GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version

Lists of Rare Genetic Disorders      

Familial Medullary Thyroid Carcinoma(Medullary thyroid carcinoma) 
An Autosomal dominant mode(s) within the Cancer disorders category
Reported Pathogenic variants
Candidate Gene Information
S.No. Name/GeneID Description Cytogentic Band Gene Location on genomic DNA Gene Length Exons Details Gene Cross-References
1 RET/5979 ret proto-oncogene 10q11.21 Chr10, NC_000010.11
(43077069..43130351)
53283 nt 20 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

2 NTRK1/4914 neurotrophic receptor tyrosine kinase 1 1q23.1 Chr1, NC_000001.11
(156815750..156881850)
66101 nt 19 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

Variant Information
Disorder Cross-References:      Orphanet          OMIM                    GTR          MedGen          MalaCards          EMBL-EBI OLS    Monarch Initiative          NORD     

Patient care services
Clinical Symptoms & Disabilities

Prevalence
Under development