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  2. ATF4 - activating transcription factor 4 Gene

ATF4 - activating transcription factor 4 Gene

中文名称:激活转录因子 4

种属: Homo sapiens

同用名: CREB2; TXREB; CREB-2; TAXREB67

基因 ID: 468 | 基因类型: protein coding

关于 ATF4

Cytogenetic location: 22q13.1 Genomic coordinates (GRCh38): 22:39,520,559-39,522,686 (from NCBI)

This gene has 11 transcripts (splice variants), 269 orthologues and 1 paralogue. Ubiquitous expression in bone marrow (RPKM 183.9), fat (RPKM 87.6) and 25 other tissues.

功能概要

该基因编码的转录因子最初被鉴定为广泛表达的哺乳动物 DNA 结合蛋白,可结合 HTLV-1 LTR 中的税反应增强子元件。编码的蛋白质也被分离并表征为 cAMP 反应元件结合蛋白 2 (CREB-2) 。该基因编码的蛋白质属于 DNA 结合蛋白家族,包括 AP-1 转录因子家族、cAMP 反应元件结合蛋白 (CREB) 和 CREB 样蛋白。这些转录因子共享一个参与蛋白质-蛋白质相互作用的亮氨酸拉链区域,该区域位于一段碱性氨基酸的 C 端,充当 DNA 结合域。已经描述了编码相同蛋白质的两种替代转录物。两个假基因位于 X 染色体 q28 的一个区域,该区域包含一个大的倒置重复。[RefSeq 提供,2011 年 9 月]

This gene encodes a transcription factor that was originally identified as a widely expressed mammalian DNA binding protein that could bind a tax-responsive enhancer element in the LTR of HTLV-1. The encoded protein was also isolated and characterized as the cAMP-response element binding protein 2 (CREB-2). The protein encoded by this gene belongs to a family of DNA-binding proteins that includes the AP-1 family of transcription factors, cAMP-response element binding proteins (CREBs) and CREB-like proteins. These transcription factors share a leucine zipper region that is involved in protein-protein interactions, located C-terminal to a stretch of basic Amino acids that functions as a DNA binding domain. Two alternative transcripts encoding the same protein have been described. Two pseudogenes are located on the X chromosome at q28 in a region containing a large inverted duplication. [provided by RefSeq, Sep 2011]

ATF4 基因产物(2)

mRNA Protein Name
NM_001675.4 NP_001666.2 cyclic AMP-dependent transcription factor ATF-4
NM_182810.3 NP_877962.1 cyclic AMP-dependent transcription factor ATF-4
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables DNA binding IDA
IDA: 通过直接分析推断
15788408 GOA
enables DNA-binding transcription factor activity IDA
IDA: 通过直接分析推断
11960987 GOA
enables DNA-binding transcription factor activity, RNA polymerase II-specific IDA
IDA: 通过直接分析推断
11478948 GOA
enables RNA polymerase II-specific DNA-binding transcription factor binding IPI
IPI: 通过物理相互作用推断
11478948 GOA
enables identical protein binding IPI
IPI: 通过物理相互作用推断
16343488 GOA
enables leucine zipper domain binding IDA
IDA: 通过直接分析推断
11478948 GOA
enables promoter-specific chromatin binding IDA
IDA: 通过直接分析推断
17267404 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
9488481 GOA
enables protein kinase binding IPI
IPI: 通过物理相互作用推断
20873783 GOA
enables sequence-specific DNA binding IDA
IDA: 通过直接分析推断
22915762 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: 通过直接分析推断
28473536 GOA
contributes to transcription cis-regulatory region binding IDA
IDA: 通过直接分析推断
12871976 GOA
enables transcription cis-regulatory region binding IDA
IDA: 通过直接分析推断
21113145 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in HRI-mediated signaling IDA
IDA: 通过直接分析推断
32132706 GOA
involved in L-asparagine metabolic process IDA
IDA: 通过直接分析推断
11960987 GOA
involved in cellular response to glucose starvation IMP
IMP: 通过突变表型推断
22915762 GOA
involved in cellular response to leucine starvation IDA
IDA: 通过直接分析推断
17267404 GOA
involved in cellular response to oxidative stress IMP
IMP: 通过突变表型推断
21113145 GOA
involved in integrated stress response signaling IDA
IDA: 通过直接分析推断
32132707 GOA
involved in negative regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway IGI
IGI: 通过遗传相互作用推断
23392669 GOA
involved in positive regulation of DNA-templated transcription IDA
IDA: 通过直接分析推断
15775988 GOA
involved in positive regulation of DNA-templated transcription IMP
IMP: 通过突变表型推断
11960987 GOA
involved in positive regulation of gene expression IMP
IMP: 通过突变表型推断
16445384 GOA
involved in positive regulation of transcription by RNA polymerase I IMP
IMP: 通过突变表型推断
22915762 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: 通过直接分析推断
11478948 GOA
involved in positive regulation of transcription by RNA polymerase II IMP
IMP: 通过突变表型推断
15788408 GOA
involved in positive regulation of vascular endothelial growth factor production IMP
IMP: 通过突变表型推断
22915762 GOA
involved in regulation of osteoblast differentiation IDA
IDA: 通过直接分析推断
15109498 GOA
involved in response to endoplasmic reticulum stress IDA
IDA: 通过直接分析推断
12871976 GOA
involved in response to endoplasmic reticulum stress IMP
IMP: 通过突变表型推断
21113145 GOA
involved in response to nutrient levels IDA
IDA: 通过直接分析推断
11960987 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of ATF1-ATF4 transcription factor complex IDA
IDA: 通过直接分析推断
12871976 GOA
part of ATF4-CREB1 transcription factor complex IDA
IDA: 通过直接分析推断
12871976 GOA
part of CHOP-ATF4 complex IDA
IDA: 通过直接分析推断
11478948 GOA
part of CHOP-ATF4 complex IPI
IPI: 通过物理相互作用推断
18940792 GOA
located in Lewy body core IDA
IDA: 通过直接分析推断
23392669 GOA
part of RNA polymerase II transcription regulator complex IPI
IPI: 通过物理相互作用推断
20102225 GOA
colocalizes with centrosome IDA
IDA: 通过直接分析推断
20873783 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
23392669 GOA
located in neuron projection IDA
IDA: 通过直接分析推断
23392669 GOA
located in nuclear periphery IDA
IDA: 通过直接分析推断
23392669 GOA
located in nucleus IDA
IDA: 通过直接分析推断
11478948 GOA
part of protein-containing complex IDA
IDA: 通过直接分析推断
20873783 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

