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ONTOLOGY REPORT - ANNOTATIONS


Term:hereditary spastic paraplegia 61
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Accession:DOID:0110812 term browser browse the term
Definition:A hereditary spastic paraplegia that has_material_basis_in mutation in the ARL6IP1 gene on chromosome 16p12. (DO)
Synonyms:exact_synonym: SPG61;   autosomal recessive spastic paraplegia 61;   autosomal recessive spastic paraplegia type 61;   spastic paraplegia-61
 primary_id: OMIM:615685
 alt_id: RDO:9001113
 xref: ORDO:401780
For additional species annotation, visit the Alliance of Genome Resources.


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hereditary spastic paraplegia 61 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Arl6ip1 ADP-ribosylation factor like GTPase 6 interacting protein 1 JBrowse link 1 187,770,160 187,779,675 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      nervous system disease 10216
        central nervous system disease 8092
          paraplegia 131
            hereditary spastic paraplegia 117
              hereditary spastic paraplegia 61 1
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      nervous system disease 10216
        central nervous system disease 8092
          neurodegenerative disease 2691
            Nervous System Heredodegenerative Disorders 1718
              motor peripheral neuropathy 457
                hereditary spastic paraplegia 117
                  hereditary spastic paraplegia 61 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.