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Aliases for TTR Gene

Aliases for TTR Gene

  • Transthyretin 2 3 3 5
  • Prealbumin, Amyloidosis Type I 2 3
  • PALB 3 4
  • ATTR 3 4
  • TBPA 3 4
  • Epididymis Luminal Protein 111 3
  • Thyroxine-Binding Prealbumin 3
  • Carpal Tunnel Syndrome 1 2
  • Prealbumin 4
  • HsT2651 3
  • HEL111 3
  • CTS1 3
  • CTS 3

External Ids for TTR Gene

Previous HGNC Symbols for TTR Gene

  • PALB
  • CTS1

Previous GeneCards Identifiers for TTR Gene

  • GC18P029194
  • GC18P028991
  • GC18P027423
  • GC18P027425
  • GC18P026028

Summaries for TTR Gene

Entrez Gene Summary for TTR Gene

  • This gene encodes one of the three prealbumins, which include alpha-1-antitrypsin, transthyretin and orosomucoid. The encoded protein, transthyretin, is a homo-tetrameric carrier protein, which transports thyroid hormones in the plasma and cerebrospinal fluid. It is also involved in the transport of retinol (vitamin A) in the plasma by associating with retinol-binding protein. The protein may also be involved in other intracellular processes including proteolysis, nerve regeneration, autophagy and glucose homeostasis. Mutations in this gene are associated with amyloid deposition, predominantly affecting peripheral nerves or the heart, while a small percentage of the gene mutations are non-amyloidogenic. The mutations are implicated in the etiology of several diseases, including amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis and carpal tunnel syndrome. [provided by RefSeq, Aug 2017]

GeneCards Summary for TTR Gene

TTR (Transthyretin) is a Protein Coding gene. Diseases associated with TTR include Amyloidosis, Hereditary, Transthyretin-Related and Hyperthyroxinemia, Dystransthyretinemic. Among its related pathways are HIV Life Cycle and Metabolism. Gene Ontology (GO) annotations related to this gene include identical protein binding and hormone activity.

UniProtKB/Swiss-Prot for TTR Gene

  • Thyroid hormone-binding protein. Probably transports thyroxine from the bloodstream to the brain.

Gene Wiki entry for TTR Gene

Additional gene information for TTR Gene

No data available for CIViC summary , Tocris Summary , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for TTR Gene

Genomics for TTR Gene

GeneHancer (GH) Regulatory Elements for TTR Gene

Promoters and enhancers for TTR Gene
GeneHancer (GH) Identifier GH Type GH
GH Sources Gene Association Score Total Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor
Binding Sites
Gene Targets
GH18J031591 Promoter/Enhancer 1.4 EPDnew ENCODE 650.7 +0.4 350 1.4 ELF3 FOXA2 ARID4B RAD21 RARA ETS1 YY1 CREM MIXL1 HMG20B TTR GC18M031541
GH18J031677 Promoter/Enhancer 2.4 EPDnew Ensembl ENCODE dbSUPER 10.3 +90.7 90740 10.1 PKNOX1 FOXA2 ARNT ZNF133 SIN3A ZNF48 GLIS2 ZNF207 ZNF143 FOS B4GALT6 TTR GC18P031684 ENSG00000259985 GC18M031541
GH18J031565 Enhancer 0.8 ENCODE 12.4 -25.1 -25126 1.8 ELF3 FOXA2 DMAP1 THRB RAD21 RARA CREM RXRA MXD4 REST TTR B4GALT6 SLC25A52 TRAPPC8 DSG2 DSG2-AS1 GC18M031541
GH18J031632 Enhancer 0.9 ENCODE dbSUPER 11 +42.6 42624 3.1 HDGF MEIS2 PKNOX1 EBF1 IRF4 FOSL1 POLR2A EED CBFA2T2 ATF7 TTR GC18M031541 GC18P031684 B4GALT6
GH18J031738 Enhancer 0.9 ENCODE 10.3 +147.2 147208 1.1 PKNOX1 ATF1 FOXA2 ARNT ARID4B YY1 NCOA2 ZNF280A TCF12 ZNF766 TTR LOC390846 GC18M031760
- Elite GeneHancer and/or Elite GeneHancer-gene association Download GeneHancer data from 2017 publication | Request up-to-date GeneHancer data (full dataset)

