RHEB - Ras homolog, mTORC1 binding Gene

Also Known as RHEB2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6009

About RHEB

Cytogenetic location: 7q36.1 Genomic coordinates (GRCh38): 7:151,466,012-151,519,895 (from NCBI)

This gene has 7 transcripts (splice variants), 123 orthologues and 35 paralogues. Ubiquitous expression in adrenal (RPKM 38.1), brain (RPKM 36.3) and 25 other tissues.

Summary

This gene is a member of the small GTPase superfamily and encodes a lipid-anchored, cell membrane protein with five repeats of the RAS-related GTP-binding region. This protein is vital in regulation of growth and cell cycle progression due to its role in the Insulin/TOR/S6K signaling pathway. The protein has GTPase activity and shuttles between a GDP-bound form and a GTP-bound form, and farnesylation of the protein is required for this activity. Three pseudogenes have been mapped, two on chromosome 10 and one on chromosome 22. [provided by RefSeq, Jul 2008]

RHEB Products (1)

mRNA Protein Name
NM_005614.4 NP_005605.1 GTP-binding protein Rheb
Molecular Function GO Annotation Evidence References Source
enables GDP binding IMP
IMP: Inferred from mutant phenotype
15728574 GOA
enables GTP binding IMP
IMP: Inferred from mutant phenotype
15728574 GOA
enables GTPase activity IDA
IDA: Inferred from direct assay
15340059 GOA
enables magnesium ion binding IMP
IMP: Inferred from mutant phenotype
15728574 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17301792 GOA
enables protein kinase activator activity IDA
IDA: Inferred from direct assay
29236692 GOA
enables protein serine/threonine kinase activator activity IDA
IDA: Inferred from direct assay
15854902 GOA
Biological Process GO Annotation Evidence References Source
involved in cellular response to nutrient levels IDA
IDA: Inferred from direct assay
29236692 GOA
involved in positive regulation of TOR signaling IMP
IMP: Inferred from mutant phenotype
20381137 GOA
involved in positive regulation of TORC1 signaling IDA
IDA: Inferred from direct assay
12172553 GOA
involved in regulation of type B pancreatic cell development IMP
IMP: Inferred from mutant phenotype
19258434 GOA
Cellular Component GO Annotation Evidence References Source
is active in endomembrane system IDA
IDA: Inferred from direct assay
22002721 GOA
is active in lysosomal membrane IDA
IDA: Inferred from direct assay
24529379 GOA
is active in postsynaptic density EXP
EXP: Inferred from Experiment
27898073 GOA
is active in postsynaptic density IDA
IDA: Inferred from direct assay
27898073 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

RHEB Protein Structure

Ras

Ras: Ras family (8 - 167)

  • 0
  • 100
  • 184 a.a.
Protein Preferred Names Protein Names

GTP-binding protein Rheb

  • Ras homolog enriched in brain 2

RHEB Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
RHEB Q15382 TPT1 Homo sapiens P13693 17301792
Intra
RHEB Q15382 TPT1 Homo sapiens P13693 17301792
Intra
RHEB Q15382 LAMP2 Homo sapiens P13473-2 28514442
Intra
RHEB Q15382 q9y649_human Homo sapiens Q9Y649 32814053
Intra
RHEB Q15382 q9y649_human Homo sapiens Q9Y649 32814053
Intra
RHEB Q15382 q9y649_human Homo sapiens Q9Y649 32814053
Intra
RHEB Q15382 PLD1 Homo sapiens Q13393 18550814
Intra
RHEB Q15382 FGFR3 Homo sapiens P22607 32814053
Intra
RHEB Q15382 FGFR3 Homo sapiens P22607 32814053
Intra
RHEB Q15382 FGFR3 Homo sapiens P22607 32814053
Intra
RHEB Q15382 MTOR Homo sapiens P42345 18550814
Intra
RHEB Q15382 MTOR Homo sapiens P42345 16098514
Intra
RHEB Q15382 CCK Homo sapiens P06307 32814053
Intra
RHEB Q15382 APPBP2 Homo sapiens Q92624 32296183
Intra
RHEB Q15382 APPBP2 Homo sapiens Q92624 32296183
Intra
RHEB Q15382 APPBP2 Homo sapiens Q92624 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant RHEB Proteins

Cat. No. Product Name Accession Purity
HY-P71260 RHEB Protein, Human (GST) Q15382 (M1-M184) ≥ 90%, as determined by reducing SDS-PAGE.
HY-P700268 RHEB Protein, Human (sf9, N-His) Q15382 (M1-C181) ≥ 85%, as determined by reducing SDS-PAGE.

