Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
81605
Gene name Gene Name - the full gene name approved by the HGNC.
Ubiquitin related modifier 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
URM1
Synonyms (NCBI Gene) Gene synonyms aliases
C9orf74
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q34.11
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT028530 hsa-miR-30a-5p Proteomics 18668040
MIRT030374 hsa-miR-24-3p Microarray 19748357
MIRT722207 hsa-miR-3714 HITS-CLIP 19536157
MIRT722206 hsa-miR-370-5p HITS-CLIP 19536157
MIRT722205 hsa-miR-3622a-3p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002098 Process TRNA wobble uridine modification IMP 19017811
GO:0005515 Function Protein binding IPI 19017811, 21209336
GO:0005634 Component Nucleus IBA 21873635
GO:0005829 Component Cytosol IC 19017811
GO:0005829 Component Cytosol TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612693 28378 ENSG00000167118
Protein
UniProt ID Q9BTM9
Protein name Ubiquitin-related modifier 1
Protein function Acts as a sulfur carrier required for 2-thiolation of mcm(5)S(2)U at tRNA wobble positions of cytosolic tRNA(Lys), tRNA(Glu) and tRNA(Gln). Serves as sulfur donor in tRNA 2-thiolation reaction by being thiocarboxylated (-COSH) at its C-terminus
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09138 Urm1 6 101 Urm1 (Ubiquitin related modifier) Domain
Sequence
Sequence length 101
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Sulfur relay system   tRNA modification in the nucleus and cytosol
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Gastric cancer Hereditary Diffuse Gastric Cancer rs137854571, rs63751108, rs34612342, rs121908383, rs121909144, rs121909775, rs121909219, rs121909223, rs63750871, rs80359530, rs121964873, rs121913530, rs606231203, rs121918505, rs587776802
View all (244 more)
21364753
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 36769280
Nasopharyngeal Carcinoma Associate 16308470