GeneHancers around TTR on UCSC Golden Path with GeneCards custom track

Top Transcription factor binding sites by QIAGEN in the TTR gene promoter:
  • deltaCREB
  • CREB
  • MEF-2
  • aMEF-2
  • MEF-2A
  • Meis-1
  • Meis-1b
  • Meis-1a

Genomic Locations for TTR Gene

Genomic Locations for TTR Gene
7,299 bases
Plus strand
7,299 bases
Plus strand

Genomic View for TTR Gene

Genes around TTR on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
TTR Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for TTR Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for TTR Gene

Proteins for TTR Gene

  • Protein details for TTR Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Recommended name:
    Protein Accession:
    Secondary Accessions:
    • Q549C7
    • Q6IB96
    • Q9UBZ6
    • Q9UCM9

    Protein attributes for TTR Gene

    147 amino acids
    Molecular mass:
    15887 Da
    Quaternary structure:
    • Homotetramer. Dimer of dimers. In the homotetramer, subunits assemble around a central channel that can accommodate two ligand molecules. Interacts with RBP4.
    • Tetramer dissociation and partial unfolding leads to the formation of aggregates and amyloid fibrils. Small molecules that occupy at least one of the thyroid hormone binding sites stabilize the tetramer, and thereby stabilize the native state and protect against misfolding and the formation of amyloid fibrils.
    • Two binding sites for thyroxine are located in the channel. Less than 1% of plasma prealbumin molecules are normally involved in thyroxine transport. L-thyroxine binds to the transthyretin by an order of magnitude stronger than does the triiodo-L-thyronine. Thyroxine-binding globulin is the major carrier protein for thyroid hormones in man.
    • About 40% of plasma transthyretin circulates in a tight protein-protein complex with the plasma retinol-binding protein (RBP). The formation of the complex with RBP stabilizes the binding of retinol to RBP and decreases the glomerular filtration and renal catabolism of the relatively small RBP molecule. There is evidence for 2 binding sites for RBP, one possibly being a region that includes Ile-104, located on the outer surface of the transthyretin molecule.

    Three dimensional structures from OCA and Proteopedia for TTR Gene

neXtProt entry for TTR Gene

Post-translational modifications for TTR Gene

  • Not glycosylated under normal conditions. Following unfolding, caused for example by variant AMYL-TTR Gly-38, the cryptic Asn-118 site is exposed and glycosylated by STT3B-containing OST complex, leading to its degradation by the ER-associated degradation (ERAD) pathway.
  • Glycosylation at posLast=118118
  • Modification sites at PhosphoSitePlus

Other Protein References for TTR Gene

ENSEMBL proteins:
REFSEQ proteins:

Antibody Products

  • R&D Systems Antibodies for TTR (Transthyretin/Prealbumin)

No data available for DME Specific Peptides for TTR Gene

Domains & Families for TTR Gene

Gene Families for TTR Gene

Human Protein Atlas (HPA):
  • Cancer-related genes
  • Disease related genes
  • Plasma proteins
  • Predicted secreted proteins

Suggested Antigen Peptide Sequences for TTR Gene

GenScript: Design optimal peptide antigens:

Graphical View of Domain Structure for InterPro Entry



  • Each monomer has two 4-stranded beta sheets and the shape of a prolate ellipsoid. Antiparallel beta-sheet interactions link monomers into dimers. A short loop from each monomer forms the main dimer-dimer interaction. These two pairs of loops separate the opposed, convex beta-sheets of the dimers to form an internal channel.
  • Belongs to the transthyretin family.
  • Each monomer has two 4-stranded beta sheets and the shape of a prolate ellipsoid. Antiparallel beta-sheet interactions link monomers into dimers. A short loop from each monomer forms the main dimer-dimer interaction. These two pairs of loops separate the opposed, convex beta-sheets of the dimers to form an internal channel.
  • Belongs to the transthyretin family.
genes like me logo Genes that share domains with TTR: view

Function for TTR Gene

Molecular function for TTR Gene

UniProtKB/Swiss-Prot Function:
Thyroid hormone-binding protein. Probably transports thyroxine from the bloodstream to the brain.
GENATLAS Biochemistry:
transthyretin (prealbumin)

