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  2. EIF4A3 - eukaryotic translation initiation factor 4A3 Gene

EIF4A3 - eukaryotic translation initiation factor 4A3 Gene

中文名称:真核翻译起始因子 4A3

种属: Homo sapiens

同用名: Fal1; RCPS; DDX48; MUK34; NUK34; NMP265; eIF4AIII; eIF4A-III; eIF-4A-III

基因 ID: 9775 | 基因类型: protein coding

关于 EIF4A3

Cytogenetic location: 17q25.3 Genomic coordinates (GRCh38): 17:80,134,369-80,147,128 (from NCBI)

This gene has 9 transcripts (splice variants), 230 orthologues, 38 paralogues and is associated with 3 phenotypes. Ubiquitous expression in bone marrow (RPKM 66.0), adrenal (RPKM 43.4) and 25 other tissues.

功能概要

该基因编码 DEAD box 蛋白家族的一个成员。以保守基序 Asp-Glu-Ala-Asp (DEAD) 为特征的 DEAD 盒蛋白是推定的 RNA 解旋酶。它们涉及许多涉及 RNA 二级结构改变的细胞过程,例如翻译起始、核和线粒体剪接以及核糖体和剪接体组装。根据它们的分布模式,该家族的一些成员被认为参与了胚胎发生、精子发生以及细胞生长和分裂。该基因编码的蛋白质是核基质蛋白。其氨基酸序列与翻译起始因子 eIF4AI 和 eIF4AII (DEAD 盒蛋白家族的另外两个成员) 的氨基酸序列高度相似。[RefSeq 提供,2008 年 7 月]

This gene encodes a member of the DEAD box protein family. DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure, such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. The protein encoded by this gene is a nuclear matrix protein. Its amino acid sequence is highly similar to the amino acid sequences of the translation initiation factors eIF4AI and eIF4AII, two Other members of the DEAD box protein family. [provided by RefSeq, Jul 2008]

EIF4A3 基因产物(2)

mRNA Protein Name
NM_001411099.1 NP_001398028.1 eukaryotic initiation factor 4A-III isoform 2
NM_014740.4 NP_055555.1 eukaryotic initiation factor 4A-III isoform 1
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 ATP binding IDA
IDA: 通过直接分析推断
10523622 GOA
enables RNA helicase activity IDA
IDA: 通过直接分析推断
10523622 GOA
enables mRNA binding IDA
IDA: 通过直接分析推断
22961380 GOA
enables poly(A) binding IDA
IDA: 通过直接分析推断
10523622 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
10523622 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of U2-type catalytic step 1 spliceosome IDA
IDA: 通过直接分析推断
29301961 GOA
part of catalytic step 2 spliceosome IDA
IDA: 通过直接分析推断
11991638 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
10523622 GOA
part of exon-exon junction complex IDA
IDA: 通过直接分析推断
16601204 GOA
part of exon-exon junction complex IPI
IPI: 通过物理相互作用推断
16931718 GOA
located in nucleus IDA
IDA: 通过直接分析推断
29301961 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

EIF4A3 蛋白结构

DEAD

DEAD: DEAD/DEAH box helicase (63 - 225)

Helicase_C

Helicase_C: Helicase conserved C-terminal domain (296 - 372)

