Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
80700
Gene name Gene Name - the full gene name approved by the HGNC.
UBX domain protein 6
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
UBXN6
Synonyms (NCBI Gene) Gene synonyms aliases
UBXD1, UBXDC2
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT045110 hsa-miR-186-5p CLASH 23622248
MIRT040969 hsa-miR-18a-3p CLASH 23622248
MIRT1472193 hsa-miR-1286 CLIP-seq
MIRT1472194 hsa-miR-324-5p CLIP-seq
MIRT1472195 hsa-miR-338-3p 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 18656546, 18775313, 19275885, 21822278, 22337587, 23349634, 25416956, 27753622, 29892012, 29997244, 31515488, 32296183, 32814053, 33961781, 35271311, 37776851
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IDA 27753622
GO:0005737 Component Cytoplasm IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611946 14928 ENSG00000167671
Protein
UniProt ID Q9BZV1
Protein name UBX domain-containing protein 6 (UBX domain-containing protein 1)
Protein function May negatively regulate the ATPase activity of VCP, an ATP-driven segregase that associates with different cofactors to control a wide variety of cellular processes (PubMed:26475856). As a cofactor of VCP, it may play a role in the transport of
PDB 6SAP , 8FCL , 8FCM , 8FCN , 8FCO , 8FCP , 8FCQ , 8FCR , 8FCT
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09409 PUB 168 255 PUB domain Domain
PF00789 UBX 332 410 UBX domain Domain
Tissue specificity TISSUE SPECIFICITY: Enhanced expression in testis.
Sequence
MKKFFQEFKADIKFKSAGPGQKLKESVGEKAHKEKPNQPAPRPPRQGPTNEAQMAAAAAL
ARLEQKQSRAWGPTSQDTIRNQVRKELQAEATVSGSPEAPGTNVVSEPREEGSAHLAVPG
VYFTCPLTGATLRKDQRDACIKEAILLHFSTDPVAASIMKIYTFNKDQDRVKLGVDTIAK
YLDNIHLHPEEEKYRKIKLQNKVFQERINCLEGTHEFFEAIGFQKVLLPAQDQEDPEEFY
VLSETTLAQPQSLER
HKEQLLAAEPVRAKLDRQRRVFQPSPLASQFELPGDFFNLTAEEI
KREQRLRSEAVERLSVLRTKAMREKEEQRGLRKYNYTLLRVRLPDGCLLQGTFYARERLG
AVYGFVREALQSDWLPFELLASGGQKLSEDENLALNECGLVPSALLTFSW
DMAVLEDIKA
AGAEPDSILKPELLSAIEKLL
Sequence length 441
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Protein processing in endoplasmic reticulum  
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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
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Multiple Sclerosis Multiple sclerosis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Amyotrophic Lateral Sclerosis Associate 26475856
Frontotemporal Dementia Associate 26475856