1. Gene
  2. SUB1 - SUB1 regulator of transcription Gene

SUB1 - SUB1 regulator of transcription Gene

中文名称:SUB1 转录调节因子

种属: Homo sapiens

同用名: P15; PC4; p14

基因 ID: 10923 | 基因类型: protein coding

关于 SUB1

Cytogenetic location: 5p13.3 Genomic coordinates (GRCh38): 5:32,585,557-32,604,079 (from NCBI)

This gene has 13 transcripts (splice variants) and 228 orthologues. Ubiquitous expression in brain (RPKM 41.5), fat (RPKM 34.4) and 25 other tissues.

功能概要

实现相同的蛋白质结合活性;单链 DNA 结合活性;和转录共激活因子活性。参与 DNA 代谢过程的负调控和 RNA 聚合酶 II 的转录调控。位于核仁和核质中。转录调节复合物的一部分。 [由基因组资源联盟提供,2022 年 4 月]

Enables identical protein binding activity; single-stranded DNA binding activity; and transcription coactivator activity. Involved in negative regulation of DNA metabolic process and regulation of transcription by RNA polymerase II. Located in nucleolus and nucleoplasm. Part of transcription regulator complex. [provided by Alliance of Genome Resources, Apr 2022]

SUB1 基因产物(1)

mRNA Protein Name
NM_006713.4 NP_006704.3 activated RNA polymerase II transcriptional coactivator p15

SUB1 蛋白结构

PC4

PC4: Transcriptional Coactivator p15 (PC4) (63 - 116)

  • 0
  • 100
  • 127 a.a.
蛋白主名 其他名称

activated RNA polymerase II transcriptional coactivator p15

SUB1 homolog, transcriptional regulator

重组 SUB1 蛋白

目录号 产品名 蛋白编号 纯度
HY-P74650 PC4/SUB1 Protein, Human (His) P53999 (M1-L127) ≥95%

关联疾病

疾病名称 别名
Dyskeratosis Congenita, Autosomal Recessive 5

Dyskeratosis Congenita, Autosomal Dominant, 4

DKCB5

Autosomal Dominant Dyskeratosis Congenita 4

DKCA4

Autosomal Recessive Dyskeratosis Congenita 5

Dyskeratosis Congenita, Autosomal Recessive, 5

Dyskeratosis Congenita, Autosomal Dominant 4

Dyskeratosis Congenita, Autosomal Recessive, Type 5

Tinea Manuum

Tinea Manus

Dermatophytosis Of Hand

Cri-Du-Chat Syndrome

5p Deletion Syndrome

5p Partial Monosomy Syndrome

Monosomy 5p

Cat Cry Syndrome

Chromosome 5p Deletion Syndrome

Cri Du Chat Syndrome

5p- Syndrome

5p Minus Syndrome

Chromosome 5p- Syndrome

Chromosome 5 Short Arm Deletion Syndrome

Chromosome 5p Deletion

Deletion 5p

Cri Du Chat

5p Partial Deletion Syndrome

Partial Deletion Of Short Arm Of Chromosome 5 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
Mus musculus SUB1 MGD MGI:104811
Rattus norvegicus SUB1 RGD RGD:621582
Bos taurus SUB1 VGNC VGNC:35454
Macaca mulatta SUB1 VGNC VGNC:110431
Others SUB1 NCBI