RHEB Antibodies

Cat. No. Product Name Application Reactivity
HY-P80310 RHEB Antibody (YA094) WB, ICC/IF, IHC-P, FC Human, Mouse

Related Diseases

Diseases Alias
Tuberous Sclerosis
  • Tuberous Sclerosis Syndrome

  • Bourneville'S Disease

  • Epiloia

  • Cerebral Sclerosis

  • Tuberose Sclerosis

  • Tuberous Sclerosis 1

  • Bourneville Disease

  • Bourneville Phakomatosis

  • Pringle'S Disease

Hemimegalencephaly
  • Unilateral Megalencephaly

  • Macrencephaly

Renal Cell Carcinoma, Papillary, 1
  • Papillary Renal Cell Carcinoma

  • Hereditary Papillary Renal Cell Carcinoma

  • Papillary Renal Cell Carcinoma, Sporadic

  • Papillary Renal Cell Adenocarcinoma

  • RCCP

  • RCCP1

  • Renal Cell Carcinoma, Papillary

  • Renal Cell Carcinoma, Papillary, 1, Familial And Somatic

  • Chromophil Carcinoma Of Kidney

  • Papillary Kidney Carcinoma

  • Sporadic Papillary Renal Cell Carcinoma

  • Chromophil Renal Cell Carcinoma

  • Papillary Renal Carcinoma, Malignant -

  • Papillary Renal Cell Carcinoma, Bilateral -

  • Papillary Renal Cell Carcinoma, Familial -

  • Papillary Renal Cell Carcinoma, Multiple -

  • Papillary Renal Cell Carcinoma, Sporadic -

  • Renal Adenocarcinoma

  • Chromophil Rcc

  • Hprcc

  • Renal Cell Carcinoma Papillary

  • Chromophilic Renal Cell Carcinoma

  • Prcc

  • Carcinoma, Renal Cell, Papillary, Type 1

  • Type 1 Papillary Renal Cell Carcinoma

  • Renal Cell Carcinoma

  • Hereditary Papillary Renal Carcinoma

Bladder Urothelial Carcinoma
  • Bladder Transitional Cell Carcinoma

  • Transitional Cell Carcinoma Of Bladder

  • Transitional Cell Carcinoma Of The Bladder

  • Urinary Bladder Urothelial Carcinoma

  • Urothelial Bladder Carcinoma

  • Carcinoma Transitional Cell Bladder

  • Tcc - [Transitional Cell Carcinoma] Of Bladder

Renal Cell Carcinoma, Nonpapillary
  • Renal Cell Carcinoma

  • RCC

  • Nonpapillary Renal Cell Carcinoma

  • Clear Cell Renal Cell Carcinoma

  • Hypernephroma

  • Adenocarcinoma Of Kidney

  • Renal Carcinoma, Chromophobe, Somatic

  • Clear Cell Carcinoma Of Kidney

  • Clear-Cell Metastatic Renal Cell Carcinoma

  • Clear Cell Renal Carcinoma

  • Renal Cell Carcinoma, Somatic

  • Conventional Renal Cell Carcinoma

  • Conventional Renal Cell Carcinoma

  • Renal Clear Cell Carcinoma

  • Ccrcc

  • Hereditary Clear Cell Renal Cell Carcinoma

  • Carcinoma, Renal Cell

  • Renal Cell Carcinoma, Clear Cell, Somatic

  • Renal Cell Carcinoma, Clear Cell

  • Clear Cell Kidney Carcinoma

  • Clear Cell Rcc

  • Cystic-Multilocular Variant

  • Clear Cell Renal Cell Adenocarcinoma

  • Hereditary Clear Cell Renal Cell Adenocarcinoma

  • Common Renal Cell Carcinoma

  • Crcc

  • Renal Cell Carcinoma Non-Papillary

  • Carcinoma Renal Cell

  • Renal Cell Cancer

  • Carcinoma, Renal Cell, Nonpapillary

Kidney Angiomyolipoma
