2. Gene
  3. SLX4 - SLX4 structure-specific endonuclease subunit Gene

SLX4 - SLX4 structure-specific endonuclease subunit Gene

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

中文名称：SLX4 结构特异性核酸内切酶亚基

种属: Homo sapiens

同用名: FANCP; BTBD12; MUS312

基因 ID: 84464 | 基因类型: protein coding

关于 SLX4

Cytogenetic location: 16p13.3 Genomic coordinates (GRCh38): 16:3,581,181-3,611,606 (from NCBI)

This gene has 5 transcripts (splice variants), 208 orthologues and is associated with 4 phenotypes. Broad expression in testis (RPKM 5.9), lymph node (RPKM 2.0) and 22 other tissues.

功能概要

该基因编码的蛋白质可作为多种结构特异性核酸内切酶的组装成分。这些核酸内切酶复合物是修复特定类型的 DNA 损伤所必需的，并且对于细胞对复制叉失败的反应至关重要。在患有范可尼贫血的患者中发现了该基因的突变。[RefSeq 提供，2016 年 9 月]

This gene encodes a protein that functions as an assembly component of multiple structure-specific endonucleases. These Endonuclease complexes are required for repair of specific types of DNA lesions and critical for cellular responses to replication fork failure. Mutations in this gene were found in patients with Fanconi anemia. [provided by RefSeq, Sep 2016]

SLX4 基因产物(1)

mRNA Protein Name
NM_032444.4 NP_115820.2 structure-specific endonuclease subunit SLX4
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 enzyme activator activity IDA
IDA: 通过直接分析推断
19596235 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
19595721 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in DNA double-strand break processing involved in repair via single-strand annealing IMP
IMP: 通过突变表型推断
19595721 GOA
involved in DNA repair IMP
IMP: 通过突变表型推断
19595722 GOA
involved in double-strand break repair via homologous recombination IMP
IMP: 通过突变表型推断
19595721 GOA
involved in negative regulation of telomere maintenance via telomere lengthening IMP
IMP: 通过突变表型推断
24012755 GOA
involved in nucleotide-excision repair IMP
IMP: 通过突变表型推断
19596236 GOA
involved in positive regulation of telomere maintenance IDA
IDA: 通过直接分析推断
24012755 GOA
acts upstream of or within response to intra-S DNA damage checkpoint signaling IMP
IMP: 通过突变表型推断
23361013 GOA
involved in t-circle formation IMP
IMP: 通过突变表型推断
24012755 GOA
involved in telomeric D-loop disassembly IMP
IMP: 通过突变表型推断
24012755 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of ERCC4-ERCC1 complex IDA
IDA: 通过直接分析推断
19595721 GOA
part of Holliday junction resolvase complex IDA
IDA: 通过直接分析推断
19595721 GOA
part of Slx1-Slx4 complex IDA
IDA: 通过直接分析推断
19595721 GOA
located in chromatin IDA
IDA: 通过直接分析推断
19596235 GOA
colocalizes with chromosome, telomeric region IDA
IDA: 通过直接分析推断
19596235 GOA
located in chromosome, telomeric region IDA
IDA: 通过直接分析推断
24012755 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

SLX4 蛋白结构

BTB

BTB: BTB/POZ domain (685 - 788)

Slx4

Slx4: Slx4 endonuclease (1753 - 1810)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1500
  • 1834 a.a.
蛋白主名 其他名称

