REST - RE1 silencing transcription factor Gene

Also Known as WT6; XBR; HGF5; NRSF; DFNA27; GINGF5

生物種: Homo sapiens

遺伝子タイプ: protein coding
遺伝子ID: 5978

About REST

Cytogenetic location: 4q12 Genomic coordinates (GRCh38): 4:56,907,900-56,935,844 (from NCBI)

This gene has 12 transcripts (splice variants), 226 orthologues, 29 paralogues and is associated with 5 phenotypes. Ubiquitous expression in bone marrow (RPKM 9.2), testis (RPKM 8.5) and 25 other tissues.

Summary

This gene was initially identified as a transcriptional repressor that represses neuronal genes in non-neuronal tissues. However, depending on the cellular context, this gene can act as either an oncogene or a tumor suppressor. The encoded protein is a member of the Kruppel-type zinc finger transcription factor family. It represses transcription by binding a DNA sequence element called the neuron-restrictive silencer element. The protein is also found in undifferentiated neuronal progenitor cells and it is thought that this repressor may act as a master negative regulator of neurogenesis. Alternatively spliced transcript variants have been described. [provided by RefSeq, May 2018]

REST Products (3)

mRNA Protein Name
NM_001193508.1 NP_001180437.1 RE1-silencing transcription factor
NM_001363453.2 NP_001350382.1 RE1-silencing transcription factor
NM_005612.5 NP_005603.3 RE1-silencing transcription factor
Biological Process GO Annotation Evidence 参考文献 由来
involved in cellular response to electrical stimulus IMP
IMP: Inferred from mutant phenotype
18570921 GOA
involved in cellular response to glucocorticoid stimulus IDA
IDA: Inferred from direct assay
17984088 GOA
involved in cellular response to xenobiotic stimulus IMP
IMP: Inferred from mutant phenotype
20564196 GOA
involved in negative regulation by host of viral transcription IDA
IDA: Inferred from direct assay
17555596 GOA
involved in negative regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
7697725 GOA
involved in negative regulation of DNA-templated transcription IMP
IMP: Inferred from mutant phenotype
18570921 GOA
involved in negative regulation of aldosterone biosynthetic process IMP
IMP: Inferred from mutant phenotype
19342457 GOA
involved in negative regulation of amniotic stem cell differentiation IMP
IMP: Inferred from mutant phenotype
20942606 GOA
involved in negative regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
20564196 GOA
involved in negative regulation of cortisol biosynthetic process IMP
IMP: Inferred from mutant phenotype
19342457 GOA
involved in negative regulation of gene expression IMP
IMP: Inferred from mutant phenotype
20564196 GOA
involved in negative regulation of insulin secretion IMP
IMP: Inferred from mutant phenotype
20942606 GOA
involved in negative regulation of mesenchymal stem cell differentiation IMP
IMP: Inferred from mutant phenotype
18570921 GOA
involved in negative regulation of miRNA transcription IMP
IMP: Inferred from mutant phenotype
33108349 GOA
involved in negative regulation of neuron differentiation IDA
IDA: Inferred from direct assay
21258371 GOA
involved in negative regulation of neuron differentiation IMP
IMP: Inferred from mutant phenotype
18570921 GOA
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
8568247 GOA
involved in nervous system process IMP
IMP: Inferred from mutant phenotype
24670762 GOA
involved in positive regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
17984088 GOA
involved in positive regulation of apoptotic process IMP
IMP: Inferred from mutant phenotype
20564196 GOA
involved in positive regulation of cysteine-type endopeptidase activity involved in apoptotic process IMP
IMP: Inferred from mutant phenotype
20564196 GOA
involved in positive regulation of stem cell population maintenance IDA
IDA: Inferred from direct assay
21258371 GOA
involved in regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
11779185 GOA
involved in response to hypoxia IDA
IDA: Inferred from direct assay
27531581 GOA
Cellular Component GO Annotation Evidence 参考文献 由来
located in cytoplasm IDA
IDA: Inferred from direct assay
24670762 GOA
located in nucleus IDA
IDA: Inferred from direct assay
7697725 GOA
located in nucleus IMP
IMP: Inferred from mutant phenotype
16442230 GOA
part of transcription repressor complex IDA
IDA: Inferred from direct assay
10734093 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

