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  2. TDRD3 - tudor domain containing 3 Gene

TDRD3 - tudor domain containing 3 Gene

中文名称:含 Tudor 域 3

种属: Homo sapiens

基因 ID: 81550 | 基因类型: protein coding

关于 TDRD3

Cytogenetic location: 13q21.2 Genomic coordinates (GRCh38): 13:60,395,533-60,573,879 (from NCBI)

This gene has 9 transcripts (splice variants) and 211 orthologues. Ubiquitous expression in testis (RPKM 6.2), thyroid (RPKM 5.5) and 25 other tissues.

功能概要

启用染色质结合活性;甲基化组蛋白结合活性;和转录共激活因子活性。预测参与染色质组织和转录的正调控,DNA 模板化。位于高尔基体;胞质溶胶;和核质。与外显子-外显子连接复合体共定位。 [由基因组资源联盟提供,2022 年 4 月]

Enables chromatin binding activity; methylated histone binding activity; and transcription coactivator activity. Predicted to be involved in chromatin organization and positive regulation of transcription, DNA-templated. Located in Golgi apparatus; cytosol; and nucleoplasm. Colocalizes with exon-exon junction complex. [provided by Alliance of Genome Resources, Apr 2022]

TDRD3 基因产物(3)

mRNA Protein Name
NM_001146070.2 NP_001139542.1 tudor domain-containing protein 3 isoform 1
NM_001146071.1 NP_001139543.1 tudor domain-containing protein 3 isoform 2
NM_030794.2 NP_110421.1 tudor domain-containing protein 3 isoform 2
基因本体论
  • 分子功能
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables chromatin binding IDA
IDA: 通过直接分析推断
21172665 GOA
enables methylated histone binding IDA
IDA: 通过直接分析推断
21172665 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
23066109 GOA
enables transcription coactivator activity IDA
IDA: 通过直接分析推断
21172665 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of DNA topoisomerase III-beta-TDRD3 complex IPI
IPI: 通过物理相互作用推断
28176834 GOA
part of exon-exon junction complex IDA
IDA: 通过直接分析推断
20930030 GOA
located in nucleus IDA
IDA: 通过直接分析推断
21172665 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

TDRD3 蛋白结构

UBA

UBA: UBA/TS-N domain (194 - 230)

TUDOR

TUDOR: Tudor domain (553 - 611)

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  • 651 a.a.
蛋白主名 其他名称

tudor domain-containing protein 3

TDRD3 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 TDRD3 Q9H7E2 POLR2A Homo sapiens P24928
Fluorescence Spectr
23066109
Intra TDRD3 Q9H7E2 POLR2A Homo sapiens P24928
NMR
23066109
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
Fragile X Syndrome

FXS

Martin-Bell Syndrome

Fraxa Syndrome

Marker X Syndrome

X-Linked Mental Retardation And Macroorchidism

Fragile X Mental Retardation Syndrome

Fra Syndrome

Mental Retardation, X-Linked, Associated With Marxq28

X-Linked Intellectual Disability And Macroorchidism

Frax Syndrome

Symptomatic Form Of Fragile X Syndrome In Female Carriers

Fragile-X Syndrome

Fraxe Syndrome

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 TDRD3 VGNC VGNC:97224
Rattus norvegicus TDRD3 RGD RGD:1310126
Bos taurus TDRD3 VGNC VGNC:35718
Mus musculus TDRD3 MGD MGI:2444023
Macaca mulatta TDRD3 VGNC VGNC:79258
Felis catus TDRD3 VGNC VGNC:66047