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USB1 encodes a protein with several conserved domains, however, its exact function is not known. Additionally we are shipping U6 SnRNA Biogenesis 1 Proteins (5) and many more products for this protein.
Showing 10 out of 38 products:
Human Polyclonal USB1 Primary Antibody for ELISA, WB - ABIN4320731
Walne, Vulliamy, Beswick, Kirwan, Dokal: Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndrome. in Human molecular genetics 2010
marked overlap of dyskeratosis congenita with four other genetic syndromes, confounding accurate diagnosis and subsequent management. Patients with clinical features of dyskeratosis congenita need to have genetic analysis of USB1, LIG4 (show LIG4 Antibodies) and GRHL2 (show GRHL2 Antibodies) in addition to the classical dyskeratosis congenita genes and telomere length measurements.
USB1 genes from myelodysplastic and myelodysplastic/myeloproliferative neoplasms and AML (show RUNX1 Antibodies) had 3 unreported variants, 2 in USB1 5'UTR (show UTS2R Antibodies) (c.-83G>T and c.-66A>G), 1 in IVS3 (c.450-68dupT) and 1 (<1%) in IVS4 (c.587+21A>G/rs200924980) were detected.
the link between Mpn1 and snRNA stability
Mpn1 associates with the NineTeen Complex, a multiprotein complex that is essential for the maintenance of spliceosome integrity and efficient splicing. [Review]
Data indicate that USB1 measures the appropriate length of the U6 oligo(U) tail by reading the position of a key adenine nucleotide (A102) and pausing 5 uridine residues downstream.
Recombinant hMpn1 is a 3'-to-5' RNA exonuclease (show EXO1 Antibodies) that removes uridines from U6 3' ends, generating terminal 2',3' cyclic phosphates in vitro.
characterization of 6 Poikiloderma with Neutropenia patients and mutational repertoire of the gene; detected 2 novel C16orf57 mutations, c.232C>T and c.265 2T>G and the reported c.179delC, c.531delA and c.693 1G>T mutations; bioinformatic prediction of the C16orf57 protein structure denotes a very basic enzymatic function consistent with a housekeeping function
We report three cases of poikiloderma with neutropenia whose clinical presentations, laboratory investigations, and C16orf57 mutation support the diagnosis.
Advanced bioinformatics predicted that C16orf57 encodes a phosphodiesterase whose putative catalytic activity is essential for its function in vivo
Mutations of the C16orf57 gene permit the unification of a distinct group of genetic polikilodermal dermatoses that can be diagnosed as congenital dyskeratosis, Rothmund-Thomson syndrome, poikiloderma-neutropenia.
This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.
HVSL motif containing 1
, U six biogenesis 1
, U6 snRNA phosphodiesterase
, UPF0406 protein C16orf57
, mutated in poikiloderma with neutropenia protein 1
, putative U6 snRNA phosphodiesterase
, UPF0406 protein C16orf57 homolog