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

eukaryotic initiation factor 4A-III

ATP-dependent RNA helicase DDX48

EIF4A3 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
种属内
EIF4A3 P38919 PAX4 Homo sapiens Q3KNR5 32296183
种属内
EIF4A3 P38919 PAX4 Homo sapiens Q3KNR5 32296183
种属内
EIF4A3 P38919 PAX4 Homo sapiens Q3KNR5 32296183
种属内
EIF4A3 P38919 CNKSR3 Homo sapiens Q6P9H4 32296183
种属内
EIF4A3 P38919 CNKSR3 Homo sapiens Q6P9H4 32296183
种属内
EIF4A3 P38919 CNKSR3 Homo sapiens Q6P9H4 32296183
种属内
EIF4A3 P38919 REL Homo sapiens Q04864-2 32296183
种属内
EIF4A3 P38919 REL Homo sapiens Q04864-2 32296183
种属内
EIF4A3 P38919 REL Homo sapiens Q04864-2 32296183
种属内
EIF4A3 P38919 CARD9 Homo sapiens Q9H257-2 32296183
种属内
EIF4A3 P38919 CARD9 Homo sapiens Q9H257-2 32296183
种属内
EIF4A3 P38919 CARD9 Homo sapiens Q9H257-2 32296183
种属内
EIF4A3 P38919 DISC1 Homo sapiens Q9NRI5-2 32296183
种属内
EIF4A3 P38919 DISC1 Homo sapiens Q9NRI5-2 32296183
种属内
EIF4A3 P38919 DISC1 Homo sapiens Q9NRI5-2 32296183
种属内
EIF4A3 P38919 VRTN Homo sapiens Q9H8Y1 32296183
种属内
EIF4A3 P38919 VRTN Homo sapiens Q9H8Y1 32296183
种属内
EIF4A3 P38919 VRTN Homo sapiens Q9H8Y1 32296183
种属内
EIF4A3 P38919 MEOX2 Homo sapiens Q6FHY5 32296183
种属内
EIF4A3 P38919 MEOX2 Homo sapiens Q6FHY5 32296183
种属内
EIF4A3 P38919 MEOX2 Homo sapiens Q6FHY5 32296183
种属内
EIF4A3 P38919 ZXDB Homo sapiens P98169 32296183
种属内
EIF4A3 P38919 ZXDB Homo sapiens P98169 32296183
种属内
EIF4A3 P38919 ZXDB Homo sapiens P98169 32296183
种属内
EIF4A3 P38919 NOM1 Homo sapiens Q5C9Z4 35271311
种属内
EIF4A3 P38919 MEOX1 Homo sapiens P50221 32296183
种属内
EIF4A3 P38919 MEOX1 Homo sapiens P50221 32296183
种属内
EIF4A3 P38919 MEOX1 Homo sapiens P50221 32296183
种属内
EIF4A3 P38919 CASC3 Homo sapiens O15234
TAP
16170325
种属内
EIF4A3 P38919 CASC3 Homo sapiens O15234 14973490
种属内
EIF4A3 P38919 CASC3 Homo sapiens O15234 16209946
种属内
EIF4A3 P38919 CASC3 Homo sapiens O15234 16601204
种属内
EIF4A3 P38919 MAGOH Homo sapiens P61326 23084401
种属内
EIF4A3 P38919 MAGOH Homo sapiens P61326 19478851
种属内
EIF4A3 P38919 MAGOH Homo sapiens P61326 14730019
种属内
EIF4A3 P38919 MAGOH Homo sapiens P61326 16601204
种属内
EIF4A3 P38919 MAGOH Homo sapiens P61326 23084401
种属内
EIF4A3 P38919 MAGOH Homo sapiens P61326
GMS
23084401
种属内
EIF4A3 P38919 MAGOH Homo sapiens P61326 23084401
种属内
EIF4A3 P38919 MAGOH Homo sapiens P61326
TAP
18066079
种属内
EIF4A3 P38919 MAGOH Homo sapiens P61326 19410547
种属内
EIF4A3 P38919 MAGOH Homo sapiens P61326 16209946
种属内
EIF4A3 P38919 POLR2G Homo sapiens P62487 32296183
种属内
EIF4A3 P38919 POLR2G Homo sapiens P62487 32296183
种属内
EIF4A3 P38919 POLR2G Homo sapiens P62487 32296183
种属内
EIF4A3 P38919 PRMT5 Homo sapiens O14744 32296183
种属内
EIF4A3 P38919 PRMT5 Homo sapiens O14744 32296183
种属内
EIF4A3 P38919 THRAP3 Homo sapiens Q9Y2W1 23084401
种属内
EIF4A3 P38919 PSMA1 Homo sapiens P25786 32296183
种属内
