Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
26122
Gene name Gene Name - the full gene name approved by the HGNC.
Enhancer of polycomb 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
EPC2
Synonyms (NCBI Gene) Gene synonyms aliases
EPC-LIKE
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q23.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT085668 hsa-miR-194-5p PAR-CLIP 21572407
MIRT085676 hsa-miR-5692a PAR-CLIP 21572407
MIRT085671 hsa-miR-802 PAR-CLIP 21572407
MIRT085677 hsa-miR-5692b PAR-CLIP 21572407
MIRT085675 hsa-miR-5692c PAR-CLIP 21572407
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000786 Component Nucleosome IDA 27153538
GO:0005634 Component Nucleus IEA
GO:0006281 Process DNA repair IEA
GO:0006325 Process Chromatin organization IEA
GO:0006357 Process Regulation of transcription by RNA polymerase II IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611000 24543 ENSG00000135999
Protein
UniProt ID Q52LR7
Protein name Enhancer of polycomb homolog 2 (EPC-like)
Protein function May play a role in transcription or DNA repair.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10513 EPL1 7 149 Enhancer of polycomb-like Family
PF06752 E_Pc_C 577 807 Enhancer of Polycomb C-terminus Family
Sequence
MSKLSFRARALDAAKPLPIYRGKDMPDLNDCVSINRAVPQMPTGMEKEEESEHHLQRAIS
AQQVFREKKESMVIPVPEAESNVNYYNRLYKGEFKQPKQFIHIQPFNLDNEQPDYDMDSE
DETLLNRLNRKMEIKPLQFEIMIDRLEKA
SSNQLVTLQEAKLLLNEDDYLIKAVYDYWVR
KRKNCRGPSLIPQIKQEKRDGSTNNDPYVAFRRRTEKMQTRKNRKNDEASYEKMLKLRRE
FSRAITILEMIKRREKTKRELLHLTLEVVEKRYHLGDYGGEILNEVKISRSEKELYATPA
TLHNGNHHKVQECKTKHPHHLSLKEEASDVVRQKKKYPKKPKAEALITSQQPTPETLPVI
NKSDIKQYDFHSSDEDEFPQVLSPVSEPEEENDPDGPCAFRRRAGCQYYAPRLDQANHSC
ENSELADLDKLRYRHCLTTLTVPRRCIGFARRRIGRGGRVIMDRISTEHDPVLKQIDPEM
LNSFSSSSQTIDFSSNFSRTNASSKHCENRLSLSEILSNIRSCRLQCFQPRLLNLQDSDS
EECTSRKPGQTVNNKRVSAASVALLNTSKNGISVTGGITEEQFQTHQQQLVQMQRQQLAQ
LQQKQQSQHSSQQTHPKAQGSSTSDCMSKTLDSASAHFAASAVVSAPVPSRSEVAKEQNT
GHNNINGVVQPSGTSKTLYSTNMALSSSPGISAVQLVRTVGHTTTNHLIPALCTSSPQTL
PMNNSCLTNAVHLNNVSVVSPVNVHINTRTSAPSPTALKLATVAASMDRVPKVTPSSAIS
SIARENHEPERLGLNGIAETTVAMEVT
Sequence length 807
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  ATP-dependent chromatin remodeling  
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Diabetes Type 2 diabetes N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 21123754
Autistic Disorder Associate 22085900
Delayed Cranial Ossification due to CBFB Haploinsufficiency Associate 19904302
Heart Diseases Associate 30578870
Intellectual Disability Associate 19809484