Gene Name	RBM10
Gene ID	8241
Gene Full Name	RNA binding motif protein 10
Gene Alias	DXS8237E|GPATC9|GPATCH9|MINAS-60|S1-1|TARPS|ZRANB5
Transcripts	ENSG00000182872
Virus	HTLV1
Gene Type	protein-coding
HPA Location Info	Nuclear speckles;
Membrane Info	Cancer-related genes, Disease related genes, Human disease related genes, Predicted intracellular proteins
Uniport_ID	P98175
HGNC ID	HGNC:9896
OMIM ID	300080
Summary	This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]

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
6003222	chrX	147	21	7	175	View
6008575	chrX	39	4	1	44	View

Data ID	Experiment type	Sample number	Platform
GSE189602	Methylation profiling (Array)	4	Infinium MethylationEPIC
C   GSE94732	Chip-seq	24	Illumina NextSeq 500 (Homo sapiens);illumina Genome Analyzer IIx (Homo sapiens)
GSE52244	Expression array	15	[HuEx-1_0-st] Affymetrix Human Exon 1.0 ST Array [probe set (exon) version]
GSE224047	RNA-seq	10	Illumina NextSeq 500 (Homo sapiens)
GSE168557	Expression array	6	Agilent-039494 SurePrint G3 Human GE v2 8x60K Microarray 039381 (Feature Number version)
GSE136189	Methylation profiling (Array)	40	Illumina HumanMethylation450 BeadChip (HumanMethylation450_15017482);Illumina Infinium HumanMethylation850 BeadChip

• Genome binding/occupancy profiling

When the gene can detect a peak in the dataset, a peak plot will be displayed.

> Dataset: GSE94732 - RBM10 peak across samples

Peak Plot