Term:TARP Syndrome
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Accession:DOID:9005152 term browser browse the term
Definition:TARP syndrome is caused by hemizygous mutation in the RBM10 gene on chromosome Xp11. (OMIM)
Synonyms:exact_synonym: Pierre Robin syndrome with congenital heart malformation and clubfoot;   TARPS;   Talipes Equinovarus, Atrial Septal Defect, Robin Sequence, and Persistence of Left Superior Vena Cava
 primary_id: MESH:C536942;   RDO:0002670
 alt_id: OMIM:311900
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TARP Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rbm10 RNA binding motif protein 10 JBrowse link X 1,754,869 1,786,973 RGD:7240710

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Path 1
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  disease 14875
    syndrome 4220
      TARP Syndrome 1
Path 2
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  disease 14875
    Developmental Diseases 7711
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6750
        Congenital Abnormalities 3150
          Musculoskeletal Abnormalities 1191
            Congenital Limb Deformities 343
              Lower Extremity Deformities, Congenital 75
                Congenital Foot Deformities 68
                  Talipes 41
                    clubfoot 31
                      TARP Syndrome 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.