  • Angiomyolipoma Of Kidney

  • Renal Angiomyolipoma

Subependymal Glioma
  • Mixed Subependymoma-Ependymoma

  • Subependymal Astrocytoma

  • Who Grade I Ependymal Tumor

  • Glioma, Subependymal

Benign Ependymoma
  • Ependymoma

  • Epithelial Ependymoma

  • Who Grade Ii Ependymal Tumor

  • Myxopapillary Ependymoma

Kidney Benign Neoplasm
  • Renal And Ureteral Tumor

  • Benign Kidney Neoplasm

Subependymal Giant Cell Astrocytoma
  • Sega

  • Astrocytoma Subependymal Giant Cell

  • Subependymal Giant-Cell Astrocytoma

Neurodegeneration With Brain Iron Accumulation
  • Nbia

  • Neurodegeneration With Brain Iron Accumulation Disorders

  • Neurodegeneration, With Brain Iron Accumulation

Cowden Syndrome 1
  • Bannayan-Riley-Ruvalcaba Syndrome

  • Pten Hamartoma Tumor Syndrome

  • Lhermitte-Duclos Disease

  • Bannayan-Zonana Syndrome

  • Phts

  • Riley-Smith Syndrome

  • Bzs

  • Ruvalcaba-Myhre-Smith Syndrome

  • Multiple Hamartoma Syndrome

  • Rmss

  • Brrs

  • Dysplastic Gangliocytoma Of The Cerebellum

  • CWS1

  • Cs

  • Cd

  • Mham

  • Pten Hamartoma Tumor Syndrome With Granular Cell Tumor

  • Macrocephaly Multiple Lipomas And Hemangiomata

  • Bannayan-Ruvalcaba-Riley Syndrome

  • Myhre-Riley-Smith Syndrome

  • LDD

  • Cerebelloparenchymal Disorder Vi

  • Hamartoma Syndrome, Multiple

  • Bbrs

  • Macrocephaly, Pseudopapilledema, And Multiple Hemangiomata

  • Macrocephaly, Multiple Lipomas, And Hemangiomata

  • Macrocephaly Pseudopapilledema And Multiple Hemangiomas

  • Ruvalcaba -Myhre-Smith Syndrome

  • Ruvalcaba-Myhre Syndrome

  • Cowden Disease

  • Macrocephaly Pseudopapilledema And Multiple Hemangiomata

  • Cerebellar Granule Cell Hypertrophy And Megalencephaly

  • Cpd6

  • Pten Hamartoma Tumor Syndromes

  • Cowden Syndrome, Type 1

Fragile X Syndrome
  • FXS

  • Martin-Bell Syndrome

  • Fraxa Syndrome

  • Marker X Syndrome

  • X-Linked Mental Retardation And Macroorchidism

  • Fragile X Mental Retardation Syndrome

  • Fra Syndrome

  • Mental Retardation, X-Linked, Associated With Marxq28

  • X-Linked Intellectual Disability And Macroorchidism

  • Frax Syndrome

  • Symptomatic Form Of Fragile X Syndrome In Female Carriers

  • Fragile-X Syndrome

  • Fraxe Syndrome

Proteus Syndrome
  • Proteus Syndrome, Somatic

  • Partial Gigantism-Nevi-Hemihypertrophy-Macrocephaly Syndrome

  • Gigantism, Partial, Of Hands And Feet, Nevi, Hemihypertrophy, And Macrocephaly

  • Wiedemann'S Syndrome

  • Hemihypertrophy And Macrocephaly

  • Partial Gigantism Of Hands And Feet, Nevi, Hemihypertrophy, Macrocephaly

  • Ps

  • PROTEUSS

  • Partial Gigantism Of Hands And Feet Nevi Hemihypertrophy And Macrocephaly

Autism Spectrum Disorder
  • Asd

  • Autism Spectrum Disorders

  • Autistic Continuum

  • Pervasive Developmental Disorder

  • Pervasive Development Disorder

  • Autistic Behavior