EIF4A3 P38919 PSMA1 Homo sapiens P25786 32296183
种属内
EIF4A3 P38919 DDX56 Homo sapiens Q9NY93 32296183
种属内
EIF4A3 P38919 DDX56 Homo sapiens Q9NY93 32296183
种属内
EIF4A3 P38919 DDX56 Homo sapiens Q9NY93 32296183
种属内
EIF4A3 P38919 UPF3B Homo sapiens Q9BZI7 19410547
种属内
EIF4A3 P38919 UPF3B Homo sapiens Q9BZI7 23084401
种属内
EIF4A3 P38919 UPF3B Homo sapiens Q9BZI7
GMS
23084401
种属内
EIF4A3 P38919 UPF3B Homo sapiens Q9BZI7 15361857
种属内
EIF4A3 P38919 UPF3B Homo sapiens Q9BZI7 23084401
种属内
EIF4A3 P38919 UPF3B Homo sapiens Q9BZI7 16601204
种属内
EIF4A3 P38919 UPF3B Homo sapiens Q9BZI7 16209946
种属内
EIF4A3 P38919 UPF3B Homo sapiens Q9BZI7 19478851
种属内
EIF4A3 P38919 CWC22 Homo sapiens Q9HCG8 23236153
种属内
EIF4A3 P38919 CWC22 Homo sapiens Q9HCG8 23084401
种属内
EIF4A3 P38919 CWC22 Homo sapiens Q9HCG8 23236153
种属内
EIF4A3 P38919 CWC22 Homo sapiens Q9HCG8 22365833
种属内
EIF4A3 P38919 CWC22 Homo sapiens Q9HCG8 29997244
种属内
EIF4A3 P38919 RBM8A Homo sapiens Q9Y5S9 23084401
种属内
EIF4A3 P38919 RBM8A Homo sapiens Q9Y5S9 23084401
种属内
EIF4A3 P38919 RBM8A Homo sapiens Q9Y5S9 16209946
种属内
EIF4A3 P38919 RBM8A Homo sapiens Q9Y5S9
GMS
23084401
种属内
EIF4A3 P38919 RBM8A Homo sapiens Q9Y5S9 23084401
种属内
EIF4A3 P38919 RBM8A Homo sapiens Q9Y5S9 19410547
种属内
EIF4A3 P38919 RBM8A Homo sapiens Q9Y5S9 16601204
种属内
EIF4A3 P38919 CDCA7L Homo sapiens Q96GN5 25416956
种属内
EIF4A3 P38919 CDCA7L Homo sapiens Q96GN5 25416956
种属内
EIF4A3 P38919 TRIM27 Homo sapiens P14373 32296183
种属内
EIF4A3 P38919 TRIM27 Homo sapiens P14373 32296183
种属内
EIF4A3 P38919 LNX1 Homo sapiens Q8TBB1 32296183
种属内
EIF4A3 P38919 LNX1 Homo sapiens Q8TBB1 32296183
种属内
EIF4A3 P38919 LNX1 Homo sapiens Q8TBB1 32296183
种属内
EIF4A3 P38919 NIF3L1 Homo sapiens Q9GZT8 32296183
种属内
EIF4A3 P38919 NIF3L1 Homo sapiens Q9GZT8 32296183
种属内
EIF4A3 P38919 NIF3L1 Homo sapiens Q9GZT8 32296183
种属内
EIF4A3 P38919 DDIT4L Homo sapiens Q96D03 32296183
种属内
EIF4A3 P38919 DDIT4L Homo sapiens Q96D03 32296183
种属内
EIF4A3 P38919 DDIT4L Homo sapiens Q96D03 32296183
种属内
EIF4A3 P38919 EHMT2 Homo sapiens Q96KQ7 32296183
种属内
EIF4A3 P38919 EHMT2 Homo sapiens Q96KQ7 32296183
种属内
EIF4A3 P38919 EHMT2 Homo sapiens Q96KQ7 32296183
种属内
EIF4A3 P38919 CCDC174 Homo sapiens Q6PII3 32296183
种属内
EIF4A3 P38919 CCDC174 Homo sapiens Q6PII3 35271311
种属内
EIF4A3 P38919 CCDC174 Homo sapiens Q6PII3 32296183
种属内
EIF4A3 P38919 CCDC174 Homo sapiens Q6PII3 16189514
种属内
EIF4A3 P38919 CCDC174 Homo sapiens Q6PII3 32296183
种属内
EIF4A3 P38919 DRG2 Homo sapiens P55039 32296183
种属内
EIF4A3 P38919 DRG2 Homo sapiens P55039 32296183
种属内
EIF4A3 P38919 DRG2 Homo sapiens P55039 32296183
种属内
EIF4A3 P38919 PICK1 Homo sapiens Q9NRD5 32296183
种属内
EIF4A3 P38919 PICK1 Homo sapiens Q9NRD5 32296183
种属内
EIF4A3 P38919 PICK1 Homo sapiens Q9NRD5 32296183
种属内
EIF4A3 P38919 PDCD4 Homo sapiens Q53EL6 32296183
种属内
EIF4A3 P38919 PDCD4 Homo sapiens Q53EL6 25416956
种属间: 跨种属相互作用 种属内: 同种属相互作用

