Gene table of RBMX : RNA binding motif protein, X-linked

Gene-disease associations table

Disease ID	Disease name	Source of annotation with RBMX	OMIM link	Number of associated genes	genes
PS309510	MENTAL RETARDATION, X-LINKED SYNDROMIC	OMIM	link to OMIM	27	AP1S2, PRPS1, IGBP1, RBMX, HUWE1, RAB40AL, HSD17B10, ATP6AP2, PHF8, CLIC2, CASK, TAF1, FGD1, CUL4B, PQBP1, ZDHHC9, NONO, UPF3B, SMS, HDAC8, UBE2A, MECP2, KDM5C, ARX, SLC9A6, GRIA3, PHF6

Associated genes in ENSEMBL

Associated proteins - SwissProt Accession ID

Associated PDB IDs

Cytogenetic Band

Tandem repeats annotation

Transcription regulation as annotated in TRRUST

Associated KEGG pathways

KEGG pathway	KEGG ID	KEGG IC
Spliceosome	hsa03040	5.73

Associated REACTOME pathways

REACTOME pathway	REACTOME ID	REACTOME IC
Gene Expression	R-HSA-74160	2.72
mRNA Splicing - Major Pathway	R-HSA-72163	6.15
Processing of Capped Intron-Containing Pre-mRNA	R-HSA-72203	6.1
mRNA Splicing	R-HSA-72172	6.15

Associated GO terms for Molecular function

GO term	GO ID	GO IC
transcription regulatory region DNA binding	GO:0044212	3.03
protein binding	GO:0005515	0.46
organic cyclic compound binding	GO:0097159	1.05
poly(A) RNA binding	GO:0044822	2.69
regulatory region DNA binding	GO:0000975	3.03
regulatory region nucleic acid binding	GO:0001067	3.03
nucleotide binding	GO:0000166	1.96
small molecule binding	GO:0036094	1.89
macromolecular complex binding	GO:0044877	2.61
binding	GO:0005488	0.18
nucleic acid binding	GO:0003676	1.44
DNA binding	GO:0003677	1.92
core promoter binding	GO:0001047	4.71
RNA binding	GO:0003723	2.36
chromatin binding	GO:0003682	3.64
heterocyclic compound binding	GO:1901363	1.06
nucleoside phosphate binding	GO:1901265	1.96
mRNA binding	GO:0003729	4.68