  • Autistic Disorder

  • Autistic

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Childhood Autism

  • Kanner Syndrome

  • Pervasive Developmental Delay Nos

  • Pervasive Developmental Disorder, Not Otherwise Specified

Cowden Syndrome
  • Cowden Disease

  • Multiple Hamartoma Syndrome

  • Cowden'S Disease

  • Lhermitte-Duclos Disease

  • Cd

  • Cs

  • Mham

  • Dysplastic Gangliocytoma Of Cerebellum

  • Cowden'S Syndrome

  • Hamartoma Syndrome, Multiple

Autism
  • Autistic Disorder

  • Autism Susceptibility 1

  • Childhood Autism

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Kanner'S Syndrome

  • Autistic

Rasopathy
  • Ras/Mitogen-Activated Protein Kinase Syndrome

Type 2 Diabetes Mellitus
  • Insulin Resistance

  • NIDDM

  • Type 2 Diabetes

  • Diabetes Mellitus, Non-Insulin-Dependent

  • T2D

  • Noninsulin-Dependent Diabetes Mellitus

  • Diabetes Mellitus, Type Ii

  • Maturity-Onset Diabetes

  • Insulin Resistance, Severe, Digenic

  • Diabetes Mellitus, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent

  • Diabetes Mellitus, Noninsulin-Dependent, Association With

  • Diabetes Mellitus, Noninsulin-Dependent, Late Onset

  • Hypertension, Insulin Resistance-Related, Susceptibility To

  • Insulin Resistance, Susceptibility To

  • Non-Insulin-Dependent Diabetes Mellitus

  • Type Ii Diabetes Mellitus

  • Adult-Onset Diabetes Mellitus

  • Maturity-Onset Diabetes Mellitus

  • Diabetes Mellitus Type 2

  • Type Ii Diabetes

  • Type 2 Diabetes Mellitus, Susceptibility To

  • Diabetes, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Type 2, Susceptibility To

  • Diabetes Mellitus, Noninsulin-Dependent, 2

  • Diabetes Mellitus, Type Ii, Susceptibility To

  • Hypertension, Insulin Resistance-Related

  • Adult-Onset Diabetes

  • Aodm

  • Diabetes Mellitus, Adult-Onset

  • Diabetes Mellitus Type Ii

  • Diabetes Mellitus Type 2, Susceptibility To

  • Diabetes, Type Ii, Susceptibility To

  • Diabetes Type 2

  • Diabetes Mellitus

  • Adult Onset Diabetes

  • Maturity Onset Diabetes

  • Nonketotic Diabetes

  • Non-Insulin Dependent Diabetes Mellitus

  • T2dm - [Type 2 Diabetes Mellitus]

  • Niddm - [Non Insulin Dependent Diabetes Mellitus]

  • Dm2

  • Dm Type Ii

  • Diabetic Type 2

  • Insulin Requiring Type 2 Diabetes

  • Noninsulin Dependent Diabetes

  • Non-Insulin-Dependent Diabetes Mellitus Without Complications

  • Diabetes Due To Insulin Secretory Defect

  • Diabetes Mellitus Due To Insulin Secretory Defect

  • Non-Insulin-Dependent Diabetes Of The Young

  • Senile Diabetes

  • Nonketotic Hyperglycaemia

  • Stable Diabetes

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus RHEB RGD RGD:621840
Mus musculus RHEB MGD MGI:97912
Bos taurus RHEB VGNC VGNC:33939
Felis catus RHEB VGNC VGNC:64609
Canis familiaris RHEB VGNC VGNC:45551
Others RHEB NCBI