Send us a Message

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


The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories ( For more information about these ontologies, see the MGI Publications Page at

Term:hindlimb paralysis
go back to main search page
Accession:MP:0000755 term browser browse the term
Definition:severe or complete loss of power of voluntary movement in the muscles of the hindlimb through injury or disease of it or its nerve supply
Synonyms:exact_synonym: hind limb paralysis

show annotations for term's descendants           Sort by:
hindlimb paralysis term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atm ATM serine/threonine kinase IMP DNA:deletion:exon: RGD PMID:27895165 PMID:28007901 RGD:12879393, RGD:12879399 NCBI chr 8:53,828,741...53,932,773
Ensembl chr 8:53,831,093...53,932,437
JBrowse link
G Atmem1Kyo ATM serine/threonine kinase; ZFN induced mutant 1, Kyo IMP RGD PMID:28007901 RGD:12879399
G Atmm1Kyo ATM serine/threonine kinase; ENU induced mutant 1, Kyo IMP RGD PMID:27895165 PMID:28007901 RGD:12879393, RGD:12879399

Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 5415
    behavior/neurological phenotype 603
      abnormal behavior 602
        abnormal motor capabilities/coordination/movement 240
          abnormal voluntary movement 169
            paralysis 12
              limb paralysis 8
                hindlimb paralysis 8
paths to the root