Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
56271
Gene name Gene Name - the full gene name approved by the HGNC.
Brain expressed X-linked 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
BEX4
Synonyms (NCBI Gene) Gene synonyms aliases
BEXL1
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xq22.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is a member of the brain expressed X-linked gene family. The proteins encoded by some of the other members of this family act as transcription elongation factors which allow RNA polymerase II to escape pausing during elongation. Multiple alterna
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT016667 hsa-miR-425-5p Sequencing 20371350
MIRT040055 hsa-miR-615-3p CLASH 23622248
MIRT645681 hsa-miR-8485 HITS-CLIP 23824327
MIRT645680 hsa-miR-329-3p HITS-CLIP 23824327
MIRT645679 hsa-miR-362-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000922 Component Spindle pole IDA 27512957
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IBA 21873635
GO:0005634 Component Nucleus IDA 27512957
GO:0005654 Component Nucleoplasm IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
300692 25475 ENSG00000102409
Protein
UniProt ID Q9NWD9
Protein name Protein BEX4 (BEX1-like protein 1) (Brain-expressed X-linked protein 4) (Nerve growth factor receptor-associated protein 3)
Protein function May play a role in microtubule deacetylation by negatively regulating the SIRT2 deacetylase activity toward alpha-tubulin and thereby participate in the control of cell cycle progression and genomic stability (PubMed:27512957). In absence of red
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04538 BEX 14 116 Brain expressed X-linked like family Family
Tissue specificity TISSUE SPECIFICITY: Very high expression in heart, skeletal muscle, liver, and kidney. The levels of expression are uniform throughout the brain. {ECO:0000269|PubMed:15958283}.
Sequence
Sequence length 120
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cholestasis Cholestasis rs121909103, rs751511532, rs376368459, rs762702807, rs1578490102, rs1578499691, rs1578504946, rs1317656688, rs199791850, rs1452792080, rs1578491039 27989131
Associations from Text Mining
Disease Name Relationship Type References
Aneuploidy Associate 39735979
Colorectal Neoplasms Associate 31796117
Neoplasms Associate 39735979
Stomach Neoplasms Associate 33217815
Thymoma Associate 39735979