1. Gene
  2. EIF2S3 - eukaryotic translation initiation factor 2 subunit gamma Gene

EIF2S3 - eukaryotic translation initiation factor 2 subunit gamma Gene

中文名称:真核翻译起始因子 2 亚基 γ

种属: Homo sapiens

同用名: EIF2; EIF2G; MEHMO; MRXSBRK; eIF-2gA; EIF2gamma

基因 ID: 1968 | 基因类型: protein coding

关于 EIF2S3

Cytogenetic location: Xp22.11 Genomic coordinates (GRCh38): X:24,054,956-24,078,810 (from NCBI)

This gene has 5 transcripts (splice variants), 158 orthologues, 18 paralogues and is associated with 3 phenotypes. Ubiquitous expression in ovary (RPKM 61.4), lymph node (RPKM 53.4) and 25 other tissues.

功能概要

由该基因编码的蛋白质是参与将甲硫氨酰-tRNA (i) 募集到 40 S 核糖体亚基的异源三聚体 GTP 结合蛋白的最大亚基。[RefSeq 提供,2010 年 1 月]

The protein encoded by this gene is the largest subunit of a heterotrimeric GTP-binding protein involved in the recruitment of methionyl-tRNA(i) to the 40 S ribosomal subunit. [provided by RefSeq, Jan 2010]

EIF2S3 基因产物(1)

mRNA Protein Name
NM_001415.4 NP_001406.1 eukaryotic translation initiation factor 2 subunit 3
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 protein binding IPI
IPI: 通过物理相互作用推断
16288713 GOA
enables translation factor activity, RNA binding IDA
IDA: 通过直接分析推断
10900014 GOA
enables translation initiation factor activity IDA
IDA: 通过直接分析推断
10900014 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cytoplasmic translational initiation IMP
IMP: 通过突变表型推断
31836389 GOA
involved in translational initiation IDA
IDA: 通过直接分析推断
10900014 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cytoplasm IDA
IDA: 通过直接分析推断
12426392 GOA
part of eukaryotic translation initiation factor 2 complex IDA
IDA: 通过直接分析推断
23063529 GOA
part of eukaryotic translation initiation factor 2 complex IPI
IPI: 通过物理相互作用推断
31836389 GOA
NOT located in nucleus IDA
IDA: 通过直接分析推断
12426392 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

EIF2S3 蛋白结构

GTP_EFTU

GTP_EFTU: Elongation factor Tu GTP binding domain (40 - 244)

GTP_EFTU_D2

GTP_EFTU_D2: Elongation factor Tu domain 2 (276 - 359)

eIF2_C

eIF2_C: Initiation factor eIF2 gamma, C terminal (368 - 459)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 472 a.a.
蛋白主名 其他名称

eukaryotic translation initiation factor 2 subunit 3

eIF-2-gamma X

EIF2S3 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
Intra EIF2S3 P41091 EIF2S1 Homo sapiens P05198
Anti Tag CoIP
35271311
Intra EIF2S3 P41091 EIF2S1 Homo sapiens P05198
ELISA
16288713
Intra EIF2S3 P41091 OTUD7B Homo sapiens Q6GQQ9-2
Y2H Array
32814053
Intra EIF2S3 P41091 OTUD7B Homo sapiens Q6GQQ9-2
Y2H Pooling
32814053
Intra EIF2S3 P41091 OTUD7B Homo sapiens Q6GQQ9-2
Validated Y2H
32814053
Intra EIF2S3 P41091 RASSF1 Homo sapiens Q9NS23-4
Validated Y2H
32814053
Intra EIF2S3 P41091 RASSF1 Homo sapiens Q9NS23-4
Y2H Array
32814053
Intra EIF2S3 P41091 HTT Homo sapiens P42858
Y2H Pooling
32814053
Intra EIF2S3 P41091 HTT Homo sapiens P42858
Validated Y2H
32814053
Intra EIF2S3 P41091 HTT Homo sapiens P42858
Y2H Array
32814053
Intra EIF2S3 P41091 MAP3K5 Homo sapiens Q99683
Validated Y2H
32814053
Intra EIF2S3 P41091 MAP3K5 Homo sapiens Q99683
Y2H Array
32814053
Intra EIF2S3 P41091 MAP3K5 Homo sapiens Q99683
Y2H Pooling
32814053
Intra EIF2S3 P41091 EIF2S2 Homo sapiens P20042
Anti Tag CoIP
35271311
Intra EIF2S3 P41091 EIF2S2 Homo sapiens P20042
ELISA
16288713
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Mehmo Syndrome

Mental Retardation, Epileptic Seizures, Hypogonadism And Hypogenitalism, Microcephaly, And Obesity

MEHMO

Mrxs20

Mrxs25

X-Linked Intellectual Disability-Epileptic Seizures-Hypogenitalism-Microcephaly-Obesity Syndrome

Mrxsbrk

Mental Retardation, X-Linked, Syndromic 20

Mental Retardation, X-Linked, Syndromic 25

Mental Retardation, X-Linked, Syndromic, Borck Type

Syndromic X-Linked Mental Retardation 20

Syndromic X-Linked Mental Retardation 25

Intellectual Disability, Epileptic Seizures, Hypogonadism And Hypogenitalism, Microcephaly, And Obesity

X-Linked Mehmo Syndrome

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

Hypopituitarism

Pituitary Hypofunction

Pituitary Insufficiency

Pituitary Hormone Deficiency

Subpituitarism

Hypophyseal Dystrophy

Hypohypophysism

Anterior Pituitary Insufficiency

Deficient Secretion Of One Or More Pituitary Hormones

Hypopituitarism Syndrome

Pituitary Deficiency

Pituitary Failure

Pituitary Insufficiency Nos

Anterior Pituitary Hypofunction

Deficient Secretion Of All Pituitary Hormones

Hypopituitary Dwarfism

Hyposomatotropic Dwarfism

Hypophyseal Dwarfism

Hypopituitary Cachexia

Hypophyseal Short Stature

Panhypopituitarism Syndrome

Pituitary Cachexia

Juvenile Hypopituitarism

Pituitary Dwarfism

Pituitary Gland Hypofunction

Primary Hypopituitarism

Secondary Hypogonadism

Prepubertal Panhypopituitarism

Prepubertal Dwarfism

Postpartum Panhypopituitary Syndrome

Postpartum Hypopituitarism

Pituitary Short Stature

Pituitary Infantilism

Pituitary Hypogonadism

Pituitary Hypoadrenocorticism

Microcephaly

Microencephaly

Microcephalus

Microcephalic

Nanocephaly

Congenital Microcephaly

Brain Hypoplasia

Brain Nondevelopment

Cephalic Hypoplasia

Undeveloped Cerebrum

Undeveloped Brain

Micrencephalon

Micrencephaly

Syndromic X-Linked Intellectual Disability

X-Linked Syndromic Intellectual Disability

Syndromic Intellectual Disability
Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder

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
Canis familiaris EIF2S3 VGNC VGNC:54137
Rattus norvegicus EIF2S3 RGD RGD:1561279
Mus musculus EIF2S3 MGD MGI:1349431