1. Gene
  2. STAG2 - stromal antigen 2 Gene

STAG2 - stromal antigen 2 Gene

中文名称:基质抗原 2

种属: Homo sapiens

同用名: SA2; MKMS; SA-2; HPE13; SCC3B; NEDXCF; bA517O1.1

基因 ID: 10735 | 基因类型: protein coding

关于 STAG2

Cytogenetic location: Xq25 Genomic coordinates (GRCh38): X:123,960,560-124,102,656 (from NCBI)

This gene has 29 transcripts (splice variants), 203 orthologues, 2 paralogues and is associated with 138 phenotypes. Ubiquitous expression in thyroid (RPKM 24.4), bone marrow (RPKM 22.3) and 25 other tissues.

功能概要

该基因编码的蛋白质是 cohesin 复合物的一个亚基,它在细胞分裂过程中调节姐妹染色单体的分离。该基因的靶向失活会导致染色单体内聚缺陷和非整倍体,这表明内聚蛋白的遗传破坏是人类癌症中非整倍体的一个原因。已发现该基因编码不同亚型的可变剪接转录物变体。[RefSeq 提供,2013 年 9 月]

The protein encoded by this gene is a subunit of the cohesin complex, which regulates the separation of sister chromatids during cell division. Targeted inactivation of this gene results in chromatid cohesion defects and aneuploidy, suggesting that genetic disruption of cohesin is a cause of aneuploidy in human Cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]

STAG2 基因产物(17)

mRNA Protein Name
NM_001042749.2 NP_001036214.1 cohesin subunit SA-2 isoform a
NM_001042750.2 NP_001036215.1 cohesin subunit SA-2 isoform a
NM_001042751.2 NP_001036216.1 cohesin subunit SA-2 isoform b
NM_001282418.2 NP_001269347.1 cohesin subunit SA-2 isoform b
NM_001375366.1 NP_001362295.1 cohesin subunit SA-2 isoform a
NM_001375367.1 NP_001362296.1 cohesin subunit SA-2 isoform a
NM_001375368.1 NP_001362297.1 cohesin subunit SA-2 isoform a
NM_001375369.1 NP_001362298.1 cohesin subunit SA-2 isoform a
NM_001375370.1 NP_001362299.1 cohesin subunit SA-2 isoform a
NM_001375371.1 NP_001362300.1 cohesin subunit SA-2 isoform a
NM_001375372.1 NP_001362301.1 cohesin subunit SA-2 isoform a
NM_001375373.1 NP_001362302.1 cohesin subunit SA-2 isoform b
NM_001375374.1 NP_001362303.1 cohesin subunit SA-2 isoform b
NM_001375375.1 NP_001362304.1 cohesin subunit SA-2 isoform b
NM_001375376.1 NP_001362305.1 cohesin subunit SA-2 isoform b
NM_001375377.1 NP_001362306.1 cohesin subunit SA-2 isoform b
NM_006603.5 NP_006594.3 cohesin subunit SA-2 isoform b
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
15737063 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
involved in sister chromatid cohesion IMP
IMP: 通过突变表型推断
15917200 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
part of cohesin complex IMP
IMP: 通过突变表型推断
29263825 GOA
part of mitotic cohesin complex IPI
IPI: 通过物理相互作用推断
23242214 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

STAG2 蛋白结构

STAG

STAG: STAG domain (154 - 273)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1200
  • 1268 a.a.
蛋白主名 其他名称