Phenotypes From GWAS Catalog for TTR Gene

Gene Ontology (GO) - Molecular Function for TTR Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005179 hormone activity IEA --
GO:0005515 protein binding IPI 986177
GO:0042562 hormone binding IEA --
GO:0042802 identical protein binding IPI 19861125
GO:0046982 protein heterodimerization activity IEA --
genes like me logo Genes that share ontologies with TTR: view
genes like me logo Genes that share phenotypes with TTR: view

Human Phenotype Ontology for TTR Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Models for TTR Gene

MGI Knock Outs for TTR:
  • Ttr Ttr<tm1Wsb>
  • Ttr Ttr<tm1Kymm>

Animal Model Products

CRISPR Products

Inhibitory RNA Products

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for TTR

No data available for Enzyme Numbers (IUBMB) , Transcription Factor Targets and HOMER Transcription for TTR Gene

Localization for TTR Gene

Subcellular locations from UniProtKB/Swiss-Prot for TTR Gene

Secreted. Cytoplasm.

Subcellular locations from

Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for TTR gene
Compartment Confidence
extracellular 5
lysosome 5
cytosol 3
plasma membrane 2
cytoskeleton 2
nucleus 2
endoplasmic reticulum 2
mitochondrion 1
peroxisome 1
golgi apparatus 1
endosome 1

Subcellular locations from the

Human Protein Atlas (HPA)
  • Golgi apparatus (2)
See all subcellular structures

Gene Ontology (GO) - Cellular Components for TTR Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005576 extracellular region TAS,IEA --
GO:0005615 extracellular space IBA,IEA --
GO:0005737 cytoplasm IEA --
GO:0032991 protein-containing complex IEA --
GO:0035578 azurophil granule lumen TAS --
genes like me logo Genes that share ontologies with TTR: view

Pathways & Interactions for TTR Gene

genes like me logo Genes that share pathways with TTR: view

Pathways by source for TTR Gene

Gene Ontology (GO) - Biological Process for TTR Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0001523 retinoid metabolic process TAS --
GO:0006144 NOT purine nucleobase metabolic process IBA --
GO:0010469 regulation of signaling receptor activity IEA --
GO:0030198 extracellular matrix organization TAS --
GO:0042572 retinol metabolic process IEA --
genes like me logo Genes that share ontologies with TTR: view

No data available for SIGNOR curated interactions for TTR Gene

Drugs & Compounds for TTR Gene

(118) Drugs for TTR Gene - From: DrugBank, ClinicalTrials, DGIdb, HMDB, and Novoseek

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
Levothyroxine Approved Pharma Carrier 0
Liothyronine Approved, Vet_approved Pharma Carrier 0
Diclofenac Approved, Vet_approved Pharma Channel blocker, Antagonist, Inhibition, Inhibitor, Carrier 340
Diethylstilbestrol Approved, Investigational Pharma Antagonist, Agonist, Carrier 5
Diflunisal Approved, Investigational Pharma Carrier 4

(47) Additional Compounds for TTR Gene - From: Novoseek

Name Synonyms Role CAS Number PubChem IDs PubMed IDs
genes like me logo Genes that share compounds with TTR: view

Transcripts for TTR Gene

mRNA/cDNA for TTR Gene

(1) REFSEQ mRNAs :
(14) Additional mRNA sequences :
(2837) Selected AceView cDNA sequences:
(5) Ensembl transcripts including schematic representations, and UCSC links where relevant :

Unigene Clusters for TTR Gene

Representative Sequences:

CRISPR Products

Inhibitory RNA Products

  • Search GeneCopoeia for shRNA, lentivirus and/or AAV clone products for TTR

Alternative Splicing Database (ASD) splice patterns (SP) for TTR Gene

ExUns: 1a · 1b ^ 2a · 2b ^ 3a · 3b ^ 4a · 4b
SP1: -
SP3: - -

Relevant External Links for TTR Gene

GeneLoc Exon Structure for
ECgene alternative splicing isoforms for

Expression for TTR Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for TTR Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

mRNA differential expression in normal tissues according to GTEx for TTR Gene

This gene is overexpressed in Liver (x39.2) and Pancreas (x4.2).

