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ONTOLOGY REPORT - ANNOTATIONS


Term:long QT syndrome 10
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Accession:DOID:0110651 term browser browse the term
Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3. (DO)
Synonyms:exact_synonym: LQT10
 primary_id: MESH:C567514
 alt_id: OMIM:611819;   RDO:0015574
 xref: GARD:10436
For additional species annotation, visit the Alliance of Genome Resources.


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long QT syndrome 10 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Scn4b sodium voltage-gated channel beta subunit 4 JBrowse link 8 49,441,106 49,456,279 RGD:7240710
RGD:8554872
Familial Atrial Fibrillation 17 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Pex12 peroxisomal biogenesis factor 12 JBrowse link 10 70,512,785 70,516,494 RGD:11554173

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  disease 14759
    syndrome 4210
      long QT syndrome 177
        long QT syndrome 10 2
          Familial Atrial Fibrillation 17 1
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  disease 14759
    Developmental Diseases 7628
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6666
        Congenital Abnormalities 3137
          Cardiovascular Abnormalities 781
            congenital heart disease 730
              long QT syndrome 177
                long QT syndrome 10 2
                  Familial Atrial Fibrillation 17 1
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