Gene Name	FRG1
Gene ID	2483
Gene Full Name	FSHD region gene 1
Gene Alias	FRG1A|FSG1
Transcripts	ENSG00000109536
Virus	MCV
Gene Type	protein-coding
HPA Location Info
Membrane Info	Disease related genes, Human disease related genes, Predicted intracellular proteins
Uniport_ID	Q14331
HGNC ID	HGNC:3954
OMIM ID	601278
Summary	This gene maps to a location 100 kb centromeric of the repeat units on chromosome 4q35 which are deleted in facioscapulohumeral muscular dystrophy (FSHD). It is evolutionarily conserved and has related sequences on multiple human chromosomes but DNA sequence analysis did not reveal any homology to known genes. In vivo studies demonstrate the encoded protein is localized to the nucleolus. [provided by RefSeq, Jul 2008]

Integration Table: if previous studies reported that target gene was altered by virus integration events, the overlap between VISs in this literature and Cistrome factors was listed in this section

DVID	Chromosome	HM	TFBS	CA	Sum of Overlapped Records	Detail
7000033	chr4	619	215	61	895	View

Data ID	Experiment type	Sample number	Platform
GSE118056	scRNA-seq	4	Illumina NovaSeq 6000 (Homo sapiens)
GSE117988	scRNA-seq	6	Illumina HiSeq 2500 (Homo sapiens)
GSE136867	scRNA-seq	2	Illumina NextSeq 500 (Homo sapiens)
GSE226438	scRNA-seq	11	Illumina NovaSeq 6000 (Homo sapiens)