Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
7324
Gene name Gene Name - the full gene name approved by the HGNC.
Ubiquitin conjugating enzyme E2 E1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
UBE2E1
Synonyms (NCBI Gene) Gene synonyms aliases
UBCH6
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p24.2
Summary Summary of gene provided in NCBI Entrez Gene.
The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, or E1s, ubiquitin-conju
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029169 hsa-miR-26b-5p Microarray 19088304
MIRT091614 hsa-miR-5692a PAR-CLIP 21572407
MIRT091615 hsa-miR-6507-5p PAR-CLIP 21572407
MIRT091614 hsa-miR-5692a PAR-CLIP 21572407
MIRT091615 hsa-miR-6507-5p 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:0000151 Component Ubiquitin ligase complex IDA 15247280, 16307923
GO:0000209 Process Protein polyubiquitination IBA 21873635
GO:0000209 Process Protein polyubiquitination IDA 15247280, 16522193
GO:0004842 Function Ubiquitin-protein transferase activity IDA 16307923, 16522193, 20061386
GO:0005515 Function Protein binding IPI 16307923, 19549727, 19690564, 24446487, 26752685, 28514442
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602916 12477 ENSG00000170142
Protein
UniProt ID P51965
Protein name Ubiquitin-conjugating enzyme E2 E1 (EC 2.3.2.23) ((E3-independent) E2 ubiquitin-conjugating enzyme E1) (EC 2.3.2.24) (E2 ubiquitin-conjugating enzyme E1) (UbcH6) (Ubiquitin carrier protein E1) (Ubiquitin-protein ligase E1)
Protein function Accepts ubiquitin from the E1 complex and catalyzes its covalent attachment to other proteins. Catalyzes the covalent attachment of ISG15 to other proteins. Mediates the selective degradation of short-lived and abnormal proteins. In vitro also c
PDB 1XR9 , 3BZH , 4JJQ , 5LBN , 6FGA , 8IYA
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00179 UQ_con 51 188 Ubiquitin-conjugating enzyme Domain
Sequence
Sequence length 193
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Ubiquitin mediated proteolysis   ISG15 antiviral mechanism
Inactivation of APC/C via direct inhibition of the APC/C complex
APC/C:Cdc20 mediated degradation of Cyclin B
Autodegradation of Cdh1 by Cdh1:APC/C
APC/C:Cdc20 mediated degradation of Securin
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1
Cdc20:Phospho-APC/C mediated degradation of Cyclin A
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase
Regulation of APC/C activators between G1/S and early anaphase
APC/C:Cdc20 mediated degradation of mitotic proteins
Phosphorylation of the APC/C
APC-Cdc20 mediated degradation of Nek2A
Separation of Sister Chromatids
Senescence-Associated Secretory Phenotype (SASP)
CDK-mediated phosphorylation and removal of Cdc6
Transcriptional Regulation by VENTX
Synthesis of active ubiquitin: roles of E1 and E2 enzymes
E3 ubiquitin ligases ubiquitinate target proteins
Antigen processing: Ubiquitination & Proteasome degradation
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
Unknown
Disease term Disease name Evidence References Source
Lung adenocarcinoma Lung adenocarcinoma Validation that loss of Tgfbr2 results in more aggressive and T cell-excluded KP lung tumors GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Frontotemporal Dementia Associate 25580532
Leukemia Myeloid Acute Associate 27855695
Leukemia Promyelocytic Acute Associate 27855695
Moyamoya Disease Associate 40722175
Polycystic Ovary Syndrome Associate 34477128
Retinal Degeneration Associate 21139979
Retinoblastoma Associate 34347012