Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
65992
Gene name Gene Name - the full gene name approved by the HGNC.
DDRGK domain containing 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DDRGK1
Synonyms (NCBI Gene) Gene synonyms aliases
C20orf116, SEMDSH, UFBP1, dJ1187M17.3
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20p13
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene interacts with components of the ubiquitin fold modifier 1 conjugation pathway and helps prevent apoptosis in ER-stressed secretory tissues. In addition, the encoded protein regulates nuclear factor-κB activity. [prov
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1325869434 C>T Pathogenic Splice donor variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020874 hsa-miR-155-5p Proteomics 18668040
MIRT049458 hsa-miR-92a-3p CLASH 23622248
MIRT929564 hsa-miR-1246 CLIP-seq
MIRT929565 hsa-miR-4320 CLIP-seq
MIRT929566 hsa-miR-4635 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 20018847, 20228063, 23675531, 25219498, 28128204, 28263186, 32160526, 33961781, 35156780, 36012204, 37595036
GO:0005730 Component Nucleolus IDA
GO:0005737 Component Cytoplasm TAS 23675531
GO:0005783 Component Endoplasmic reticulum IDA 20018847
GO:0005783 Component Endoplasmic reticulum IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616177 16110 ENSG00000198171
Protein
UniProt ID Q96HY6
Protein name DDRGK domain-containing protein 1 (Dashurin) (UFM1-binding and PCI domain-containing protein 1)
Protein function Component of the UFM1 ribosome E3 ligase (UREL) complex, a multiprotein complex that catalyzes ufmylation of endoplasmic reticulum-docked proteins (PubMed:30626644, PubMed:32160526, PubMed:35753586, PubMed:36121123, PubMed:36543799, PubMed:37595
PDB 7W3N , 8B9X , 8C0D , 8OHD , 8OJ0 , 8OJ5
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09756 DDRGK 115 303 DDRGK domain Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed (at protein level). In the brain, highest levels in medulla oblongata, followed by cerebral cortex, cerebellum and frontal lobe. {ECO:0000269|PubMed:20018847, ECO:0000269|PubMed:20036718}.
Sequence
MVAPVWYLVAAALLVGFILFLTRSRGRAASAGQEPLHNEELAGAGRVAQPGPLEPEEPRA
GGRPRRRRDLGSRLQAQRRAQRVAWAEADENEEEAVILAQEEEGVEKPAETHLSGKIGAK
KLRKLEEKQARKAQREAEEAEREERKRLESQREAEWKKEEERLRLEEEQKEEEERKAREE
QAQREHEEYLKLKEAFVVEEEGVGETMTEEQSQSFLTEFINYIKQSKVVLLEDLASQVGL
RTQDTINRIQDLLAEGTITGVIDDRGKFIYITPEELAAVANFIRQRGRVSIAELAQASNS
LIA
WGRESPAQAPA
Sequence length 314
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Spondyloepimetaphyseal dysplasia spondyloepimetaphyseal dysplasia, shohat type rs1325869434 N/A
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
Parkinson Disease Parkinson's disease N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 35680375
Neoplasms Associate 30228783, 36965071
Osteosarcoma Associate 36965071
Stomach Neoplasms Inhibit 30228783