Protein differential expression in normal tissues from HIPED for TTR Gene

This gene is overexpressed in Cerebrospinal fluid (19.0), Plasma (11.2), and Serum (7.0).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB and MOPED for TTR Gene

Protein tissue co-expression partners for TTR Gene

- Elite partner

NURSA nuclear receptor signaling pathways regulating expression of TTR Gene:


SOURCE GeneReport for Unigene cluster for TTR Gene:


mRNA Expression by UniProt/SwissProt for TTR Gene:

Tissue specificity: Detected in serum and cerebrospinal fluid (at protein level). Highly expressed in choroid plexus epithelial cells. Detected in retina pigment epithelium and liver.

Evidence on tissue expression from TISSUES for TTR Gene

  • Liver(5)
  • Pancreas(5)
  • Nervous system(5)
  • Eye(4.8)
  • Blood(4.7)
  • Bone marrow(4.3)
  • Thyroid gland(3.3)
  • Intestine(3.2)
  • Kidney(3.2)
  • Heart(3)
  • Muscle(3)
  • Skin(2.3)
  • Lung(2.2)
  • Spleen(2.2)
  • Stomach(2.1)
  • Urine(2.1)

Phenotype-based relationships between genes and organs from Gene ORGANizer for TTR Gene

Germ Layers:
  • ectoderm
  • endoderm
  • mesoderm
  • cardiovascular
  • digestive
  • immune
  • nervous
  • reproductive
  • skeletal muscle
  • skeleton
  • urinary
Head and neck:
  • brain
  • cerebrospinal fluid
  • cranial nerve
  • ear
  • eye
  • head
  • meninges
  • neck
  • esophagus
  • heart
  • heart valve
  • intestine
  • kidney
  • large intestine
  • small intestine
  • stomach
  • penis
  • prostate
  • rectum
  • urinary bladder
  • arm
  • digit
  • finger
  • foot
  • forearm
  • hand
  • lower limb
  • toe
  • upper limb
  • blood vessel
  • peripheral nerve
  • peripheral nervous system
  • spinal cord
genes like me logo Genes that share expression patterns with TTR: view

Orthologs for TTR Gene

This gene was present in the common ancestor of animals.

Orthologs for TTR Gene

Organism Taxonomy Gene Similarity Type Details
(Pan troglodytes)
Mammalia TTR 34 33
  • 98.19 (n)
(Canis familiaris)
Mammalia TTR 34 33
  • 87.3 (n)
(Bos Taurus)
Mammalia TTR 34 33
  • 85.84 (n)
(Rattus norvegicus)
Mammalia Ttr 33
  • 82.31 (n)
(Mus musculus)
Mammalia Ttr 16 34 33
  • 81.86 (n)
(Monodelphis domestica)
Mammalia TTR 34
  • 70 (a)
(Ornithorhynchus anatinus)
Mammalia TTR 34
  • 66 (a)
(Gallus gallus)
Aves TTR 34 33
  • 73.47 (n)
(Anolis carolinensis)
Reptilia TTR 34
  • 63 (a)
tropical clawed frog
(Silurana tropicalis)
Amphibia ttr 33
  • 66.93 (n)
African clawed frog
(Xenopus laevis)
Amphibia LOC397787 33
(Danio rerio)
Actinopterygii ttr 34 33
  • 58.6 (n)
fruit fly
(Drosophila melanogaster)
Insecta CG30016 34
  • 25 (a)
(Caenorhabditis elegans)
Secernentea R09H10.3 34
  • 28 (a)
ZK697.8 34
  • 25 (a)
Species where no ortholog for TTR was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • baker's yeast (Saccharomyces cerevisiae)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rainbow trout (Oncorhynchus mykiss)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea squirt (Ciona intestinalis)
  • sea squirt (Ciona savignyi)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • wheat (Triticum aestivum)

Evolution for TTR Gene

Gene Tree for TTR (if available)
Gene Tree for TTR (if available)
Evolutionary constrained regions (ECRs) for TTR: view image

Paralogs for TTR Gene

(2) SIMAP similar genes for TTR Gene using alignment to 4 proteins:

  • Q13736_HUMAN
  • Q13739_HUMAN
genes like me logo Genes that share paralogs with TTR: view

