1. Gene
  2. DCAF7 - DDB1 and CUL4 associated factor 7 Gene

DCAF7 - DDB1 and CUL4 associated factor 7 Gene

中文名称:DDB1 和 CUL4 相关因子 7

种属: Homo sapiens

同用名: AN11; HAN11; WDR68; SWAN-1

基因 ID: 10238 | 基因类型: protein coding

关于 DCAF7

Cytogenetic location: 17q23.3 Genomic coordinates (GRCh38): 17:63,550,477-63,594,266 (from NCBI)

This gene has 19 transcripts (splice variants) and 246 orthologues. Ubiquitous expression in kidney (RPKM 18.2), brain (RPKM 17.9) and 25 other tissues.

功能概要

该基因编码的蛋白质具有多个 WD40 重复序列,可促进蛋白质-蛋白质相互作用,从而实现多蛋白质复合物的组装。该蛋白质已被证明可作为参与激酶信号传导的蛋白质复合物的支架蛋白。这种高度保守的基因存在于真核植物、真菌和动物中。该基因的直系同源物首先在植物中被鉴定为花青素生物合成和花色素沉着的关键调节剂。可变剪接导致多个转录本变体。[RefSeq 提供,2014 年 2 月]

This gene encodes a protein with multiple WD40 repeats which facilitate protein-protein interactions and thereby enable the assembly of multiprotein complexes. This protein has been shown to function as a scaffold protein for protein complexes involved in kinase signaling. This highly conserved gene is present in eukaryotic Plants, fungi, and Animals. The ortholog of this gene was first identified in Plants as a key regulator of anthocyanin biosynthesis and flower pigmentation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]

DCAF7 基因产物(1)

mRNA Protein Name
NM_005828.5 NP_005819.3 DDB1- and CUL4-associated factor 7
基因本体论
  • 分子功能
  • 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
14593110 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of Cul4-RING E3 ubiquitin ligase complex IDA
IDA: 通过直接分析推断
16949367 GOA
located in nuclear matrix IDA
IDA: 通过直接分析推断
21328542 GOA
part of protein-containing complex IDA
IDA: 通过直接分析推断
21328542 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
蛋白主名 其他名称

DDB1- and CUL4-associated factor 7

WD repeat-containing protein 68

DCAF7 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
DCAF7 P61962 DYRK1A Homo sapiens Q13627
IF
20940704
种属内
DCAF7 P61962 DYRK1A Homo sapiens Q13627
Proximity Labelling
35016035
种属内
DCAF7 P61962 DYRK1A Homo sapiens Q13627
TAP
27705803
种属内
DCAF7 P61962 DYRK1A Homo sapiens Q13627
Anti Tag CoIP
35016035
种属内
DCAF7 P61962 DYRK1A Homo sapiens Q13627
Anti Tag CoIP
20940704
种属内
DCAF7 P61962 DYRK1A Homo sapiens Q13627
Anti Tag CoIP
33961781
种属内
DCAF7 P61962 DYRK1A Homo sapiens Q13627
TAP
27173435
种属内
DCAF7 P61962 ATN1 Homo sapiens Q86V38
Y2H Array
32814053
种属内
DCAF7 P61962 ATN1 Homo sapiens Q86V38
Y2H Pooling
32814053
种属内
DCAF7 P61962 ATN1 Homo sapiens Q86V38
Validated Y2H
32814053
种属内
DCAF7 P61962 LAMP2 Homo sapiens P13473-2
Validated Y2H
32814053
种属内
DCAF7 P61962 LAMP2 Homo sapiens P13473-2
Y2H Array
32814053
种属内
DCAF7 P61962 LAMP2 Homo sapiens P13473-2
Y2H Pooling
32814053
种属内
DCAF7 P61962 KLK6 Homo sapiens Q92876
Y2H Pooling
32814053
种属内
DCAF7 P61962 KLK6 Homo sapiens Q92876
Validated Y2H
32814053
种属内
DCAF7 P61962 KLK6 Homo sapiens Q92876
Y2H Array
32814053
种属内
DCAF7 P61962 HIPK2 Homo sapiens Q9H2X6
Anti Tag CoIP
20940704
种属内
DCAF7 P61962 HIPK2 Homo sapiens Q9H2X6
Anti Tag CoIP
33961781
种属内
DCAF7 P61962 HIPK2 Homo sapiens Q9H2X6
IF
20940704
种属内
DCAF7 P61962 TARDBP Homo sapiens Q13148
Validated Y2H
32814053
种属内
DCAF7 P61962 TARDBP Homo sapiens Q13148
Y2H Array
32814053
种属内
DCAF7 P61962 TARDBP Homo sapiens Q13148
Y2H Pooling
32814053
种属内
DCAF7 P61962 MAP3K1 Homo sapiens Q13233
IF
20940704
种属内
DCAF7 P61962 DYRK1B Homo sapiens Q9Y463
TAP
27705803
种属内
DCAF7 P61962 DYRK1B Homo sapiens Q9Y463
Anti Tag CoIP
35016035
种属内
DCAF7 P61962 DYRK1B Homo sapiens Q9Y463
Anti Tag CoIP
20940704
种属内
DCAF7 P61962 DYRK1B Homo sapiens Q9Y463
Anti Tag CoIP
33961781
种属内
DCAF7 P61962 CASP6 Homo sapiens P55212
Y2H Pooling
32814053
种属内
DCAF7 P61962 CASP6 Homo sapiens P55212
Validated Y2H
32814053
种属内
DCAF7 P61962 CASP6 Homo sapiens P55212
Y2H Array
32814053
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
Noonan Syndrome 4

NS4

Noonan Syndrome, Type 4

Abdominal Obesity-Metabolic Syndrome 3

AOMS3

Central Obesity, Type 2 Diabetes, Hypertension, And Early-Onset Coronary Artery Disease

Obesity, Abdominal, Metabolic Syndrome, Type 3

Intellectual Developmental Disorder, Autosomal Dominant 7

MRD7

Mental Retardation, Autosomal Dominant 7

Autosomal Dominant Non-Syndromic Intellectual Disability 7

Dyrk1a Syndrome

Autosomal Dominant Intellectual Developmental Disorder 7

Autosomal Dominant Mental Retardation 7

Mental Retardation, Autosomal Dominant, Type 7

Epidermodysplasia Verruciformis 1

Epidermodysplasia Verruciformis

Epidermodysplasia Verruciformis, Susceptibility To, 1

Lutz-Lewandowsky Epidermodysplasia Verruciformis

EV1

Lewandowsky-Lutz Syndrome

Ev

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
Rattus norvegicus DCAF7 RGD RGD:1305140
Bos taurus DCAF7 VGNC VGNC:27907
Mus musculus DCAF7 MGD MGI:1919083
Macaca mulatta DCAF7 VGNC VGNC:71820
Felis catus DCAF7 VGNC VGNC:61360
Canis familiaris DCAF7 VGNC VGNC:39796
Others DCAF7 NCBI