RET

GENERAL INFORMATION

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Gene name

RET

Gene description

Ret proto-oncogene

Protein class

Cancer-related genes
Disease related genes
Enzymes
FDA approved drug targets
Plasma proteins
Predicted membrane proteins
Predicted secreted proteins

Predicted localization

Membrane,Secreted

Number of transcripts

4
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (adrenal gland)
GTEx:Mixed

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic and membranous expression at variable levels in most tissues.

ANTIBODY RELIABILITY

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Data reliability
description

Secreted protein, tissue location of RNA and protein might differ and correlation is complex. Pending retesting.

Data reliability

Uncertain based on 3 antibodies.
HPA008356 , CAB002581 , CAB018342
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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

Adrenal gland

Lymph node

Liver

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 (adrenal gland)

Organ

Expression

GTEx dataset
RNA tissue category:  Mixed

Organ

Expression



GENE INFORMATION

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Gene name

RET (HGNC Symbol)

Synonyms

CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1, PTC, RET51

Description

Ret proto-oncogene (HGNC Symbol)

Entrez gene summary

This gene, a member of the cadherin superfamily, encodes one of the receptor tyrosine kinases, which are cell-surface molecules that transduce signals for cell growth and differentiation. This gene plays a crucial role in neural crest development, and it can undergo oncogenic activation in vivo and in vitro by cytogenetic rearrangement. Mutations in this gene are associated with the disorders multiple endocrine neoplasia, type IIA, multiple endocrine neoplasia, type IIB, Hirschsprung disease, and medullary thyroid carcinoma. Two transcript variants encoding different isoforms have been found for this gene. Additional transcript variants have been described but their biological validity has not been confirmed. [provided by RefSeq, Jul 2008]

Chromosome

10

Cytoband

q11.21

Chromosome location (bp)

43077027 - 43130351

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000165731 (version 78.38)

Entrez gene

5979

UniProt

P07949 (UniProt - Evidence at protein level)

neXtProt

NX_P07949

Antibodypedia

RET antibodies


PROTEIN BROWSER

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ENST00000340058
 
ENST00000355710
 
ENST00000498820
 
ENST00000615310
 
 
 
 


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)

RET-001 ENSP00000347942
ENST00000355710
P07949
Show all »
Show » Show » 1114 124.3 Yes 1
RET-002 ENSP00000344798
ENST00000340058
P07949
Show all »
Show » Show » 1072 119.8 Yes 1
RET-003 ENSP00000419080
ENST00000498820
C9JYL6
Show all »
Show » 181 19.4 Yes 1
RET-201 ENSP00000480088
ENST00000615310
Q9BTX6
Show all »
Show » Show » 458 51.2 Yes 0