ATF4 蛋白结构

bZIP_1

bZIP_1: bZIP transcription factor (276 - 337)

  • 0
  • 100
  • 200
  • 300
  • 351 a.a.
蛋白主名 其他名称

cyclic AMP-dependent transcription factor ATF-4

DNA-binding protein TAXREB67

关联疾病

疾病名称 别名
Coffin-Lowry Syndrome

CLS

Coffin Syndrome 1

Coffin Syndrome

Intellectual Disability With Osteocartilaginous Abnormalities

Dwarfism, Lean Spastic Type

Lean Spastic Dwarfism

Mental Retardation With Osteocartilaginous Abnormalities

Coffin Lowry Syndrome

Fatty Liver Disease

Alcoholic Fatty Liver

Fatty Liver

Fatty Liver, Alcoholic

Fatty Change Of Liver

Hepatic Lipidosis

Steatosis Of Liver

Fatty Liver Alcoholic

Steatohepatitis

Etoh Fatty Liver

Etoh Fatty Liver Metamorphosis

Fatty Etoh Liver Necrosis

Liver Disease

Liver Failure

Liver Diseases

Abnormality Of The Liver

Liver Dysfunction

Disorder Of Liver

Hepatic Disorder

Hepatic Disease

Disease Of Bilirubin Metabolism

Disorder Of Bilirubin Metabolism

Liver Decompensation

Liver Function Failure

Hepatic Failure Nos

Liver Failure Nos

End Stage Liver Disease

Decompensated Liver Failure

Decompensation Of Liver Function

Hepatic Decompensation

Hepatic Insufficiency

Liver Cell Necrosis With Hepatic Failure

Liver Insufficiency

Decompensated Liver Disease

End Stage Liver Failure

Liver Necrosis With Hepatic Failure

Epiphyseal Dysplasia, Multiple, With Early-Onset Diabetes Mellitus

Wolcott-Rallison Syndrome

Med-Iddm Syndrome

Iddm-Med Syndrome

Wolcott Rallison Syndrome

WRS

Epiphyseal Dysplasia Multiple With Early-Onset Diabetes Mellitus

Early-Onset Diabetes Mellitus With Multiple Epiphyseal Dysplasia

Multiple Epiphyseal Dysplasia With Early-Onset Diabetes Mellitus

Leukodystrophy

Leukodystrophies

T-Cell Acute Lymphoblastic Leukemia

T-Cell Leukemia

Acute T Cell Leukemia

Precursor T Lymphoblastic Leukemia

Precursor T-Lymphoblastic Lymphoma/Leukemia

T Acute Lymphoblastic Leukemia

T-Cell Acute Lymphocytic Leukaemia

T-Cell Lymphoblastic Leukemia/Lymphoma

Leukemia T-Cell

Leukemia, T-Cell

Leukemia, Acute, Lymphoblastic, T-Cell

Leukemia, T-Cell Acute Lymphoblastic

Leukemia, Acute T-Cell

Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

Precursor T-Cell Lymphoblastic Lymphoma

Precursor T Cell Lymphoblastic Leukemia/Lymphoblastic Lymphoma

Leukoencephalopathy With Vanishing White Matter

Cree Leukoencephalopathy

Vanishing White Matter Disease

Ovarioleukodystrophy

Vanishing White Matter Leukodystrophy

Childhood Ataxia With Central Nervous System Hypomyelinization