No data available for Paralogs for TTR Gene

Variants for TTR Gene

Sequence variations from dbSNP and Humsavar for TTR Gene

SNP ID Clin Chr 18 pos Variation AA Info Type
rs104894664 pathogenic, Amyloidogenic transthyretin amyloidosis 31,592,959(+) G/A coding_sequence_variant, missense_variant
rs104894665 pathogenic, Amyloidogenic transthyretin amyloidosis, AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED, Amyloidosis, transthyretin-related (AMYL-TTR) [MIM:105210] 31,593,017(+) T/C coding_sequence_variant, missense_variant
rs112263266 not-provided, benign, not specified, Cardiomyopathy 31,598,547(+) TCTGTCTGTCT/TCTGTCT intron_variant
rs11541790 conflicting-interpretations-of-pathogenicity, uncertain-significance, not provided, Amyloidogenic transthyretin amyloidosis, Amyloidosis, transthyretin-related (AMYL-TTR) [MIM:105210] 31,592,956(+) C/T coding_sequence_variant, missense_variant
rs11541796 pathogenic, Amyloidogenic transthyretin amyloidosis, Amyloidosis, transthyretin-related (AMYL-TTR) [MIM:105210], Amyloidosis, transthyretin-related (AMYL-TTR) [MIM:105210] 31,593,011(+) A/G coding_sequence_variant, missense_variant

Structural Variations from Database of Genomic Variants (DGV) for TTR Gene

Variant ID Type Subtype PubMed ID
nsv1066881 CNV gain 25217958
nsv576636 CNV loss 21841781
nsv833615 CNV gain 17160897

Variation tolerance for TTR Gene

Residual Variation Intolerance Score: 72.7% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 2.18; 39.52% of all genes are more intolerant (likely to be disease-causing)

Additional Variant Information for TTR Gene

Human Gene Mutation Database (HGMD)
SNPedia medical, phenotypic, and genealogical associations of SNPs for

SNP Genotyping and Copy Number Assay Products

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for TTR Gene

Disorders for TTR Gene

MalaCards: The human disease database

(73) MalaCards diseases for TTR Gene - From: HGMD, OMIM, ClinVar, GTR, Orphanet, Swiss-Prot, DISEASES, Novoseek, and GeneCards

Disorder Aliases PubMed IDs
amyloidosis, hereditary, transthyretin-related
  • hereditary amyloidosis, transthyretin-related
hyperthyroxinemia, dystransthyretinemic
  • dttrh
carpal tunnel syndrome
  • cts1
atrial standstill 1
  • atrst1
  • amyloid disease
- elite association - COSMIC cancer census association via MalaCards
Search TTR in MalaCards View complete list of genes associated with diseases


