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  2. EFNA5 - ephrin A5 Gene

EFNA5 - ephrin A5 Gene

中文名称:肾上腺素 A5

种属: Homo sapiens

同用名: AF1; EFL5; RAGS; EPLG7; GLC1M; LERK7

基因 ID: 1946 | 基因类型: protein coding

关于 EFNA5

Cytogenetic location: 5q21.3 Genomic coordinates (GRCh38): 5:107,376,894-107,670,937 (from NCBI)

This gene has 5 transcripts (splice variants), 289 orthologues and 7 paralogues. Ubiquitous expression in skin (RPKM 2.4), brain (RPKM 1.7) and 22 other tissues.

功能概要

Ephrin-A5 是 ephrin 基因家族的一员,可防止皮质神经元与星形胶质细胞共培养时的轴突捆绑,星形胶质细胞是晚期神经系统发育和分化的模型。 EPH 和 EPH 相关受体包含受体蛋白-酪氨酸激酶的最大亚家族,并且与介导发育事件有关,特别是在神经系统中。 EPH 受体通常有一个激酶结构域和一个含有富含半胱氨酸结构域和 2 个纤连蛋白 III 型重复序列的胞外区。肝配蛋白配体和受体已由 Eph 命名委员会 (1997) 命名。基于它们的结构和序列关系,肝配蛋白分为肝配蛋白-A (EFNA) 类和肝配蛋白 B (EFNB) 类,前者通过糖基磷脂酰肌醇键固定在膜上,后者是跨膜蛋白。基于其细胞外结构域序列的相似性和它们对结合肝配蛋白-A 和肝配蛋白-B 配体的亲和力,Eph 受体家族同样分为 2 组。[RefSeq 提供,2008 年 7 月]

Ephrin-A5, a member of the ephrin gene family, prevents axon bundling in cocultures of cortical neurons with astrocytes, a model of late stage nervous system development and differentiation. The EPH and EPH-related receptors comprise the largest subfamily of receptor protein-tyrosine kinases and have been implicated in mediating developmental events, particularly in the nervous system. Eph Receptors typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin ligands and receptors have been named by the Eph Nomenclature Committee (1997). Based on their structures and sequence relationships, Ephrins are divided into the ephrin-A (EFNA) class, which are anchored to the membrane by a glycosylphosphatidylinositol linkage, and the ephrin-B (EFNB) class, which are transmembrane proteins. The Eph family of receptors are similarly divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. [provided by RefSeq, Jul 2008]

EFNA5 基因产物(2)

mRNA Protein Name
NM_001410773.1 NP_001397702.1 ephrin-A5 isoform 2 precursor
NM_001962.3 NP_001953.1 ephrin-A5 isoform 1 precursor
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 ephrin receptor binding IPI
IPI: 通过物理相互作用推断
11519828 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
19836338 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
NOT involved in apoptotic process IDA
IDA: 通过直接分析推断
11870224 GOA
involved in ephrin receptor signaling pathway IDA
IDA: 通过直接分析推断
11870224 GOA
acts upstream of or within negative regulation of substrate adhesion-dependent cell spreading IDA
IDA: 通过直接分析推断
23242526 GOA
involved in regulation of GTPase activity IDA
IDA: 通过直接分析推断
11870224 GOA
involved in regulation of actin cytoskeleton organization IDA
IDA: 通过直接分析推断
11870224 GOA
acts upstream of or within regulation of cell morphogenesis IDA
IDA: 通过直接分析推断
23242526 GOA
involved in regulation of cell-cell adhesion IDA
IDA: 通过直接分析推断
11870224 GOA
involved in regulation of focal adhesion assembly IDA
IDA: 通过直接分析推断
11870224 GOA
involved in regulation of microtubule cytoskeleton organization IDA
IDA: 通过直接分析推断
11870224 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in external side of plasma membrane IDA
IDA: 通过直接分析推断
11870224 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

EFNA5 蛋白结构

Ephrin

Ephrin: Ephrin (27 - 163)

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

ephrin-A5

AL-1

重组 EFNA5 蛋白

目录号 产品名 蛋白编号 纯度
HY-P70379 Ephrin-A5/EFNA5 Protein, Human (HEK293, Fc) P52803 (Q21-N203) ≥95%
HY-P73012 Ephrin-A5/EFNA5 Protein, Human (HEK293, His) P52803 (Q21-N203) ≥95%

关联疾病

疾病名称 别名
Cortical Senile Cataract
Persistent Hyperplastic Primary Vitreous

Congenital Retinal Detachment

Ncrna Disease

Non-Syndromic Congenital Retinal Non-Attachment

Pfvs

Phpv

Persistent Fetal Vasculature Syndrome

Omenn Syndrome

Histiocytic Medullary Reticulosis

Severe Combined Immunodeficiency With Hypereosinophilia

Combined Immunodeficiency With Hypereosinophilia

Reticuloendotheliosis, Familial, With Eosinophilia

Reticuloendotheliosis Familial With Eosinophilia

Familial Reticuloendotheliosis

Omenn'S Syndrome

OS

Malignant Histiocytosis

Cataract

Cataracts

Cat - [Cataract]

Cataract Form

Lens Opacity

Lens Opacities

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 EFNA5 MGD MGI:107444
Felis catus EFNA5 VGNC VGNC:102192
Rattus norvegicus EFNA5 RGD RGD:620391
Bos taurus EFNA5 VGNC VGNC:28358
Macaca mulatta EFNA5 VGNC VGNC:72168
Canis familiaris EFNA5 VGNC VGNC:53168
Others EFNA5 NCBI