1. Gene
  2. TRIM38 - tripartite motif containing 38 Gene

TRIM38 - tripartite motif containing 38 Gene

中文名称:含三方基序 38

种属: Homo sapiens

同用名: RNF15; RORET

基因 ID: 10475 | 基因类型: protein coding

关于 TRIM38

This gene has 1 transcript (splice variant), 103 orthologues and 80 paralogues. Ubiquitous expression in spleen (RPKM 9.0), lymph node (RPKM 8.4) and 24 other tissues.

功能概要

该基因编码三联基序 (TRIM) 家族的成员。编码的蛋白包含一个 RING 型锌指、B 盒型锌指和 SPRY 结构域。这种蛋白质的功能尚未确定。该基因的假基因位于 4 号染色体的长臂上。[RefSeq 提供,2012 年 7 月]

This gene encodes a member of the tripartite motif (TRIM) family. The encoded protein contains a RING-type zinc finger, B box-type zinc finger and SPRY domain. The function of this protein has not been identified. A pseudogene of this gene is located on the long arm of chromosome 4. [provided by RefSeq, Jul 2012]

TRIM38 基因产物(1)

mRNA Protein Name
NM_006355.5 NP_006346.1 E3 ubiquitin-protein ligase TRIM38
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
23275563 GOA
enables transcription coactivator activity IDA
IDA: 通过直接分析推断
23077300 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

TRIM38 蛋白结构

zf-C3HC4_4

zf-C3HC4_4: zinc finger of C3HC4-type, RING (16 - 62)

zf-B_box

zf-B_box: B-box zinc finger (89 - 127)

PRY

PRY: SPRY-associated domain (294 - 342)

SPRY

SPRY: SPRY domain (344 - 452)

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

E3 ubiquitin-protein ligase TRIM38

RING-type E3 ubiquitin transferase TRIM38

TRIM38 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
TRIM38 O00635 FLJ13057 Homo sapiens Q53SE7 25416956
种属内
TRIM38 O00635 UBE2I Homo sapiens Q7KZS0 32296183
种属内
TRIM38 O00635 UBE2I Homo sapiens Q7KZS0 25416956
种属内
TRIM38 O00635 UBE2I Homo sapiens Q7KZS0 32296183
种属内
TRIM38 O00635 UBE2I Homo sapiens Q7KZS0 25416956
种属内
TRIM38 O00635 UBE2I Homo sapiens Q7KZS0 32296183
种属内
TRIM38 O00635 GC20 Homo sapiens Q6FG85 25416956
种属内
TRIM38 O00635 GC20 Homo sapiens Q6FG85 25416956
种属内
TRIM38 O00635 GC20 Homo sapiens Q6FG85 25416956
种属内
TRIM38 O00635 MTURN Homo sapiens Q8N3F0 32296183
种属内
TRIM38 O00635 RNF4 Homo sapiens P78317 32296183
种属内
TRIM38 O00635 RNF4 Homo sapiens P78317 32296183
种属内
TRIM38 O00635 RNF4 Homo sapiens P78317 32296183
种属内
TRIM38 O00635 TSPYL4 Homo sapiens Q9UJ04 32296183
种属内
TRIM38 O00635 HSPA8 Homo sapiens P11142 32296183
种属内
TRIM38 O00635 HSPA8 Homo sapiens P11142 25416956
种属内
TRIM38 O00635 HSPA1L Homo sapiens P34931 32296183
种属内
TRIM38 O00635 HSPA2 Homo sapiens P54652 25416956
种属内
TRIM38 O00635 HSPA2 Homo sapiens P54652 31515488
种属内
TRIM38 O00635 HSPA2 Homo sapiens P54652 25416956
种属内
TRIM38 O00635 BYSL Homo sapiens Q13895 32296183
种属内
TRIM38 O00635 PSMA4 Homo sapiens P25789 32296183
种属内
TRIM38 O00635 PSMA4 Homo sapiens P25789 32296183
种属内
TRIM38 O00635 PIAS4 Homo sapiens Q8N2W9 32296183
种属内
TRIM38 O00635 PIAS4 Homo sapiens Q8N2W9 32296183
种属内
TRIM38 O00635 PIAS4 Homo sapiens Q8N2W9 32296183
种属内
TRIM38 O00635 TCEA2 Homo sapiens Q15560 32296183
种属内
TRIM38 O00635 RFC5 Homo sapiens P40937 25416956
种属内
TRIM38 O00635 RFC5 Homo sapiens P40937 32296183
种属内
TRIM38 O00635 RFC5 Homo sapiens P40937 25416956
种属内
TRIM38 O00635 RFC5 Homo sapiens P40937 25416956
种属内
TRIM38 O00635 RFC5 Homo sapiens P40937 29892012
种属内
TRIM38 O00635 RFC5 Homo sapiens P40937 31515488
种属内
TRIM38 O00635 SDCBP Homo sapiens O00560 25416956
种属内
TRIM38 O00635 SDCBP Homo sapiens O00560 25416956
种属内
TRIM38 O00635 GORASP2 Homo sapiens Q9H8Y8 25416956
种属内
TRIM38 O00635 GORASP2 Homo sapiens Q9H8Y8 32296183
种属内
TRIM38 O00635 ZNF764 Homo sapiens Q96H86 32296183
种属内
TRIM38 O00635 ATXN1 Homo sapiens P54253 23275563
种属内
TRIM38 O00635 ATXN1 Homo sapiens P54253 32814053
种属内
TRIM38 O00635 ATXN1 Homo sapiens P54253 32814053
种属内
TRIM38 O00635 ATXN1 Homo sapiens P54253 32814053
种属内
TRIM38 O00635 STXBP1 Homo sapiens P61764 32296183
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
Fanconi Renotubular Syndrome 2

FRTS2

Fanconi Renotubular Syndrome, Type 2

Acute Promyelocytic Leukemia

Leukemia, Acute Promyelocytic

Acute Myeloblastic Leukemia Type 3

Aml M3

APL

Leukemia, Acute Promyelocytic, Somatic

Aml With T(15

17)(Q22

Q12)

(Pml/Raralpha) And Variants

Apml

Acute Myeloblastic Leukemia 3

Acute Myeloid Leukemia With T(15

17)(Q22

Q12)

(Pml/Raralpha) And Variants

Acute Myeloblastic Leukaemia Type 3

Acute Myeloid Leukaemia M3

Acute Myeloid Leukemia M3

Acute Promyelocytic Leukaemia

M3 Anll

Myeloid Leukemia, Acute, M3

Leukemia Promyelocytic Acute

Leukemia, Promyelocytic, Acute

Leukemia, Acute, Promyelocytic

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
Macaca mulatta TRIM38 VGNC VGNC:78548
Bos taurus TRIM38 VGNC VGNC:36333
Rattus norvegicus TRIM38 RGD RGD:1596868
Canis familiaris TRIM38 VGNC VGNC:47819
Felis catus TRIM38 VGNC VGNC:66537
Mus musculus TRIM38 MGD MGI:2684869