1. Gene
  2. SUV39H2 - SUV39H2 histone lysine methyltransferase Gene

SUV39H2 - SUV39H2 histone lysine methyltransferase Gene

中文名称:SUV39H2 组蛋白赖氨酸甲基转移酶

种属: Homo sapiens

同用名: KMT1B

基因 ID: 79723 | 基因类型: protein coding

关于 SUV39H2

Cytogenetic location: 10p13 Genomic coordinates (GRCh38): 10:14,878,866-14,904,315 (from NCBI)

This gene has 8 transcripts (splice variants), 145 orthologues and 19 paralogues. Broad expression in testis (RPKM 10.3), lymph node (RPKM 2.1) and 23 other tissues.

功能概要

启用 S-腺苷-L-甲硫氨酸结合活性;组蛋白甲基转移酶活性 (H3-K9 特异性) ;和锌离子结合活性。参与染色质组装或拆卸以及染色质重塑。在细胞对缺氧和 RNA 聚合酶 II 的转录负调节反应的上游或细胞内起作用。位于染色质中。 [由基因组资源联盟提供,2022 年 4 月]

Enables S-adenosyl-L-methionine binding activity; Histone Methyltransferase activity (H3-K9 specific); and zinc ion binding activity. Involved in chromatin assembly or disassembly and chromatin remodeling. Acts upstream of or within cellular response to hypoxia and negative regulation of transcription by RNA polymerase II. Located in chromatin. [provided by Alliance of Genome Resources, Apr 2022]

SUV39H2 基因产物(5)

mRNA Protein Name
NM_001193424.2 NP_001180353.1 histone-lysine N-methyltransferase SUV39H2 isoform 1
NM_001193425.2 NP_001180354.1 histone-lysine N-methyltransferase SUV39H2 isoform 2
NM_001193426.2 NP_001180355.1 histone-lysine N-methyltransferase SUV39H2 isoform 3
NM_001193427.2 NP_001180356.1 histone-lysine N-methyltransferase SUV39H2 isoform 4
NM_024670.4 NP_078946.1 histone-lysine N-methyltransferase SUV39H2 isoform 2
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 S-adenosyl-L-methionine binding IDA
IDA: 通过直接分析推断
20084102 GOA
enables histone H3K9 methyltransferase activity IDA
IDA: 通过直接分析推断
10949293 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
17474147 GOA
enables ubiquitin-like ligase-substrate adaptor activity IDA
IDA: 通过直接分析推断
30111536 GOA
enables zinc ion binding IDA
IDA: 通过直接分析推断
20084102 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
acts upstream of or within cellular response to hypoxia IDA
IDA: 通过直接分析推断
21402781 GOA
involved in chromatin organization IMP
IMP: 通过突变表型推断
10949293 GOA
involved in chromatin remodeling IDA
IDA: 通过直接分析推断
10949293 GOA
involved in epigenetic programming in the zygotic pronuclei IDA
IDA: 通过直接分析推断
30111536 GOA
acts upstream of or within negative regulation of transcription by RNA polymerase II IMP
IMP: 通过突变表型推断
21402781 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in chromatin IDA
IDA: 通过直接分析推断
10949293 GOA
is active in nucleus IDA
IDA: 通过直接分析推断
30111536 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

SUV39H2 蛋白结构

Chromo

Chromo: Chromo (CHRromatin Organisation MOdifier) domain (47 - 94)

Pre-SET

Pre-SET: Pre-SET motif (147 - 242)

SET

SET: SET domain (262 - 373)

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

histone-lysine N-methyltransferase SUV39H2

H3-K9-HMTase 2

SUV39H2 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
SUV39H2 Q9H5I1 HEL25 Homo sapiens V9HWG0 25416956
种属内
SUV39H2 Q9H5I1 PHF19 Homo sapiens Q5T6S3 23455924
种属内
SUV39H2 Q9H5I1 PHF19 Homo sapiens Q5T6S3
Y2H
23455924
种属内
SUV39H2 Q9H5I1 PNMA1 Homo sapiens Q8ND90 25416956
种属内
SUV39H2 Q9H5I1 NCK1 Homo sapiens P16333 17474147
种属内
SUV39H2 Q9H5I1 APPL2 Homo sapiens Q8NEU8 31515488
种属内
SUV39H2 Q9H5I1 APPL2 Homo sapiens Q8NEU8 25416956
种属内
SUV39H2 Q9H5I1 APPL2 Homo sapiens Q8NEU8 25416956
种属内
SUV39H2 Q9H5I1 KCTD17 Homo sapiens Q8N5Z5
Y2H
23455924
种属内
SUV39H2 Q9H5I1 KCTD17 Homo sapiens Q8N5Z5 23455924
种属内
SUV39H2 Q9H5I1 KLHDC4 Homo sapiens Q8TBB5 23455924
种属内
SUV39H2 Q9H5I1 KLHDC4 Homo sapiens Q8TBB5
Y2H
23455924
种属内
SUV39H2 Q9H5I1 MRFAP1 Homo sapiens Q9Y605
Y2H
23455924
种属间: 跨种属相互作用 种属内: 同种属相互作用

SUV39H2 抗体

目录号 产品名 应用 反应物种
HY-P82137 KMT1B Antibody (YA1882) WB, IHC-P, IP Human, Mouse, Rat

关联疾病

疾病名称 别名
Hyperoxaluria, Primary, Type I

Primary Hyperoxaluria Type 1

HP1

Glycolic Aciduria

Alanine-Glyoxylate Aminotransferase Deficiency

Hepatic Agt Deficiency

Oxalosis I

Primary Hyperoxaluria, Type I

Serine:Pyruvate Aminotransferase Deficiency

Hyperoxaluria, Primary, Type 1

Peroxisomal Alanine-Glyoxylate Aminotransferase Deficiency

Peroxisomal Alanine Glyoxylate Aminotransferase Deficiency

Serine Pyruvate Aminotransferase Deficiency

Peroxisomal Alanine:Glyoxylate Aminotransferase Deficiency

Oxalosis 1

Hyperoxaluria Primary 1

Hyperoxaluria Primary Type I

Ph1

Primary Hyperoxaluria Type I

Oxalosis Type 1

2-Oxoglutarate Glyoxylate Carboligase Deficiency

Primary Hyperoxaluria

Hyperoxaluria

Hyperoxaluria, Primary

Oxalosis

Primary Oxalosis

Congenital Oxaluria

D-Glycerate Dehydrogenase Deficiency

Glyceric Aciduria

Glycolic Aciduria

Hepatic Agt Deficiency

Oxaluria, Primary

Peroxisomal Alanine:Glyoxylate Aminotransferase Deficiency

Primary Oxaluria

Hyperoxaluria Primary

Primary Hyperoxaluria Type 2

Primary Hyperoxaluria, Type I

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
Bos taurus SUV39H2 VGNC VGNC:35492
Macaca mulatta SUV39H2 VGNC VGNC:103876
Rattus norvegicus SUV39H2 RGD RGD:1306969
Felis catus SUV39H2 VGNC VGNC:65858
Canis familiaris SUV39H2 VGNC VGNC:84435
Mus musculus SUV39H2 MGD MGI:1890396