Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
139105
Gene name Gene Name - the full gene name approved by the HGNC.
BEN domain containing 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
BEND2
Synonyms (NCBI Gene) Gene synonyms aliases
CXorf20
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xp22.13
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein which has two BEN domains in the C-terminus. These domains are found in proteins which participate in protein and DNA interactions which occur during chromatin restructuring or transcription. Alternative splicing results in mul
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT820688 hsa-miR-1225-3p CLIP-seq
MIRT820689 hsa-miR-1233 CLIP-seq
MIRT820690 hsa-miR-1254 CLIP-seq
MIRT820691 hsa-miR-3064-3p CLIP-seq
MIRT820692 hsa-miR-3116 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
301150 28509 ENSG00000177324
Protein
UniProt ID Q8NDZ0
Protein name BEN domain-containing protein 2
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10523 BEN 504 577 BEN domain Domain
PF10523 BEN 689 762 BEN domain Domain
Sequence
MSERTQEQDFVIITVDDSDDNNDCSIEMVEVSETADNSTNDIADDSTYVTADNPTDDTAT
QPNFPGGNDGHHRPLQMSYGSGSVTQAGVQWHDHSSLQPQPLGLKQFFHLSLPSSWDDRR
TPPCPVAHGDQIVSQINHPVHLRRYSYNSEEVDFPKRGRFYTPEVQSSISPPAERQETHA
WASPAVTSLESAACHELQEADLSESLSYPRIVSSSSLQQYVAQGGSFPCFGMPWNFISGG
AESTNAVISFANATTAVPMAVLSRRESSLANNPGVVNYSALPENENVGPGRALSSFCFHP
NLEMPERPANSSKNSTETANYPTLMGNYNGQNTASLSVFIPPYFAEKIILTEMPGTTETN
VENNSQTVYYPALSGNTSAPYPASSYLPITSNFESGPQMSYGTMSYSTEMKNNCDQDDAS
ASACLTPDFALLPLNILVKVDTNTENSVNTMNRSTLLDSDSGQDSSSSSVCIPPKYGYLG
DPKRNVRVLKIHLLAVQNMAKPKQAACYLVRILFSKEILISSSVDIHLKDSQSLDPNKMA
ALREYLATTFPTCDLHEHGKDWQDCISGINSMIYCLC
SEGKSTPKTVRKNKKRTNRVASA
SADRNDQRGRDGGEGCSWMFQPMNNSKMREKRNLQPNSNAIPEGMREPSTDNPEEPGEAW
SYFGRPWRNIRMPCSVLTLAKTKSCASLSARYLIQKLFTKDVLVQSNVYGNLKHGLCALD
PNKISALREFLQENYPICDLSENGRDWKSCVTSINSGIRSLR
HDVRRAEARSQSLPAVTP
PELEQESKPGDPDATDPST
Sequence length 799
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Arthritis Juvenile arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 19565504
Associations from Text Mining
Disease Name Relationship Type References
Azoospermia Nonobstructive Associate 36017582
Central Nervous System Infections Associate 29348602
Cushing Syndrome Associate 36690805
Glioblastoma Associate 35757013
Glioma Associate 39529180
Gliosarcoma Associate 35757013
Neoplasms Associate 31160355, 35440587
Neoplasms Neuroepithelial Associate 29348602, 39529180
Pancreatic Neoplasms Associate 32124419, 36690805