2. Gene
  3. TRMT112 - tRNA methyltransferase activator subunit 11-2 Gene

TRMT112 - tRNA methyltransferase activator subunit 11-2 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：tRNA 甲基转移酶激活子亚基 11-2

种属: Homo sapiens

同用名: TRM112; HSPC152; HSPC170; hTrm112; TRMT11-2

基因 ID: 51504 | 基因类型: protein coding

关于 TRMT112

Cytogenetic location: 11q13.1 Genomic coordinates (GRCh38): 11:64,316,460-64,318,596 (from NCBI)

This gene has 6 transcripts (splice variants) and 217 orthologues. Ubiquitous expression in adrenal (RPKM 47.8), ovary (RPKM 46.2) and 25 other tissues.

功能概要

启用蛋白质异二聚化活性和蛋白质甲基转移酶活性。参与大分子甲基化和 rRNA 加工的正调控。位于细胞质的核质和核周区。部分含蛋白质复合物。 [由基因组资源联盟提供，2022 年 4 月]

Enables protein heterodimerization activity and protein methyltransferase activity. Involved in macromolecule methylation and positive regulation of rRNA processing. Located in nucleoplasm and perinuclear region of cytoplasm. Part of protein-containing complex. [provided by Alliance of Genome Resources, Apr 2022]

TRMT112 基因产物(5)

mRNA Protein Name
NM_001286082.2 NP_001273011.1 multifunctional methyltransferase subunit TRM112-like protein isoform 2
NM_001286084.2 NP_001273013.1 multifunctional methyltransferase subunit TRM112-like protein isoform 3
NM_001372071.1 NP_001359000.1 multifunctional methyltransferase subunit TRM112-like protein isoform 1
NM_001372072.1 NP_001359001.1 multifunctional methyltransferase subunit TRM112-like protein isoform 1
NM_016404.3 NP_057488.1 multifunctional methyltransferase subunit TRM112-like protein isoform 1

TRMT112 蛋白结构

Trm112p

Trm112p: Trm112p-like protein (2 - 112)

  • 0
  • 100
  • 125 a.a.
蛋白主名 其他名称

multifunctional methyltransferase subunit TRM112-like protein

TRM112-like protein

重组 TRMT112 蛋白

目录号 产品名 蛋白编号 纯度
HY-P71644 TRMT112 Protein, Human (His-SUMO) Q9UI30 (1M-125S) ≥95%

关联疾病

疾病名称 别名
Cardiomyopathy, Familial Restrictive, 1

RCM1

Restrictive Cardiomyopathy 1

Rcm

Familial Restrictive Cardiomyopathy 1

Cardiomyopathy, Familial Restrictive 1

Cardiomyopathy, Restrictive, Familial, Type 1

Rcm-1
Williams-Beuren Syndrome

Williams Syndrome

WBS

Wms

Deletion 7q11.23

Monosomy 7q11.23

Chromosome 7q11.23 Deletion Syndrome, 1.5- To 1.8-Mb

Fanconi Schlesinger Syndrome

Beuren Syndrome

Elfin Facies Syndrome

Elfin Facies With Hypercalcemia

Hypercalcemia-Supravalvar Aortic Stenosis

Ws
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS15090 TRMT112 Human Pre-designed siRNA Set A / 否

直系同源

种属 基因名 来源 基因 ID
Macaca mulatta TRMT112 VGNC VGNC:101420
Canis familiaris TRMT112 VGNC VGNC:47855
Felis catus TRMT112 VGNC VGNC:81099
Mus musculus TRMT112 MGD MGI:1914924
Rattus norvegicus TRMT112 RGD RGD:1309710
Others TRMT112 NCBI
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