1. Gene
  2. YWHAE - tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon Gene

YWHAE - tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon Gene

中文名称:酪氨酸 3-单加氧酶/色氨酸 5-单加氧酶激活蛋白 epsilon

种属: Homo sapiens

同用名: MDS; HEL2; MDCR; KCIP-1; 14-3-3E

基因 ID: 7531 | 基因类型: protein coding

关于 YWHAE

Cytogenetic location: 17p13.3 Genomic coordinates (GRCh38): 17:1,344,275-1,400,222 (from NCBI)

This gene has 13 transcripts (splice variants), 1 gene allele, 217 orthologues, 6 paralogues and is associated with 72 phenotypes. Ubiquitous expression in brain (RPKM 317.4), kidney (RPKM 169.5) and 25 other tissues.

功能概要

该基因产物属于 14-3-3 蛋白家族,通过与含磷酸丝氨酸的蛋白结合来介导信号转导。这种高度保守的蛋白质家族存在于植物和哺乳动物中,并且这种蛋白质与小鼠直系同源物 100% 相同。它与 CDC25 磷酸酶、RAF1 和 IRS1 蛋白相互作用,表明它在与信号转导相关的多种生化活动中发挥作用,例如细胞分裂和胰岛素敏感性调节。它还与小细胞肺癌的发病机制有关。已发现该基因的两种转录变体,一种是蛋白质编码,另一种是非蛋白质编码。[RefSeq 提供,2008 年 8 月]

This gene product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins. This highly conserved protein family is found in both Plants and mammals, and this protein is 100% identical to the mouse ortholog. It interacts with CDC25 phosphatases, RAF1 and IRS1 proteins, suggesting its role in diverse biochemical activities related to signal transduction, such as cell division and regulation of Insulin sensitivity. It has also been implicated in the pathogenesis of small cell lung Cancer. Two transcript variants, one protein-coding and the other non-protein-coding, have been found for this gene. [provided by RefSeq, Aug 2008]

YWHAE 基因产物(1)

mRNA Protein Name
NM_006761.5 NP_006752.1 2014/3/3 protein epsilon
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 calcium channel inhibitor activity IDA
IDA: 通过直接分析推断
18029012 GOA
enables calcium channel regulator activity IDA
IDA: 通过直接分析推断
18029012 GOA
enables enzyme binding IPI
IPI: 通过物理相互作用推断
10788521 GOA
enables histone deacetylase binding IPI
IPI: 通过物理相互作用推断
10869435 GOA
enables identical protein binding IPI
IPI: 通过物理相互作用推断
17085597 GOA
enables phosphoprotein binding IPI
IPI: 通过物理相互作用推断
10869435 GOA
enables phosphoserine residue binding IPI
IPI: 通过物理相互作用推断
10869435 GOA
enables potassium channel regulator activity IDA
IDA: 通过直接分析推断
11953308 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
1266503 GOA
enables protein heterodimerization activity IPI
IPI: 通过物理相互作用推断
11953308 GOA
enables protein sequestering activity IDA
IDA: 通过直接分析推断
11118213 GOA
enables scaffold protein binding IPI
IPI: 通过物理相互作用推断
10409742 GOA
enables signaling adaptor activity IDA
IDA: 通过直接分析推断
22607805 GOA
enables transmembrane transporter binding IPI
IPI: 通过物理相互作用推断
11953308 GOA
enables ubiquitin protein ligase binding IPI
IPI: 通过物理相互作用推断
19725078 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
is active in cytoplasm IDA
IDA: 通过直接分析推断
11118213 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
12917326 GOA
located in cytosol IDA
IDA: 通过直接分析推断
31906564 GOA
is active in endoplasmic reticulum IDA
IDA: 通过直接分析推断
35343654 GOA
located in nucleus IDA
IDA: 通过直接分析推断
12917326 GOA
colocalizes with plasma membrane IDA
IDA: 通过直接分析推断
18029012 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

YWHAE 蛋白结构

14-3-3

14-3-3: 14-3-3 protein (4 - 237)

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

14-3-3 protein epsilon

14-3-3 epsilon

重组 YWHAE 蛋白

目录号 产品名 蛋白编号 纯度
HY-P7445 14-3-3 epsilon Protein, Human (GST) P62258/NP_006752.1 (M1-Q255) ≥95%

关联疾病

疾病名称 别名
Endometrial Stromal Sarcoma

Ess

Endometrial Stromal Sarcoma, High Grade

Undifferentiated Endometrial Sarcoma

Stromal Sarcoma Of The Corpus Uteri

Sarcoma Endometrial Stromal

Sarcoma, Endometrial Stromal

Undifferentiated Stromal Sarcoma

Kidney Clear Cell Sarcoma

Clear Cell Sarcoma Of Kidney

Childhood Kidney Clear Cell Sarcoma

Renal Clear Cell Sarcoma

Ccsk

Clear Cell Sarcoma Of The Kidney

Distal 17p13.3 Microdeletion Syndrome

Distal Del(17)(P13.3 )

Distal Monosomy 17p13.3

Miller-Dieker Lissencephaly Syndrome

Miller-Dieker Syndrome

Mds

MDLS

Miller Dieker Syndrome

Classical Lissencephaly Syndrome

Lissencephaly Due To 17p13.3 Deletion

Monosomy 17p13.3

Telomeric Deletion 17p

Classical Lissencephaly

Chromosome 17p13.3, Centromeric, Duplication Syndrome

Chromosome 17p13.3 Duplication Syndrome

17p13.3 Duplication Syndrome

17p13.3 Microduplication Syndrome

Trisomy 17p13.3

Chromosome 17p13.3 Centromeric Duplication Syndrome

Dup(17)(P13.3)

