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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 Abcg4 ATP binding cassette subfamily G member 4 JBrowse link 8 48,604,915 48,626,219 RGD:8554872
G Arcn1 archain 1 JBrowse link 8 49,051,257 49,075,861 RGD:8554872
G Atp5mg ATP synthase membrane subunit g JBrowse link 8 49,220,441 49,227,273 RGD:8554872
G Bcl9l BCL9 like JBrowse link 8 48,805,684 48,835,794 RGD:8554872
G C2cd2l C2CD2-like JBrowse link 8 48,641,792 48,652,119 RGD:8554872
G Cbl Cbl proto-oncogene JBrowse link 8 48,481,256 48,564,775 RGD:8554872
G Ccdc153 coiled-coil domain containing 153 JBrowse link 8 48,570,718 48,577,856 RGD:8554872
G Ccdc84 coiled-coil domain containing 84 JBrowse link 8 48,729,695 48,736,574 RGD:8554872
G Cd3d CD3d molecule JBrowse link 8 49,282,502 49,287,095 RGD:8554872
G Cd3e CD3e molecule JBrowse link 8 49,297,604 49,309,370 RGD:8554872
G Cd3g CD3g molecule JBrowse link 8 49,274,553 49,280,943 RGD:8554872
G Cxcr5 C-X-C motif chemokine receptor 5 JBrowse link 8 48,835,688 48,852,032 RGD:8554872
G Ddx6 DEAD-box helicase 6 JBrowse link 8 48,924,768 48,961,394 RGD:8554872
G Dpagt1 dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 JBrowse link 8 48,657,779 48,664,531 RGD:8554872
G Foxr1 forkhead box R1 JBrowse link 8 48,754,300 48,762,765 RGD:8554872
G H2ax H2A.X variant histone JBrowse link 8 48,665,652 48,666,981 RGD:8554872
G Hinfp histone H4 transcription factor JBrowse link 8 48,626,398 48,638,012 RGD:8554872
G Hmbs hydroxymethylbilane synthase JBrowse link 8 48,667,278 48,674,673 RGD:8554872
G Hyou1 hypoxia up-regulated 1 JBrowse link 8 48,699,796 48,711,912 RGD:8554872
G Ift46 intraflagellar transport 46 JBrowse link 8 49,075,978 49,097,689 RGD:8554872
G Jaml junction adhesion molecule like JBrowse link 8 49,378,644 49,408,894 RGD:8554872
G Kmt2a lysine methyltransferase 2A JBrowse link 8 49,110,407 49,185,872 RGD:8554872
G Mpzl2 myelin protein zero-like 2 JBrowse link 8 49,342,067 49,353,080 RGD:8554872
G Mpzl3 myelin protein zero-like 3 JBrowse link 8 49,354,257 49,374,444 RGD:8554872
G Nlrx1 NLR family member X1 JBrowse link 8 48,583,559 48,600,203 RGD:8554872
G Pdzd3 PDZ domain containing 3 JBrowse link 8 48,577,905 48,582,353 RGD:8554872
G Phldb1 pleckstrin homology-like domain, family B, member 1 JBrowse link 8 48,997,189 49,045,176 RGD:8554872
G Rps25 ribosomal protein s25 JBrowse link 8 48,727,346 48,729,722 RGD:8554872
G Scn2b sodium voltage-gated channel beta subunit 2 JBrowse link 8 49,419,003 49,431,110 RGD:8554872
G Scn4b sodium voltage-gated channel beta subunit 4 JBrowse link 8 49,441,106 49,456,279 RGD:7240710
RGD:8554872
G Slc37a4 solute carrier family 37 member 4 JBrowse link 8 48,716,914 48,723,024 RGD:8554872
G Tmem25 transmembrane protein 25 JBrowse link 8 49,100,759 49,106,258 RGD:8554872
G Trappc4 trafficking protein particle complex 4 JBrowse link 8 48,723,755 48,727,182 RGD:8554872
G Treh trehalase JBrowse link 8 48,983,802 48,998,072 RGD:8554872
G Ttc36 tetratricopeptide repeat domain 36 JBrowse link 8 49,106,374 49,109,981 RGD:8554872
G Ube4a ubiquitination factor E4A JBrowse link 8 49,229,713 49,271,894 RGD:8554872
G Upk2 uroplakin 2 JBrowse link 8 48,772,906 48,774,898 RGD:8554872
G Vps11 VPS11 core subunit of CORVET and HOPS complexes JBrowse link 8 48,677,492 48,692,295 RGD:8554872
Familial Atrial Fibrillation 17 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:8554872

Term paths to the root
Path 1
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  disease 15590
    syndrome 5131
      long QT syndrome 213
        long QT syndrome 10 38
          Familial Atrial Fibrillation 17 1
Path 2
Term Annotations click to browse term
  disease 15590
    Developmental Diseases 8723
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7503
        genetic disease 6993
          monogenic disease 4551
            autosomal genetic disease 3501
              autosomal dominant disease 2065
                long QT syndrome 10 38
                  Familial Atrial Fibrillation 17 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.