1. Gene
  2. HECTD4 - HECT domain E3 ubiquitin protein ligase 4 Gene

HECTD4 - HECT domain E3 ubiquitin protein ligase 4 Gene

中文名称:HECT 结构域 E3 泛素蛋白连接酶 4

种属: Homo sapiens

同用名: HEEL; POTAGE; C12ord51; C12orf51

基因 ID: 283450 | 基因类型: protein coding

关于 HECTD4

This gene has 16 transcripts (splice variants), 205 orthologues and 24 paralogues. Ubiquitous expression in brain (RPKM 8.7), bone marrow (RPKM 7.2) and 25 other tissues.

功能概要

预计会启用泛素蛋白转移酶活性。参与葡萄糖稳态和葡萄糖代谢过程。预计是膜的组成部分。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to enable ubiquitin-protein transferase activity. Involved in glucose homeostasis and glucose metabolic process. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

HECTD4 基因产物(2)

mRNA Protein Name
NM_001109662.4 NP_001103132.4 probable E3 ubiquitin-protein ligase HECTD4 isoform 1
NM_001388303.1 NP_001375232.1 probable E3 ubiquitin-protein ligase HECTD4 isoform 2
基因本体论
  • 分子功能
  • 生物过程
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
15161933 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in glucose homeostasis IMP
IMP: 通过突变表型推断
23575436 GOA
involved in glucose metabolic process IMP
IMP: 通过突变表型推断
23575436 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

HECTD4 蛋白结构

HECT

HECT: HECT-domain (ubiquitin-transferase) (3934 - 4266)

  • 0
  • 700
  • 1400
  • 2100
  • 2800
  • 3500
  • 4272 a.a.
蛋白主名 其他名称

probable E3 ubiquitin-protein ligase HECTD4

AF-1 specific protein phosphatase

HECTD4 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
HECTD4 Q9Y4D8 YWHAZ Homo sapiens P63104 15161933
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
Bone Angioendothelial Sarcoma

Osseous Hemangiosarcoma

Bone Angiosarcoma

Noonan Syndrome 1

Noonan Syndrome

NS1

Male Turner Syndrome

Female Pseudo-Turner Syndrome

Turner Phenotype With Normal Karyotype

Noonan Syndrome With Pigmented Villonodular Synovitis

Turner'S Phenotype, Karyotype Normal

Familial Turner Syndrome

Noonan'S Syndrome

Noonan-Ehmke Syndrome

Ns

Pseudo-Ullrich-Turner Syndrome

Turner Syndrome In Female With X Chromosome

Turner-Like Syndrome

Ullrich-Noonan Syndrome

Noonan-Like/Multiple Giant Cell Lesion Syndrome

Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions

Pterygium Colli Syndrome

Noonan Syndrome, Type 1

Turner Syndrome, Male

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
Felis catus HECTD4 VGNC VGNC:62785
Rattus norvegicus HECTD4 RGD RGD:1309762
Bos taurus HECTD4 VGNC VGNC:106766
Canis familiaris HECTD4 VGNC VGNC:41644
Macaca mulatta HECTD4 VGNC VGNC:73245
Mus musculus HECTD4 MGD MGI:3647820