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

DCAF7 - DDB1 and CUL4 associated factor 7 Gene

Homo sapiens

Also known as AN11; HAN11; WDR68; SWAN-1

Gene ID: 10238 | Gene type: protein coding

About 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.

Summary

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 Products(1)

mRNA Protein Name
NM_005828.5 NP_005819.3 DDB1- and CUL4-associated factor 7
Gene Ontology
  • Molecular Function
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
14593110 GOA
Cellular Component GO Annotation Evidence Reference Source
part of Cul4-RING E3 ubiquitin ligase complex IDA
IDA: Inferred from direct assay
16949367 GOA
located in nuclear matrix IDA
IDA: Inferred from direct assay
21328542 GOA
part of protein-containing complex IDA
IDA: Inferred from direct assay
21328542 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

DDB1- and CUL4-associated factor 7

WD repeat-containing protein 68

DCAF7 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
DCAF7 P61962 DYRK1A Homo sapiens Q13627
IF
20940704
Intra
DCAF7 P61962 DYRK1A Homo sapiens Q13627 35016035
Intra
DCAF7 P61962 DYRK1A Homo sapiens Q13627
TAP
27705803
Intra
DCAF7 P61962 DYRK1A Homo sapiens Q13627 35016035
Intra
DCAF7 P61962 DYRK1A Homo sapiens Q13627 20940704
Intra
DCAF7 P61962 DYRK1A Homo sapiens Q13627 33961781
Intra
DCAF7 P61962 DYRK1A Homo sapiens Q13627
TAP
27173435
Intra
DCAF7 P61962 ATN1 Homo sapiens Q86V38 32814053
Intra
DCAF7 P61962 ATN1 Homo sapiens Q86V38 32814053
Intra
DCAF7 P61962 ATN1 Homo sapiens Q86V38 32814053
Intra
DCAF7 P61962 LAMP2 Homo sapiens P13473-2 32814053
Intra
DCAF7 P61962 LAMP2 Homo sapiens P13473-2 32814053
Intra
DCAF7 P61962 LAMP2 Homo sapiens P13473-2 32814053
Intra
DCAF7 P61962 KLK6 Homo sapiens Q92876 32814053
Intra
DCAF7 P61962 KLK6 Homo sapiens Q92876 32814053
Intra
DCAF7 P61962 KLK6 Homo sapiens Q92876 32814053
Intra
DCAF7 P61962 HIPK2 Homo sapiens Q9H2X6 20940704
Intra
DCAF7 P61962 HIPK2 Homo sapiens Q9H2X6 33961781
Intra
DCAF7 P61962 HIPK2 Homo sapiens Q9H2X6
IF
20940704
Intra
DCAF7 P61962 TARDBP Homo sapiens Q13148 32814053
Intra
DCAF7 P61962 TARDBP Homo sapiens Q13148 32814053
Intra
DCAF7 P61962 TARDBP Homo sapiens Q13148 32814053
Intra
DCAF7 P61962 MAP3K1 Homo sapiens Q13233
IF
20940704
Intra
DCAF7 P61962 DYRK1B Homo sapiens Q9Y463
TAP
27705803
Intra
DCAF7 P61962 DYRK1B Homo sapiens Q9Y463 35016035
Intra
DCAF7 P61962 DYRK1B Homo sapiens Q9Y463 20940704
Intra
DCAF7 P61962 DYRK1B Homo sapiens Q9Y463 33961781
Intra
DCAF7 P61962 CASP6 Homo sapiens P55212 32814053
Intra
DCAF7 P61962 CASP6 Homo sapiens P55212 32814053
Intra
DCAF7 P61962 CASP6 Homo sapiens P55212 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
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

Diseases Alias
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

Orthologs Information

Species Symbol Source 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