TTR

GENERAL INFORMATION

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Gene name

TTR

Gene description

Transthyretin

Protein class

Cancer-related genes
Disease related genes
Plasma proteins
Predicted secreted proteins

Predicted localization

Secreted

Number of transcripts

3
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (liver)
GTEx:Tissue enriched (liver)

Protein evidence

Evidence at protein level

Protein localization

Selective expression in pancreatic islets, renal tubules and liver. Positivity also observed in plasma.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data. Secreted protein, tissue location of RNA and protein might differ and correlation is complex.

Data reliability

Supportive based on 4 antibodies.
HPA002550 , CAB002517 , CAB062567 , CAB073406
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Pancreas

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enriched (liver)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (liver)

Organ

Expression



GENE INFORMATION

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Gene name

TTR (HGNC Symbol)

Synonyms

CTS, CTS1, HsT2651, PALB

Description

Transthyretin (HGNC Symbol)

Entrez gene summary

This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein; it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported; most mutations are related to amyloid deposition, affecting predominantly peripheral nerve and/or the heart, and a small portion of the gene mutations is non-amyloidogenic. The diseases caused by mutations include amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis, carpal tunnel syndrome, etc. [provided by RefSeq, Jan 2009]

Chromosome

18

Cytoband

q12.1

Chromosome location (bp)

31591726 - 31599021

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000118271 (version 78.38)

Entrez gene

7276

UniProt

P02766 (UniProt - Evidence at protein level)

neXtProt

NX_P02766

Antibodypedia

TTR antibodies


PROTEIN BROWSER

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ENST00000237014
 
ENST00000610404
 
ENST00000613781
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

TTR-001 ENSP00000237014
ENST00000237014
P02766
Show all »
Show » Show » 147 15.9 Yes 0
TTR-201 ENSP00000477599
ENST00000610404
Show » 185 20.1 Yes 0
TTR-202 ENSP00000479174
ENST00000613781
A6XMH1
Show all »
Show » 139 15.1 Yes 0