1. Gene
  2. STAG1 - stromal antigen 1 Gene

STAG1 - stromal antigen 1 Gene

中文名称:基质抗原 1

种属: Homo sapiens

同用名: SA1; MRD47; SCC3A

基因 ID: 10274 | 基因类型: protein coding

关于 STAG1

Cytogenetic location: 3q22.3 Genomic coordinates (GRCh38): 3:136,336,236-136,752,378 (from NCBI)

This gene has 10 transcripts (splice variants), 221 orthologues, 2 paralogues and is associated with 88 phenotypes. Ubiquitous expression in ovary (RPKM 10.7), endometrium (RPKM 9.9) and 25 other tissues.

功能概要

该基因是 SCC3 家族的成员,在细胞核中表达。它编码 cohesin 的一个成分,cohesin 是一种多亚基蛋白复合物,从 DNA 复制到前期和前中期,沿着染色体的长度提供姐妹染色单体的凝聚力,之后它被解离,为后期的分离做准备。[RefSeq 提供,2008 年 7 月]

This gene is a member of the SCC3 family and is expressed in the nucleus. It encodes a component of cohesin, a multisubunit protein complex that provides sister chromatid cohesion along the length of a chromosome from DNA replication through prophase and prometaphase, after which it is dissociated in preparation for segregation during anaphase. [provided by RefSeq, Jul 2008]

STAG1 基因产物(1)

mRNA Protein Name
NM_005862.3 NP_005853.2 cohesin subunit SA-1
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 protein binding IPI
IPI: 通过物理相互作用推断
15855230 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in mitotic spindle assembly IMP
IMP: 通过突变表型推断
11590136 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
16682347 GOA
part of cohesin complex IDA
IDA: 通过直接分析推断
11590136 GOA
located in mitotic spindle pole IDA
IDA: 通过直接分析推断
11590136 GOA
located in nuclear matrix IDA
IDA: 通过直接分析推断
11590136 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

STAG1 蛋白结构

STAG

STAG: STAG domain (157 - 276)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1258 a.a.
蛋白主名 其他名称

cohesin subunit SA-1

SCC3 homolog 1

STAG1 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
STAG1 Q8WVM7 STAG2 Homo sapiens Q8N3U4
Anti Bait CoIP
29867216
种属内
STAG1 Q8WVM7 STAG2 Homo sapiens Q8N3U4
Anti Tag CoIP
35271311
种属内
STAG1 Q8WVM7 STAG2 Homo sapiens Q8N3U4
Crosslink
30021884
种属内
STAG1 Q8WVM7 PDS5A Homo sapiens Q29RF7
Anti Bait CoIP
17113138
种属内
STAG1 Q8WVM7 PDS5B Homo sapiens Q9NTI5
Anti Bait CoIP
29867216
种属内
STAG1 Q8WVM7 PDS5B Homo sapiens Q9NTI5
Anti Bait CoIP
17113138
种属内
STAG1 Q8WVM7 TERF1 Homo sapiens P54274
Pull Down
17962804
种属内
STAG1 Q8WVM7 TERF1 Homo sapiens P54274
Anti Tag CoIP
17962804
种属内
STAG1 Q8WVM7 TERF1 Homo sapiens P54274
Anti Bait CoIP
17962804
种属内
STAG1 Q8WVM7 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
22885700
种属内
STAG1 Q8WVM7 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
15855230
种属内
STAG1 Q8WVM7 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
17962804
种属内
STAG1 Q8WVM7 SMC3 Homo sapiens Q9UQE7
Anti Tag CoIP
35271311
种属内
STAG1 Q8WVM7 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
17112726
种属内
STAG1 Q8WVM7 SMC3 Homo sapiens Q9UQE7
Pull Down
17962804
种属内
STAG1 Q8WVM7 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
29867216
种属内
STAG1 Q8WVM7 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
17113138
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
Intellectual Developmental Disorder, Autosomal Dominant 47

Mental Retardation, Autosomal Dominant 47

MRD47

Autosomal Dominant Intellectual Developmental Disorder 47

Autosomal Dominant Mental Retardation 47

Stag1-Related Intellectual Disability-Facial Dysmorphism-Gastroesophageal Reflux Syndrome

Cornelia De Lange Syndrome

De Lange Syndrome

Brachmann De Lange Syndrome

Brachmann-De Lange Syndrome

Cdls

Bdls

Typus Degenerativus Amstelodamensis

Amelogenesis Imperfecta, Type If

Amelogenesis Imperfecta Type 1f

AI1F

Amelogenesis Imperfecta, Hypoplastic Type If

Amelogenesis Imperfecta Type If

Amelogenesis Imperfecta Hypoplastic Type If

Amelogenesis Imperfecta 1f

Roberts-Sc Phocomelia Syndrome

Roberts Syndrome

Sc Phocomelia Syndrome

RBS

Long Bone Deficiencies Associated With Cleft Lip-Palate

Sc Pseudothalidomide Syndrome

Appelt-Gerken-Lenz Syndrome

Pseudothalidomide Syndrome

Tetraphocomelia-Cleft Palate Syndrome

Hypomelia Hypotrichosis Facial Hemangioma Syndrome

Roberts Syndrome/Sc Phocomelia

Roberts Tetraphocomelia Syndrome

Sc Syndrome

Sc Phocomelia

Sc Disease

Sc

Hemoglobin Sc Disease

Atrial Septal Defect 1

ASD1

Atrial Heart Septal Defect 1

Asd

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 STAG1 VGNC VGNC:46873
Felis catus STAG1 VGNC VGNC:82509
Rattus norvegicus STAG1 RGD RGD:1310744
Mus musculus STAG1 MGD MGI:1098658
Bos taurus STAG1 VGNC VGNC:35353
Macaca mulatta STAG1 VGNC VGNC:77901