cohesin subunit SA-2

SCC3 homolog 2

STAG2 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
Intra STAG2 Q8N3U4 WAPL Homo sapiens Q7Z5K2
Anti Tag CoIP
25173175
Intra STAG2 Q8N3U4 WAPL Homo sapiens Q7Z5K2
Pull Down
29263825
Intra STAG2 Q8N3U4 WAPL Homo sapiens Q7Z5K2
Anti Bait CoIP
29867216
Intra STAG2 Q8N3U4 WAPL Homo sapiens Q7Z5K2
Anti Tag CoIP
35271311
Intra STAG2 Q8N3U4 WAPL Homo sapiens Q7Z5K2
Anti Tag CoIP
29263825
Intra STAG2 Q8N3U4 WAPL Homo sapiens Q7Z5K2
Anti Bait CoIP
17113138
Intra STAG2 Q8N3U4 STAG1 Homo sapiens Q8WVM7
TAP
24981860
Intra STAG2 Q8N3U4 STAG1 Homo sapiens Q8WVM7
Anti Bait CoIP
29867216
Intra STAG2 Q8N3U4 STAG1 Homo sapiens Q8WVM7
Anti Bait CoIP
17962804
Intra STAG2 Q8N3U4 PDS5A Homo sapiens Q29RF7
Anti Bait CoIP
29867216
Intra STAG2 Q8N3U4 PDS5A Homo sapiens Q29RF7
Anti Tag CoIP
29263825
Intra STAG2 Q8N3U4 PDS5A Homo sapiens Q29RF7
Anti Bait CoIP
17113138
Intra STAG2 Q8N3U4 PDS5A Homo sapiens Q29RF7
Anti Tag CoIP
35271311
Intra STAG2 Q8N3U4 PDS5B Homo sapiens Q9NTI5
Anti Bait CoIP
15855230
Intra STAG2 Q8N3U4 PDS5B Homo sapiens Q9NTI5
Anti Bait CoIP
29867216
Intra STAG2 Q8N3U4 PDS5B Homo sapiens Q9NTI5
Anti Bait CoIP
17113138
Intra STAG2 Q8N3U4 SSU72 Homo sapiens Q9NP77
Pull Down
20818333
Intra STAG2 Q8N3U4 SMC1A Homo sapiens Q14683
Anti Bait CoIP
19629043
Intra STAG2 Q8N3U4 SMC1A Homo sapiens Q14683
Anti Bait CoIP
17113138
Intra STAG2 Q8N3U4 SMC1A Homo sapiens Q14683
Anti Tag CoIP
29263825
Intra STAG2 Q8N3U4 SMC1A Homo sapiens Q14683
Anti Tag CoIP
35271311
Intra STAG2 Q8N3U4 SMC1A Homo sapiens Q14683
TAP
24981860
Intra STAG2 Q8N3U4 SMC1A Homo sapiens Q14683
Anti Bait CoIP
29867216
Intra STAG2 Q8N3U4 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
22885700
Intra STAG2 Q8N3U4 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
19629043
Intra STAG2 Q8N3U4 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
17962804
Intra STAG2 Q8N3U4 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
17113138
Intra STAG2 Q8N3U4 SMC3 Homo sapiens Q9UQE7
Anti Tag CoIP
35271311
Intra STAG2 Q8N3U4 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
29867216
Intra STAG2 Q8N3U4 SMC3 Homo sapiens Q9UQE7
TAP
24981860
Intra STAG2 Q8N3U4 SMC3 Homo sapiens Q9UQE7
Anti Bait CoIP
15855230
Intra STAG2 Q8N3U4 SMC3 Homo sapiens Q9UQE7
Anti Tag CoIP
29263825
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
Anti Bait CoIP
19629043
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
Anti Bait CoIP
17962804
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
Anti Bait CoIP
17113138
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
X-Ray Diffraction
25173175
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
Anti Tag CoIP
35271311
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
Anti Bait CoIP
22885700
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
Anti Bait CoIP
29867216
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
TAP
24981860
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
Pull Down
29263825
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
GMS
25173175
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
Anti Tag CoIP
29263825
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
Pull Down
25173175
Intra STAG2 Q8N3U4 RAD21 Homo sapiens O60216
Anti Tag CoIP
25173175
Intra STAG2 Q8N3U4 SGO1 Homo sapiens Q5FBB7
Pull Down
29263825
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
Mullegama-Klein-Martinez Syndrome

MKMS

Nedxcf

Neurodevelopmental Disorder, X-Linked, With Craniofacial Abnormalities

X-Linked Neurodevelopmental Disorder With Craniofacial Abnormalities

Holoprosencephaly 13, X-Linked

HPE13

Alobar Holoprosencephaly
Semilobar Holoprosencephaly
Chromosome Xq25 Duplication Syndrome

Xq25 Microduplication Syndrome

Xq25 Duplication Syndrome

Dup

Xq25 Microtriplication

Cornelia De Lange Syndrome

De Lange Syndrome

Brachmann De Lange Syndrome

Brachmann-De Lange Syndrome

Cdls

Bdls

Typus Degenerativus Amstelodamensis

Holoprosencephaly

Holoprosencephaly Sequence

Hpe

Hpe - [Holoprosencephaly]

