Gene Name	NCL
Gene ID	4691
Gene Full Name	nucleolin
Gene Alias	C23|Nsr1
Transcripts	ENSG00000115053
Virus	HBV
Gene Type	protein-coding
HPA Location Info	Nucleoplasm, Nucleoli, Nucleoli rim;Mitotic chromosome;
Membrane Info	Plasma proteins, Predicted intracellular proteins
Uniport_ID	P19338
HGNC ID	HGNC:7667
OMIM ID	164035
Summary	Nucleolin (NCL), a eukaryotic nucleolar phosphoprotein, is involved in the synthesis and maturation of ribosomes. It is located mainly in dense fibrillar regions of the nucleolus. Human NCL gene consists of 14 exons with 13 introns and spans approximately 11kb. The intron 11 of the NCL gene encodes a small nucleolar RNA, termed U20. [provided by RefSeq, Jul 2008]

Mutation Table: if previous studies reported that target gene was related to virus gene/region/protein, the information in this literature was listed in this section

ID	PMID	Mutation	Gene/Protein/Region	Encoding Gene/Protein	Disease	Description	Detail
1	15564475	I97E	C	C	Hepatitis B Virus Infection	T	View
2	15564475	I97W	C	C	Hepatitis B Virus Infection	T	View
3	15564475	I97D	C	C	Hepatitis B Virus Infection	T	View
4	15564475	I97G	C	C	Hepatitis B Virus Infection	T	View
5	15564475	I97P	C	C	Hepatitis B Virus Infection	T	View
6	15564475	I97L	C	C	Hepatitis B Virus Infection	T	View
7	15564475	I97A	C	C	Hepatitis B Virus Infection	T	View
8	15564475	I97C	C	C	Hepatitis B Virus Infection	T	View
9	15564475	I97F	C	C	Hepatitis B Virus Infection	T	View
10	15564475	I97V	C	C	Hepatitis B Virus Infection	T	View
11	15564475	I97Y	C	C	Hepatitis B Virus Infection	T	View

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
1020958	chr2	16	4	0	20	View

Data ID	Experiment type	Sample number	Platform
GSE252863	scRNA-seq	10	Illumina HiSeq 2500 (Homo sapiens)
GSE236281	RNA-seq	12	Illumina MiSeq (Homo sapiens)
C   GSE35465	Chip-seq;RNA-seq	6	Illumina HiSeq 2000 (Homo sapiens)
GSE199850	scRNA-seq	1	HiSeq X Ten (Homo sapiens)
C   GSE68402	Chip-seq	26	Illumina MiSeq (Homo sapiens);Illumina HiSeq 2500 (Homo sapiens)
S   GSE247322	scRNA-seq	27	Illumina NovaSeq 6000 (Homo sapiens)
TCGA_LIHC_HBV	DNA methylation sequencing;RNA-seq	97	TCGA
C   GSE270130	Chip-seq	27	Illumina NovaSeq 6000 (Homo sapiens)
GSE224901	RNA-seq	21	Illumina NovaSeq 6000 (Homo sapiens)
GSE100400	Chip-seq;RNA-seq;4C_cccDNA	31	Illumina NextSeq 500 (Homo sapiens);Illumina NextSeq 500 (Mus musculus)
GSE173897	RNA-seq	95	Illumina HiSeq 4000 (Homo sapiens)
GSE262515	RNA-seq	21	Illumina HiSeq 2500 (Homo sapiens);Illumina HiSeq 2500 (Mus musculus)
GSE110345	RNA-seq	4	Illumina HiSeq 2500 (Homo sapiens)
C   GSE131257	ATAC-seq;RNA-seq	19	Illumina HiSeq 2500 (Homo sapiens)
GSE94660	RNA-seq	42	Illumina HiSeq 2500 (Homo sapiens)

• scRNA data
• Genome binding/occupancy profiling

When the query gene is differentially changed in the dataset, a feature/violin plot will be displayed.

> Dataset: GSE247322 - Gene expression in cell subsets