REST Protein Structure

zf-C2H2_4

zf-C2H2_4: C2H2-type zinc finger (217 - 238)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (290 - 313)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (318 - 343)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (348 - 370)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1097 a.a.
Protein Preferred Names Protein Names

RE1-silencing transcription factor

  • neural-restrictive silencer factor

REST Protein-protein interaction Information

Type
タンパク質名 Protein ID Interactor Interactor Species Interactor ID Detection Method 参考文献
Intra
REST Q13127 KDM5C Homo sapiens P41229 17468742
Intra
REST Q13127 HSP90AA1 Homo sapiens P07900 31361762
Intra
REST Q13127 HSP90AA1 Homo sapiens P07900
Y2H
31361762
Intra
REST Q13127 HSP90AA1 Homo sapiens P07900 31361762
Intra
REST Q13127 BTRC Homo sapiens Q9Y297 18354483
Intra
REST Q13127 BTRC Homo sapiens Q9Y297 18354483
Intra
REST Q13127 BTRC Homo sapiens Q9Y297 18354483
Intra
REST Q13127 BTRC Homo sapiens Q9Y297 18354482
Intra
REST Q13127 FBXW11 Homo sapiens Q9UKB1 18354483
Intra
REST Q13127 FBXW11 Homo sapiens Q9UKB1 18354482
Cross: Cross-species interaction Intra: Intraspecies interaction

REST 抗体

製品番号 製品名 アプリケーション 反応性
HY-P83635 REST Antibody (YA3380) WB Human

関連疾患

Diseases Alias
Fibromatosis, Gingival, 5
  • GINGF5

  • Ggf5

  • Fibromatosis, Gingival, Hereditary, 5

  • Hgf5

  • Gingival Fibromatosis 5

Wilms Tumor 6
  • WT6

  • Wilms Tumor 6, Susceptibility To

  • Susceptibility To Wilms Tumor 6

  • Wilms Tumor, Susceptibility To

  • Nephroblastoma

Deafness, Autosomal Dominant 27
  • DFNA27

  • Autosomal Dominant Nonsyndromic Deafness 27

  • Autosomal Dominant Deafness 27

  • Deafness, Autosomal Dominant, 27

Gingival Fibromatosis
  • Hereditary Gingival Fibromatosis

  • Hereditary Gingival Hyperplasia

  • Autosomal Dominant Gingival Fibromatosis

  • Autosomal Dominant Gingival Hyperplasia

  • Fibromatosis, Gingival, Hereditary

  • Fibromatosis, Gingival

Fibromatosis, Gingival, 1
  • GINGF1

  • Ggf1

  • Fibromatosis, Gingival, Hereditary

  • Hgf

  • Hereditary Gingival Fibromatosis

  • Gingf

  • Gingival Fibromatosis, 1

  • Fibromatosis Gingival, Hereditary, 1

  • Hgf1

  • Hereditary Gingival Fibromatosis, 1

Wilms Tumor Predisposition
Aging
Wilms Tumor 1
  • Nephroblastoma

  • Wilms Tumor

  • WT1

  • Wilms' Tumor

  • Bilateral Wilms Tumor

  • Wilms Tumor, Type 1

  • Wilms Tumor, Somatic

  • Adult Nephroblastoma

  • Wt1 Disorder

  • Renal Embryonic Tumor

  • Adult Kidney Wilms Tumor

  • Childhood Kidney Wilms Tumor

  • Nonanaplastic Kidney Wilms Tumor

Fibromatosis
Prostate Neuroendocrine Neoplasm
  • Neuroendocrine Tumor Of The Prostate