Laryngotracheitis
Acute Myeloid Leukemia With Bcr-Abl1

Acute Myeleoid Leukemia With Bcr-Abl1

Septooptic Dysplasia

Septo-Optic Dysplasia

De Morsier Syndrome

Growth Hormone Deficiency With Pituitary Anomalies

SOD

Pituitary Hormone Deficiency, Combined, 5

Septo-Optic Dysplasia Spectrum

Septo-Optic Dysplasia With Growth Hormone Deficiency

Pituitary Hormone Deficiency, Combined 5

Hypopituitarism And Septooptic 'Dysplasia'

GHDPA

CPHD5

Dysplasia, Septo-Optic

Kallmann Syndrome

Breast Juvenile Papillomatosis

Juvenile Papillomatosis Of The Breast

Bladder Urothelial Carcinoma

Bladder Transitional Cell Carcinoma

Transitional Cell Carcinoma Of Bladder

Transitional Cell Carcinoma Of The Bladder

Urinary Bladder Urothelial Carcinoma

Urothelial Bladder Carcinoma

Carcinoma Transitional Cell Bladder

Tcc - [Transitional Cell Carcinoma] Of Bladder

Holoprosencephaly 7

HPE7

Holoprosencephaly-7

Holoprosencephaly, Type 7

Microcephaly

Microencephaly

Microcephalus

Microcephalic

Nanocephaly

Congenital Microcephaly

Brain Hypoplasia

Brain Nondevelopment

Cephalic Hypoplasia

Undeveloped Cerebrum

Undeveloped Brain

Micrencephalon

Micrencephaly

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

Immunodeficiency 21

Monocytopenia And Mycobacterial Infection Syndrome

Monomac

Gata2 Deficiency

Monocytopenia With Susceptibility To Infections

Dcml

IMD21

Dendritic Cell, Monocyte, B Lymphocyte, And Natural Killer Lymphocyte Deficiency

Monocytopenia With Susceptibility To Mycobacterial, Fungal, And Papillomavirus Infections And Myelodysplasia

Combined Immunodeficiency With Susceptibility To Mycobacterial, Viral, And Fungal Infections

Combined Immunodeficiency With Susceptibility To Mycobacterial, Viral And Fungal Infections

Dendritic Cell, Monocyte, B And Nk Lymphoid Deficiency

Monocyte-B-Natural Killer-Dendritic Cell Deficiency Syndrome

Monocytopenia With Mycobacterial, Fungal, And Papillomavirus Infections And Myelodysplasia

Combined Immunodeficiency With Mycobacterial, Viral, And Fungal Infections

Monocyte - B - Natural Killer - Dendritic Cell Deficiency

Combined Immunodeficiency With Susceptibility To Mycobacterial Viral And Fungal Infections

Dendritic Cell Monocyte Lymphocyte B And Natural Killer Lymphocyte Deficiency

Monocytopenia With Susceptibility To Mycobacterial Fungal And Papillomavirus Infections And Myelodysplasia

Bladder Cancer

Urinary Bladder Cancer

Bladder Carcinoma

Urinary Bladder Carcinoma

Bladder Neoplasm

Bladder Tumor

Cancer, Bladder

Malignant Neoplasm Of Urinary Bladder

Carcinoma Of Bladder

Bladder Cancer, Somatic

Tumor Of The Bladder

Carcinoma Of Urinary Bladder

Bladder Carcinoma Urinary

Cancer Of The Urinary Bladder

Cancer, Urinary Bladder

Malignant Bladder Neoplasm

Malignant Bladder Tumor

Neoplasm Of The Bladder

Neoplasm Of The Urinary Bladder

Tumor Of The Urinary Bladder

Urinary Bladder Neoplasm

BLC

Urothelial Carcinoma Of The Bladder

Bladder Tumors

Urinary Bladder Neoplasms

Bladder Cancer Nos

Vesical Cancer Nos

Malignant Neoplasm Of Bladder, Part Unspecified

Malignant Tumour Of Urinary Bladder

Primary Malignant Neoplasm Of Bladder

Chronic Myelomonocytic Leukemia

Leukemia, Myelomonocytic, Chronic

Cmml

Leukemia Myelomonocytic Chronic

Cmml - [Chronic Myelomonocytic Leukaemia]