Endometrial Stromal Tumor

Endometrial Stromal Neoplasm

Endometrial Stromal Tumors

Endometrial Stromal Nodule
Lissencephaly

Pachygyria

Broad Gyri Of Cerebrum

Large Gyri Of Cerebrum

Macrogyria

Kidney Sarcoma

Renal Sarcoma

Sarcoma Of Kidney

Vaginal Endometrial Stromal Sarcoma
Vagina Sarcoma

Sarcoma Of The Vagina

Vaginal Sarcoma

Myxoid Leiomyosarcoma

Leiomyosarcoma, Myxoid

Lissencephaly 4

LIS4

Lissencephaly 4 With Microcephaly

Microlissencephaly

Lissencephaly, Type 4

Cellular Congenital Mesoblastic Nephroma
Adenosarcoma

Mullerian Adenosarcoma

Clear Cell Sarcoma

Sarcoma, Clear Cell

Adult Soft Part Clear Cell Sarcoma

Clear Cell Sarcoma Of Soft Parts

Malignant Melanoma Of Soft Parts

Malignant Melanoma Of Soft Tissues

Melanoma, Malignant, Of Soft Parts

Sarcoma Clear Cell

Congenital Mesoblastic Nephroma

Mesoblastic Nephroma

Nephroma, Mesoblastic

Lissencephaly 1

LIS1

Classic Lissencephaly

Ils

Subcortical Laminar Heterotopia

Lissencephaly Due To Lis1 Mutation

Lissencephaly Sequence, Isolated

Lissencephaly, Classic

Pafah1b1-Related Lissencephaly

Classical Lissencephaly

Lissencephaly Type 1

Lissencephaly-1

Subcortical Band Heterotopia

Double Cortex

Lissencephaly Classic

Lissencephaly Sequence Isolated

Isolated Lissencephaly Sequence

Type 1 Lissencephaly

Lissencephaly Syndrome Type 1

SBH

Sclh

Lissencephaly, Type 1

Type I Lissencephaly

Sudden Infant Death Syndrome

SIDS

Sudden Infant Death Syndrome, Susceptibility To

Cot Death

Crib Death

Sudden Death Of Nonspecific Cause In Infancy

Sudden Infant Death

Death, Sudden, Syndrome, Infant

Potocki-Lupski Syndrome

PTLS

Chromosome 17p11.2 Duplication Syndrome

17p11.2 Microduplication Syndrome

Duplication 17p11.2 Syndrome

Trisomy 17p11.2

Potocki-Lupski Syndrome (Dup(17)(P11.2p11.2))

17p11.2 Duplication Syndrome

Dup(17)(P11.2p11.2)

Pls

Chromosome 17, Trisomy 17p11 2

Lung Cancer

Lung Carcinoma

Non-Small Cell Lung Carcinoma

Lung Cancer, Susceptibility To

Lung Cancer, Protection Against

Adenocarcinoma Of Lung, Somatic

Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer

Lung Neoplasm

Carcinoma Of Lung

Lung Non-Small Cell Carcinoma

Non-Small Cell Lung Cancer

Nsclc

Lung Neoplasms

Malignant Neoplasm Of Lung

Alveolar Cell Carcinoma

Nonsmall Cell Lung Cancer, Somatic

Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer, Susceptibility To

Lung Cancer, Somatic

Lung Cancer, Resistance To

Cancer Of Lung

Cancer Of Bronchus

Cancer Of The Lung

Lung Malignancies

Lung Malignant Tumors

Malignant Lung Tumor

Malignant Tumor Of Lung

Pulmonary Cancer

Pulmonary Carcinoma

Pulmonary Neoplasms

Respiratory Carcinoma

LNCR

Adenocarcinoma Of Lung

Neoplasm Of Lung

Cancer Lung

Carcinoma Non-Small Cell Lung

Carcinoma, Non-Small-Cell Lung

Lung Cancers

Lung Carcinomas

Cancer, Lung

Cancer, Lung, Non-Small Cell

Primary Malignant Neoplasm Of Lung

Bronchioloalveolar Adenocarcinoma

Kidney Fibrosarcoma

Fibrosarcoma Of The Kidney

Polymicrogyria, Bilateral Perisylvian, X-Linked

Bilateral Perisylvian Polymicrogyria

Polymicrogyria, Bilateral Perisylvian

Pmgx

Perisylvian Syndrome, Congenital Bilateral

Cbps

Congenital Bilateral Perisylvian Syndrome

Perisylvian Syndrome

BPPX

Bpp

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

Schizophrenia

SCZD

Schizophrenia With Or Without An Affective Disorder

Schizophrenia 12

Schizophrenia, Susceptibility To

Schizophrenia-1

Dementia Praecox

Schizophrenia 1

Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder

Left Ventricular Noncompaction

Noncompaction Cardiomyopathy

Left Ventricular Hypertrabeculation

Lvnc

Spongy Myocardium

Isolated Noncompaction Of The Ventricular Myocardium

Left Ventricular Myocardial Noncompaction Cardiomyopathy

Fetal Myocardium

Honeycomb Myocardium

Hypertrabeculation Syndrome

Left Ventricular Non-Compaction

Lvht

Non-Compaction Of The Left Ventricular Myocardium

Ventricular Noncompaction, Left

Non-Compaction Cardiomyopathy

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
Bos taurus YWHAE VGNC VGNC:37045
Rattus norvegicus YWHAE RGD RGD:62000
Macaca mulatta YWHAE VGNC VGNC:104677
Mus musculus YWHAE MGD MGI:894689
Others YWHAE NCBI