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Term:Turcot Syndrome
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Accession:DOID:9006244 term browser browse the term
Synonyms:exact_synonym: BTP1 SYNDROME;   BTPS1;   Brain Tumor-Polyposis Syndrome 1;   CHILDHOOD CANCER SYNDROME;   CMMRDS;   CNS tumors with Familial polyposis of the colon;   CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME;   MMR Deficiency;   MMRCS;   Mismatch Repair Cancer Syndrome;   Mismatch Repair Deficiency
 primary_id: MESH:C536928;   RDO:0002657
 alt_id: OMIM:276300
For additional species annotation, visit the Alliance of Genome Resources.

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Turcot Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Apc APC regulator of WNT signaling pathway JBrowse link 18 27,011,710 27,106,323 RGD:11554173
G Mlh1 mutL homolog 1 JBrowse link 8 119,486,655 119,523,716 RGD:7240710
G Msh2 mutS homolog 2 JBrowse link 6 11,215,951 11,274,916 RGD:7240710
G Msh6 mutS homolog 6 JBrowse link 6 11,644,565 11,662,389 RGD:7240710
G Pms2 PMS1 homolog 2, mismatch repair system component JBrowse link 12 12,714,394 12,738,654 RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15489
    syndrome 5228
      Turcot Syndrome 5
Path 2
Term Annotations click to browse term
  disease 15489
    disease of anatomical entity 14790
      gastrointestinal system disease 4483
        Gastrointestinal Diseases 2429
          intestinal disease 1404
            Intestinal Neoplasms 662
              Colorectal Neoplasms 642
                Turcot Syndrome 5
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.