Chronic Myelomonocytic Leukaemia Without Mention Of Remission

Chronic Monocytic Leukaemia

Chronic Monocytoid Leukaemia

Fanconi Anemia, Complementation Group A

Fanconi Anemia

Fanconi Pancytopenia

Fanconi Anemia Complementation Group A

FANCA

Fa

Fanconi Panmyelopathy

Fanconi'S Anemia

Fanconi Anaemia

Fanconi'S Anaemia

Fanconi Hypoplastic Anemia

Estren-Dameshek Variant Of Fanconi Anemia

Estren-Dameshek Variant Of Fanconi Pancytopenia

Fanconi Anemia Estren-Dameshek Variant

Fanconis Anemia

Ewing Sarcoma

Neuroepithelioma

Ewing'S Tumor

Primitive Neuroectodermal Tumor

Ewings Sarcoma

Ewing'S Sarcoma

Peripheral Neuroepithelioma

ES

Ewings Sarcoma-Primitive Neuroectodermal Tumor

Localized Peripheral Primitive Neuroectodermal Tumor

Peripheral Primitive Neuroectodermal Tumor

Ewing Tumor

Sarcoma, Ewing'S

Ewing Family Of Tumors

Extraosseous Ewing Tumor

Askin Tumor

Ewing'S Family Localized Tumor

Ewing'S Sarcoma/Peripheral Primitive Neuroectodermal Tumor

Localized Ewing Sarcoma

Localized Ewing'S Sarcoma

Localized Ewing'S Sarcoma/Peripheral Primitive Neuroectodermal Tumor

Localized Ewing'S Tumor

Pnet Of Thoracopulmonary Region

Tumor Of The Ewing Family

Skeletal Ewing Sarcoma

Osseous Ewing Sarcoma

Ppnet

Peripheral Pnet

Extraskeletal Ewing Sarcoma

Eoe

Extraosseous Ewing Sarcoma

Extraskeletal Ewing Tumor

Esft

Ewing Sarcoma Family Of Tumors

Pne

Pnet

Pnet Of The Chest Wall

Sarcoma, Ewing

Neuroectodermal Tumors, Primitive, Peripheral

Neuroectodermal Tumor, Primitive

Disorder Of Eye

Askin'S Tumor

Extraosseous Ewings Sarcoma-Primitive Neuroepithelial Tumor

Neuroepithelioma, Peripheral

Myelodysplastic Syndrome

Myelodysplastic Syndromes

Myelodysplasia

MDS

Myelodysplastic Syndrome Included

Myelodysplastic Syndrome, Susceptibility To, Included

Myelodysplastic Syndrome, Somatic

Myelodysplastic Syndrome, Susceptibility To

Leukemia, Acute Myeloid

Acute Myeloid Leukemia

Leukemia, Acute Myelogenous

Acute Myelogenous Leukemia

AML

Leukemia, Acute Myeloid, Susceptibility To

Acute Myeloblastic Leukemia

Leukemia, Acute Myeloid, Reduced Survival In, Somatic

Acute Myeloid Leukaemia

Leukemia, Myelocytic, Acute

Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

Secondary Aml

Acute Myelocytic Leukemia

Acute Myeloid Leukemia, Somatic

Leukemia, Acute Myeloid, Somatic

Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

Acute Myeloblastic Leukaemia

Acute Myelogenous Leukaemia

Aml - Acute Myeloid Leukemia

Acute Myeloid Leukemia With Cebpa Somatic Mutations

Aml With Cebpa Somatic Mutations

Inherited Acute Myeloid Leukemia

Familial Aml

Inherited Aml

Pure Familial Aml

Pure Familial Acute Myeloid Leukemia

Secondary Acute Myeloid Leukemia

Therapy-Related Aml And Myelodysplastic Syndrome

Acute Myeloid Leukemia, Secondary

Acute Non-Lymphoblastic Leukemia

Acute Non-Lymphocytic Leukemia

Acute Biphenotypic Leukemia

Acute Undifferentiated Leukemia

Acute Myeloblastic Leukaemia With Multilineage Dysplasia

Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

Acute Myeloid Leukaemia With Myelodysplasia-Related Features

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
Felis catus STAG2 VGNC VGNC:65744
Rattus norvegicus STAG2 RGD RGD:1562042
Mus musculus STAG2 MGD MGI:1098583
Bos taurus STAG2 VGNC VGNC:35354
Canis familiaris STAG2 VGNC VGNC:46874