structure-specific endonuclease subunit SLX4

BTB/POZ domain-containing protein 12

SLX4 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 SLX4 Q8IY92 ERCC4 Homo sapiens Q92889
Anti Bait CoIP
19596235
Intra SLX4 Q8IY92 ERCC4 Homo sapiens Q92889
Anti Tag CoIP
19596235
Intra SLX4 Q8IY92 ERCC4 Homo sapiens Q92889
Anti Tag CoIP
19596236
Intra SLX4 Q8IY92 MUS81 Homo sapiens Q96NY9
Anti Tag CoIP
19596235
Intra SLX4 Q8IY92 MUS81 Homo sapiens Q96NY9
Validated Y2H
32296183
Intra SLX4 Q8IY92 MUS81 Homo sapiens Q96NY9
Anti Bait CoIP
19596235
Intra SLX4 Q8IY92 EME1 Homo sapiens Q96AY2
Anti Tag CoIP
19596235
Intra SLX4 Q8IY92 EME1 Homo sapiens Q96AY2
Anti Tag CoIP
19596236
Intra SLX4 Q8IY92 SLX1A Homo sapiens Q9BQ83
Anti Tag CoIP
19596235
Intra SLX4 Q8IY92 SLX1A Homo sapiens Q9BQ83
Y2H
19596235
Intra SLX4 Q8IY92 SLX1A Homo sapiens Q9BQ83
Anti Tag CoIP
19596236
Intra SLX4 Q8IY92 SLX4IP Homo sapiens Q5VYV7
Anti Tag CoIP
19596235
Intra SLX4 Q8IY92 MSH2 Homo sapiens P43246
Anti Tag CoIP
19596235
Intra SLX4 Q8IY92 MSH2 Homo sapiens P43246
Anti Bait CoIP
19596235
Intra SLX4 Q8IY92 PLK1 Homo sapiens P53350
Anti Bait CoIP
19596235
Intra SLX4 Q8IY92 PLK1 Homo sapiens P53350
Anti Tag CoIP
19596235
Intra SLX4 Q8IY92 TERF2 Homo sapiens Q15554
Anti Bait CoIP
19596235
Intra SLX4 Q8IY92 TERF2 Homo sapiens Q15554
Anti Tag CoIP
19596236
Intra SLX4 Q8IY92 TERF2 Homo sapiens Q15554
Anti Tag CoIP
19596235
Intra SLX4 Q8IY92 TERF2IP Homo sapiens Q9NYB0
Anti Bait CoIP
19596235
Intra SLX4 Q8IY92 TERF2IP Homo sapiens Q9NYB0
Anti Tag CoIP
19596235
Intra SLX4 Q8IY92 ERCC1 Homo sapiens P07992
Anti Tag CoIP
19596236
Intra SLX4 Q8IY92 ERCC1 Homo sapiens P07992
Anti Tag CoIP
19596235
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
Fanconi Anemia, Complementation Group P

Fanconi Anemia Complementation Group P

FANCP
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
Papillary Adenofibroma
Fanconi Anemia, Complementation Group V

Fanconi Anemia Complementation Group V

FANCV
Fanconi Anemia, Complementation Group R

Fanconi Anemia Complementation Group R

FANCR
Fanconi Anemia, Complementation Group Q

Fanconi Anemia Complementation Group Q

FANCQ
Xfe Progeroid Syndrome

Xpf-Ercc1 Progeroid Syndrome

XFEPS
Fanconi Anemia, Complementation Group O

Fanconi Anemia Complementation Group O

FANCO
Interstitial Nephritis, Karyomegalic

Karyomegalic Interstitial Nephritis

KMIN

Kin

Systemic Karyomegaly

Karyomegalic Tubulointerstitial Nephritis

Ktn
Glioblastoma

Glioblastoma Multiforme

Gbm

Adult Glioblastoma Multiforme

Grade Iv Adult Astrocytic Tumor

Primary Glioblastoma Multiforme

Spongioblastoma Multiforme

Adult Glioblastoma

Primary Glioblastoma
Xeroderma Pigmentosum, Complementation Group F

Xeroderma Pigmentosum, Group F

Xeroderma Pigmentosum Vi

Xp6

Xeroderma Pigmentosum, Type F/Cockayne Syndrome

XPF

Xp, Group F

Xeroderma Pigmentosum Group F

Xp Group F

Xeroderma Pigmentosum, Type 6

Xeroderma Pigmentosum Complementation Group F

XP-F

Xeroderma Pigmentosum Type F/Cockayne Syndrome

XPF/CS
Fanconi Anemia, Complementation Group D1

Fanconi Anemia Complementation Group D1

FANCD1

Fad1

Inherited Cancer-Predisposing Syndrome Due To Biallelic Brca2 Mutations
Xeroderma Pigmentosum, Variant Type

Xeroderma Pigmentosum

XPV

Xeroderma Pigmentosum Variant Type

Xeroderma Pigmentosum With Normal Dna Repair Rates

Photosensitivity With Defective Dna Synthesis

Xp

De Sanctis-Cacchione Syndrome

Desanctis-Cacchione Syndrome

Xeroderma Pigmentosa

Xerodermic Idiocy

Xeroderma Pigmentosum Variant

Xp - [Xeroderma Pigmentosum]