  • Amyloidosis, transthyretin-related (AMYL-TTR) [MIM:105210]: A hereditary generalized amyloidosis due to transthyretin amyloid deposition. Protein fibrils can form in different tissues leading to amyloid polyneuropathies, amyloidotic cardiomyopathy, carpal tunnel syndrome, systemic senile amyloidosis. The disease includes leptomeningeal amyloidosis that is characterized by primary involvement of the central nervous system. Neuropathologic examination shows amyloid in the walls of leptomeningeal vessels, in pia arachnoid, and subpial deposits. Some patients also develop vitreous amyloid deposition that leads to visual impairment (oculoleptomeningeal amyloidosis). Clinical features include seizures, stroke-like episodes, dementia, psychomotor deterioration, variable amyloid deposition in the vitreous humor. {ECO:0000269 PubMed:10036587, ECO:0000269 PubMed:10071047, ECO:0000269 PubMed:10211412, ECO:0000269 PubMed:10436378, ECO:0000269 PubMed:10439117, ECO:0000269 PubMed:10611950, ECO:0000269 PubMed:10627135, ECO:0000269 PubMed:10694917, ECO:0000269 PubMed:10842705, ECO:0000269 PubMed:10842718, ECO:0000269 PubMed:10882995, ECO:0000269 PubMed:11243784, ECO:0000269 PubMed:11445644, ECO:0000269 PubMed:11866053, ECO:0000269 PubMed:12050338, ECO:0000269 PubMed:12403615, ECO:0000269 PubMed:12557757, ECO:0000269 PubMed:12771253, ECO:0000269 PubMed:1301926, ECO:0000269 PubMed:1351039, ECO:0000269 PubMed:1362222, ECO:0000269 PubMed:1436517, ECO:0000269 PubMed:1517749, ECO:0000269 PubMed:1520326, ECO:0000269 PubMed:1520336, ECO:0000269 PubMed:15214015, ECO:0000269 PubMed:15217993, ECO:0000269 PubMed:1544214, ECO:0000269 PubMed:15478468, ECO:0000269 PubMed:1570831, ECO:0000269 PubMed:15735344, ECO:0000269 PubMed:16185074, ECO:0000269 PubMed:1656975, ECO:0000269 PubMed:16627944, ECO:0000269 PubMed:1734866, ECO:0000269 PubMed:17453626, ECO:0000269 PubMed:17503405, ECO:0000269 PubMed:17577687, ECO:0000269 PubMed:17635579, ECO:0000269 PubMed:19167329, ECO:0000269 PubMed:1932142, ECO:0000269 PubMed:2046936, ECO:0000269 PubMed:2161654, ECO:0000269 PubMed:23317988, ECO:0000269 PubMed:2363717, ECO:0000269 PubMed:2891727, ECO:0000269 PubMed:3022108, ECO:0000269 PubMed:3135807, ECO:0000269 PubMed:3722385, ECO:0000269 PubMed:3818577, ECO:0000269 PubMed:6487335, ECO:0000269 PubMed:6583672, ECO:0000269 PubMed:6651852, ECO:0000269 PubMed:7655883, ECO:0000269 PubMed:7850982, ECO:0000269 PubMed:7910950, ECO:0000269 PubMed:7914929, ECO:0000269 PubMed:7923855, ECO:0000269 PubMed:8019560, ECO:0000269 PubMed:8038017, ECO:0000269 PubMed:8081397, ECO:0000269 PubMed:8095302, ECO:0000269 PubMed:8133316, ECO:0000269 PubMed:8257997, ECO:0000269 PubMed:8352764, ECO:0000269 PubMed:8382610, ECO:0000269 PubMed:8428915, ECO:0000269 PubMed:8579098, ECO:0000269 PubMed:8990019, ECO:0000269 PubMed:9066351, ECO:0000269 PubMed:9605286, ECO:0000269 PubMed:9733771, ECO:0000269 Ref.90}. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • Hyperthyroxinemia, dystransthyretinemic (DTTRH) [MIM:145680]: A condition characterized by elevation of total and free thyroxine in healthy, euthyroid persons without detectable binding protein abnormalities. {ECO:0000269 PubMed:1979335}. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • Carpal tunnel syndrome 1 (CTS1) [MIM:115430]: A condition characterized by entrapment of the median nerve within the carpal tunnel. Symptoms include burning pain and paresthesias involving the ventral surface of the hand and fingers which may radiate proximally. Impairment of sensation in the distribution of the median nerve and thenar muscle atrophy may occur. This condition may be associated with repetitive occupational trauma, wrist injuries, amyloid neuropathies, rheumatoid arthritis. {ECO:0000269 PubMed:8309582}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Additional Disease Information for TTR

Genetic Association Database
Human Genome Epidemiology Navigator
ATLAS of Genetics and Cytogenetics in Oncology and Haematology
genes like me logo Genes that share disorders with TTR: view

No data available for Genatlas for TTR Gene

Publications for TTR Gene

  1. A new mutant transthyretin (Arg 10) associated with familial amyloid polyneuropathy. (PMID: 1362222) Uemichi T … Benson MD (Journal of medical genetics 1992) 3 4 22 44 58
  2. A novel transthyretin mutation at position 30 (Leu for Val) associated with familial amyloidotic polyneuropathy. (PMID: 1520326) Murakami T … Ando M (Biochemical and biophysical research communications 1992) 3 4 22 44 58
  3. A new transthyretin mutation associated with amyloid cardiomyopathy. (PMID: 1570831) Saraiva MJ … Goodman DS (American journal of human genetics 1992) 3 4 22 44 58
  4. Positive association between ALDH1A2 and schizophrenia in the Chinese population. (PMID: 19703508) Wan C … He L (Progress in neuro-psychopharmacology & biological psychiatry 2009) 3 22 44 58
  5. Complement C1Q polymorphisms modulate onset in familial amyloidotic polyneuropathy TTR Val30Met. (PMID: 19493541) Dardiotis E … Kyriakides T (Journal of the neurological sciences 2009) 3 22 44 58

Products for TTR Gene

  • Addgene plasmids for TTR

Sources for TTR Gene

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