0000780 term browser browse the term
Definition:any structural anomaly of a thick bundle of nerve fibers comprising a commissural plate connecting the two cerebral hemispheres; it consists of contralateral axon projections that provides communications between the right and left cerebral hemispheres
Synonyms:narrow_synonym: corpus callosum dysplasia
 xref: HP:0001273



show annotations for term's descendants           Sort by:
abnormal corpus callosum morphology term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G L1cam L1 cell adhesion molecule IMP RGD PMID:30738385 RGD:14695001 NCBI chr  X:151,597,270...151,623,776
Ensembl chr  X:151,597,277...151,623,857
JBrowse link
abnormal corpus callosum size term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Csf1r colony stimulating factor 1 receptor IMP RGD PMID:33450391 RGD:126781687 NCBI chr18:56,834,152...56,860,804
Ensembl chr18:54,546,659...54,590,415
JBrowse link
G Csf1rtm(EGFP)Tset colony stimulating factor 1 receptor; target mutant, Tset IMP RGD PMID:33450391 RGD:126781687
decreased corpus callosum size term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Tmem67 transmembrane protein 67 IAGP RGD PMID:15052665 RGD:15014788 NCBI chr 5:30,333,793...30,386,702
Ensembl chr 5:25,536,458...25,589,334
JBrowse link
G Tmem67wpk transmembrane protein 67; wpk mutant IAGP RGD PMID:15052665 RGD:15014788

Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 5428
    nervous system phenotype 383
      abnormal nervous system morphology 220
        abnormal nervous system tract morphology 8
          abnormal brain commissure morphology 8
            abnormal dorsal telencephalic commissure morphology 8
              abnormal corpus callosum morphology 8
                abnormal corpus callosum average cell area + 0
                abnormal corpus callosum cell density + 0
                abnormal corpus callosum cell number + 0
                abnormal corpus callosum size + 6
                abnormal corpus callosum total cell area + 0
                absent corpus callosum 0
Path 2
Term Annotations click to browse term
  mammalian phenotype 5428
    nervous system phenotype 383
      abnormal nervous system morphology 220
        abnormal brain morphology 142
          abnormal brain white matter morphology 11
            abnormal brain commissure morphology 8
              abnormal dorsal telencephalic commissure morphology 8
                abnormal corpus callosum morphology 8
                  abnormal corpus callosum average cell area + 0
                  abnormal corpus callosum cell density + 0
                  abnormal corpus callosum cell number + 0
                  abnormal corpus callosum size + 6
                  abnormal corpus callosum total cell area + 0
                  absent corpus callosum 0
paths to the root