Gene Gene information from NCBI Gene database.
Entrez ID 56943
Gene name ENY2 transcription and export complex 2 subunit
Gene symbol ENY2
Synonyms (NCBI Gene)
DC6Sus1e(y)2
Chromosome 8
Chromosome location 8q23.1
miRNA miRNA information provided by mirtarbase database.
122
miRTarBase ID miRNA Experiments Reference
MIRT031484 hsa-miR-16-5p Proteomics 18668040
MIRT964940 hsa-miR-1207-3p CLIP-seq
MIRT964941 hsa-miR-1272 CLIP-seq
MIRT964942 hsa-miR-146a CLIP-seq
MIRT964943 hsa-miR-146b-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
36
GO ID Ontology Definition Evidence Reference
GO:0000124 Component SAGA complex IBA
GO:0000124 Component SAGA complex IDA 18206972, 23591820, 27601583
GO:0000124 Component SAGA complex IEA
GO:0000124 Component SAGA complex NAS 19114550
GO:0003682 Function Chromatin binding IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619015 24449 ENSG00000120533
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NPA8
Protein name Transcription and mRNA export factor ENY2 (Enhancer of yellow 2 transcription factor homolog)
Protein function Involved in mRNA export coupled transcription activation by association with both the TREX-2 and the SAGA complexes. The transcription regulatory histone acetylation (HAT) complex SAGA is a multiprotein complex that activates transcription by re
PDB 4DHX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10163 EnY2 13 95 Transcription factor e(y)2 Family
Sequence
Sequence length 101
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
MULTIPLE SYSTEM ATROPHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Breast Carcinoma Breast Carcinoma BEFREE 22961600
★☆☆☆☆
Found in Text Mining only
Diabetes Diabetes BEFREE 23057668
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Diabetes Mellitus BEFREE 23057668
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of breast Breast Cancer BEFREE 22961600
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 27132940
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 27132940
★☆☆☆☆
Found in Text Mining only
Triple Negative Breast Neoplasms Triple Negative Breast Neoplasms BEFREE 30977117
★☆☆☆☆
Found in Text Mining only