Atrophoderma Pigmentosum
Cerebrooculofacioskeletal Syndrome

Cerebro-Oculo-Facio-Skeletal Syndrome

Cofs Syndrome

Pena-Shokeir Syndrome Type 2

Pena Shokeir Syndrome Type 2
Xeroderma Pigmentosum, Complementation Group G

Xeroderma Pigmentosum, Group G

Xeroderma Pigmentosum Vii

Xp7

XPG

Xeroderma Pigmentosum Group G

Xp Group G

Xp, Group G

Xpgc

Xeroderma Pigmentosum, Group G/Cockayne Syndrome

Xeroderma Pigmentosum, Type 7

Xeroderma Pigmentosum Complementation Group G

XP-G

Xp-G/Cs

Xeroderma Pigmentosum Group G/Cockayne Syndrome
Physical Disorder

Physical Illness
Aplastic Anemia

Aplastic Anemia, Susceptibility To

Anemia Aplastic

Idiopathic Aplastic Anemia

Secondary Aplastic Anemia

Idiopathic Bone Marrow Failure

Aplastic Anemia Idiopathic

AA

Anemia, Aplastic

Aplastic Anemia, Idiopathic

Erythroid Aplasia

Aa - [Aplastic Anaemia]

Haematopoietic Aplasia

Aleukia Haemorrhagica

Anaemia Due To Decreased Red Cell Production

Aplasia Bone Marrow

Aplastic Bone Marrow

Hypoplastic Anaemia Nos

Myeloid Bone Marrow Aplasia

Pancytopenia

Panhaematopenia

Hypoproliferative Anaemia

Medullary Hypoplasia

Red Blood Cells Hypoplastic Anaemia

Panmyelophthisis

Panhemocytopenia

Refractive Hypoproliferative Anaemia

Toxic Anaemia

Toxic Aplastic Anaemia

Aplastic Anaemia Due To Toxic Cause

Idiopathic Aplastic Anaemia Nos
Dyskeratosis Congenita

Dyskeratosis Congenita Autosomal Dominant

Dc

Dkc

Zinsser-Engman-Cole Syndrome

Dyskeratosis Congenita, Autosomal Dominant

Autosomal Dominant Dyskeratosis Congenita

Dkca

Dyskeratosis Congenita Scoggins Type

Zinsser-Cole-Engman Syndrome

X-Linked Dyskeratosis Congenita

Hoyeraal-Hreidarsson Syndrome
Hereditary Breast Ovarian Cancer Syndrome

Hereditary Breast And Ovarian Cancer Syndrome

Brca1- And Brca2-Associated Hereditary Breast And Ovarian Cancer

Breast And/Or Ovarian Cancer

Breast And Ovarian Cancer Syndrome

Hboc Syndrome

Hereditary Breast And Ovarian Cancer

Brca1- Brca2-Associated Hboc
Seckel Syndrome

Microcephalic Primordial Dwarfism

Bird-Headed Dwarfism

Harper'S Syndrome

Virchow-Seckel Dwarfism

Nanocephalic Dwarfism

Sckl

Seckel-Type Dwarfism
Deficiency Anemia

Anemia

Deficiency Anemias

Anaemia
Lynch Syndrome

Hereditary Nonpolyposis Colon Cancer

Hereditary Nonpolyposis Colorectal Cancer

Hereditary Nonpolyposis Colorectal Carcinoma

Hereditary Nonpolyposis Colorectal Neoplasms

Familial Nonpolyposis Colon Cancer

Hnpcc

Coca 1

Hereditary Defective Mismatch Repair Syndrome

Hereditary Non-Polyposis Colon Cancer

Hereditary Non-Polyposis Colon Cancer Syndrome

Hereditary Non-Polyposis Colorectal Cancer

Hereditary Non-Polyposis Colorectal Cancer Syndrome

Hereditary Nonpolyposis Colon Cancer Syndrome

Hereditary Nonpolyposis Colorectal Cancer Syndrome

Hereditary Nonpolyposis Colorectal Neoplasm

Hnpcc - Hereditary Nonpolyposis Colon Cancer

Cancer Family Syndrome

Familial Nonpolyposis Colorectal Cancer

Colon Cancer, Familial Nonpolyposis

Colorectal Neoplasms, Hereditary Nonpolyposis

Cancer, Colorectal, Nonpolyposis, Hereditary

Colorectal Cancer, Hereditary Nonpolyposis, Type 1
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 (2)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS13389 SLX4 Human Pre-designed siRNA Set A Pre-designed Sets / 否
HY-RS13390 SLX4IP Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Macaca mulatta SLX4 VGNC VGNC:99590
Bos taurus SLX4 VGNC VGNC:34973
Rattus norvegicus SLX4 RGD RGD:1566009
Mus musculus SLX4 MGD MGI:106299
Canis familiaris SLX4 VGNC VGNC:46517
Felis catus SLX4 VGNC VGNC:65458
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