Cach

Cach Syndrome

Myelinosis Centralis Diffusa

VWM

Cle

Childhood Ataxia With Central Nervous System Hypomyelination

Childhood Ataxia With Diffuse Central Nervous System Hypomyelination

Cach/Vwm

Cach/Vwm Syndrome

Childhood Ataxia With Central Nervous System Hypomyelination/Vanishing White Matter

Cree Leukoencehalopathy

Late Infantile Cach Syndrome

Juvenile Or Adult Cach Syndrome

Congenital Or Early Infantile Cach Syndrome

Leukodystrophy With Vanishing White Matter

Pancreatic Cancer

Pancreatic Carcinoma

Carcinoma Of Pancreas

Familial Pancreatic Carcinoma

Pancreatic Neoplasm

Pancreatic Carcinoma, Familial

Malignant Neoplasm Of Pancreas

Pancreatic Acinar Carcinoma

Pancreatic Tumor

Familial Pancreatic Cancer

Neoplasm Of The Pancreas

Cancer Of The Pancreas

Pancreatic Carcinoma, Somatic

Pancreatic Cancer, Somatic

Ca Body Of Pancreas

Ca Head Of Pancreas

Ca Tail Of Pancreas

Malignant Neoplasm Of Body Of Pancreas

Malignant Neoplasm Of Head Of Pancreas

Malignant Neoplasm Of Tail Of Pancreas

Pancreas Neoplasm

Exocrine Cancer

Exocrine Pancreas Carcinoma

Hereditary Pancreatic Cancer

Hereditary Pancreatic Carcinoma

PNCA

Pancreatic Cancer, Susceptibility To

Carcinoma Of Head Of Pancreas

Pancreatic Neoplasms

Pancreatic Tumors

Cancer, Pancreatic

Cancer Of Pancreas

Mixed Islet Cell With Exocrine Carcinoma Of Unspecified Site

Basal Cell Carcinoma

Basal Cell Cancer

Basal Cell Neoplasm

Basal Cell Carcinoma Of Skin

Malignant Basal Cell Tumor

Basal Cell Tumor

Epithelioma Basal Cell

Malignant Basal Cell Neoplasm

Rodent Ulcer

Carcinoma Basal Cell

Neoplasms, Basal Cell

Basal Cell Carcinomas

Experimental Organism Basal Cell Carcinoma

Nodulo-Ulcerative Basal Cell Carcinoma

Basalioma

Basal Cell Epithelioma Of Skin

Bcc - [Basal Cell Carcinoma] Of Skin

Rodent Ulcer Of Skin

Rodent Ulcer Of Unspecified Site

Basal Cell Epithelioma Of Unspecified Site

Retinitis Pigmentosa

RP

Rod-Cone Dystrophy

Autosomal Recessive Retinitis Pigmentosa

Non-Syndromic Retinitis Pigmentosa

Pericentral Pigmentary Retinopathy

Pigmentary Retinopathy

Tapetoretinal Degeneration

Rcd

Retinitis Pigmentosa Autosomal Recessive

ARRP

Retinitis Pigmentosa, Autosomal Recessive

Retinitis Pigmentosa 1

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus ATF4 RGD RGD:621863
Mus musculus ATF4 MGD MGI:88096
Canis familiaris ATF4 VGNC VGNC:38210
Bos taurus ATF4 VGNC VGNC:26242
Macaca mulatta ATF4 VGNC VGNC:107770
Felis catus ATF4 VGNC VGNC:68509