Ischemia
  • Acute Coronary Syndrome

Medulloblastoma
  • MDB

  • Cpnet

  • Localized Primitive Neuroectodermal Tumor

  • Classic Medulloblastoma

  • Medulloblastoma Predisposition Syndrome

  • Medulloblastoma, Somatic

  • Brain Medulloblastoma

  • Cns Pnet

  • Infratentorial Primitive Neuroectodermal Tumor

  • Neuroectodermal Tumors, Primitive

  • Medulloblastomas

  • Desmoplastic Medulloblastoma

  • Medulloblastoma, With Extensive Nodularity

  • Medulloblastoma Of Unspecified Site

  • Medullomyoblastoma Of Unspecified Site

Rett Syndrome
  • Atypical Rett Syndrome

  • RTT

  • Rett Disorder

  • Rts

  • Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use

  • Rett Syndrome, Preserved Speech Variant

  • Rett Syndrome, Atypical

  • Rett'S Disorder

  • Rett Syndrome Variant

  • Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome

  • Cerebroatrophic Hyperammonemia

  • Rett Like Syndrome

  • Rett'S Syndrome

  • Atypical Rtt

  • Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use

  • Rett Syndrome Preserved Speech Variant

  • Rett Syndrome Zappella Variant

  • Rett Syndrome, Zappella Variant

Down Syndrome
  • Trisomy 21

  • Complete Trisomy 21 Syndrome

  • Down'S Syndrome

  • Trisomy 21 Syndrome

  • Down'S Syndrome - Trisomy 21

  • Downs Syndrome

  • G Trisomy

  • 47,Xx,+21

  • 47,Xy,+21

  • Trisomy G

  • Down Syndrome, Susceptibility To

  • Chromosome 21 Trisomy

  • Trisomy 21 Nos

  • Abnormal Autosomes 21

Breast Cancer
  • Breast Carcinoma

  • Male Breast Cancer

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Frontotemporal Dementia
  • Pallidopontonigral Degeneration

  • Frontotemporal Lobar Degeneration

  • Semantic Dementia

  • FTD

  • Frontotemporal Lobe Dementia

  • Multiple System Tauopathy With Presenile Dementia

  • Dementia, Frontotemporal

  • Frontotemporal Dementia With Parkinsonism

  • Mstd

  • Frontotemporal Lobar Degeneration With Tau Inclusions

  • Ftld With Tau Inclusions

  • Dementia, Frontotemporal, With Parkinsonism

  • Fldem

  • Ftdp17

  • Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

  • Ddpac

  • Wilhelmsen-Lynch Disease

  • Wld

  • Ppnd

  • Dementia, Frontotemporal, With Or Without Parkinsonism

  • Semantic Primary Progressive Aphasia

  • Semantic Variant Ppa

  • Wilhemsen-Lynch Disease

  • Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

  • Ftd-Als

  • Ftld

  • Pick Complex

  • Pick Disease Of The Brain

  • Frontotemporal Dementia With Parkinsonism-17

  • Grn-Related Frontotemporal Dementia

  • Frontotemporal Dementia With Motor Neuron Disease

  • Dementia In Fronto-Temporal Lobar Degeneration

  • Ftd - [Frontotemporal Dementia]

  • Temple Dementia

  • Frontal Lobe Dementia

Major Depressive Disorder
  • Seasonal Affective Disorder

  • Unipolar Depression

  • Depression

  • MDD

  • Depressive Disorder

  • Unipolar Depression, Susceptibility To

  • Major Depressive Disorder 1

  • Major Depressive Disorder, Response To Citalopram Therapy In

  • Major Depressive Disorder 2

  • Winter Depression

  • Single Major Depressive Episode

  • Sad

  • Clinical Depression

  • Major Depression

  • Depressive Syndrome

  • Major Depressive Disorder And Accelerated Response To Antidepressant Drug Treatment

  • Seasonal Affective Disorder, Susceptibility To

  • Recurrent Major Depression

  • Affective Disorder, Seasonal

  • Depression In A Seasonal Pattern

  • Depression

  • Seasonal

  • Major Depressive Disorder With A Seasonal Pattern

  • Seasonal Depression

  • Seasonal Mood Disorder

  • Mental Depression

  • Recurrent Major Depressive Episodes

Neuroblastoma
  • Nb

  • Neuroblastoma, Susceptibility To

  • Neuroblastomas

  • Central Neuroblastoma

Sensorineural Hearing Loss
  • Sensory Hearing Loss

  • Sensorineural Deafness

  • Sensorineural Hearing Loss Disorder

  • Hearing Loss, Sensorineural

  • Central Hearing Loss

  • High Frequency Deafness

  • High Frequency Hearing Loss

  • High-Frequency Hearing Loss

  • Perceptive Deafness

  • Perceptive Hearing Loss

  • Perceptive Hearing Loss Or Deafness

  • Hearing Loss Sensorineural

  • Deafness Sensorineural

  • Hearing Loss High-Frequency

  • Hearing Loss, Central

  • Hearing Loss, High-Frequency

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

生物種 Symbol 由来 ID
Mus musculus REST MGD MGI:104897
Rattus norvegicus REST RGD RGD:621069
Macaca mulatta REST VGNC VGNC:76898
Canis familiaris REST VGNC VGNC:45480
Others REST NCBI