EIF4A3 抗体

目录号 产品名 应用 反应物种
HY-P82077 eIF4A3 Antibody (YA1822) WB, IHC-P, ICC/IF, IP, FC Human, Mouse, Rat

关联疾病

疾病名称 别名
Robin Sequence With Cleft Mandible And Limb Anomalies

Richieri Costa Pereira Syndrome

Richieri Costa-Pereira Syndrome

Richieri-Costa-Pereira Syndrome

RCPS

Richieri-Costa And Pereira Form Of Acrofacial Dysostosis

Short Stature, Robin Sequence, Cleft Mandible, Pre/Postaxial Hand Anomalies, And Clubfoot

Short Stature-Pierre Robin Sequence-Cleft Mandible-Hand Anomalies Clubfoot Syndrome

Short Stature-Pierre Robin Syndrome-Cleft Mandible-Hand Anomalies Clubfoot Syndrome

Richieri-Costa And Pereira Syndrome

Mandibulofacial Dysostosis, Guion-Almeida Type

Mandibulofacial Dysostosis With Microcephaly

Mandibulofacial Dysostosis-Microcephaly Syndrome

MFDGA

MFDM

Mfdm Syndrome

Growth And Mental Retardation, Mandibulofacial Dysostosis, Microcephaly, And Cleft Palate

Growth Delay - Intellectual Disability - Mandibulofacial Dysostosis - Microcephaly - Cleft Palate

Growth Delay-Intellectual Disability-Mandibulofacial Dysostosis-Microcephaly-Cleft Palate Syndrome

Dysostosis, Mandibulofacial, Guion-Almeida Type

Acrofacial Dysostosis 1, Nager Type

Nager Syndrome

Nager Acrofacial Dysostosis

AFD1

Preaxial Acrofacial Dysostosis

Mandibulofacial Dysostosis, Treacher Collins Type, With Limb Anomalies

Afd, Nager Type

Nager Acrofacial Dysostosis Syndrome

Nafd

Acrofacial Dysostosis, Nager Type

Afd

Preaxial Manibulofacial Dysostosis

Split Hand Deformity-Mandibulofacial Dysostosis

Preaxial Mandibulofacial Dysostosis

Mandibulofacial Dysostosis With Preaxial Limb Anomalies

Preaxial Acrodysostosis

Afd Nager Type

Mandibulofacial Dysostosis Treacher Collins Type With Limb Anomalies

Acrofacial Dysostosis
Burn-Mckeown Syndrome

Choanal Atresia-Hearing Loss-Cardiac Defects-Craniofacial Dysmorphism Syndrome

Oculootofacial Dysplasia

BMKS

Oofd

Bilateral Choanal Atresia, Cardiac Defects, Deafness, And Dysmorphic Appearance

Choanal Atresia - Deafness - Cardiac Defects - Dysmorphism Syndrome

Choanal Atresia Deafness Cardiac Defects Dysmorphism

Oculo-Oto-Facial Dysplasia

Learning Disability

Learning Disabilities

Learning Disorders

Academic Skill Disorder

Learning Disorder

Thrombocytopenia-Absent Radius Syndrome

Tar Syndrome

Radial Aplasia-Thrombocytopenia Syndrome

Absent Radii And Thrombocytopenia

TAR

Chromosome 1q21.1 Deletion Syndrome, 200-Kb

Thrombocytopenia Absent Radius Syndrome

Thrombocytopenia Absent Radii

Chromosome 1q21.1 Deletion Syndrome

Thrombocytopenia With Absent Radii Syndrome

Radial Aplasia-Amegakaryocytic Thrombocytopenia

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
Mus musculus EIF4A3 MGD MGI:1923731
Macaca mulatta EIF4A3 VGNC VGNC:99146
Rattus norvegicus EIF4A3 RGD RGD:1591139
Bos taurus EIF4A3 VGNC VGNC:28406
Canis familiaris EIF4A3 VGNC VGNC:40281
Felis catus EIF4A3 VGNC VGNC:61789