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TTR - transthyretin
- Synonym(s) : CTS, HsT2651
- Previous symbols and names : CTS1, PALB, carpal tunnel syndrome 1, prealbumin, amyloidosis type I
- Type : gene with protein product
- Chromosomal location : 18q12.1
- OMIM: 176300
- HGNC: 12405
- UniProtKB: P02766
- Genatlas: TTR
- GenCC: TTR
- Ensembl: ENSG00000118271
- IUPHAR-DB: 2851
- Reactome: P02766
- LOVD: TTR
Diseases list
- Disease-causing germline mutation(s) in ATTRV122I amyloidosis
ORPHA:85451 
- Disease-causing germline mutation(s) in ATTRV30M amyloidosis
ORPHA:85447 - Disease-causing germline mutation(s) in Euthyroid dysprealbuminemic hyperthyroxinemia
ORPHA:597939
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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