Name

LOC100419991 Gene

phosphoserine phosphatase pseudogene

PSAT1P3 Gene

phosphoserine aminotransferase 1 pseudogene 3

PSAT1P1 Gene

phosphoserine aminotransferase 1 pseudogene 1

PSAT1P4 Gene

phosphoserine aminotransferase 1 pseudogene 4

PSAT1 Gene

phosphoserine aminotransferase 1

This gene encodes a member of the class-V pyridoxal-phosphate-dependent aminotransferase family. The encoded protein is a phosphoserine aminotransferase and decreased expression may be associated with schizophrenia. Mutations in this gene are also associated with phosphoserine aminotransferase deficiency. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene have been defined on chromosomes 1, 3, and 8. [provided by RefSeq, Jul 2013]

PSPHP1 Gene

phosphoserine phosphatase pseudogene 1

This gene is significantly upregulated in Fanconi's anemia fibroblasts but downregulated or absent in fibroblasts from normal donors. It is also highly expressed in FA B-cells of complementation group A. [provided by RefSeq, Jul 2008]

SEPSECS Gene

Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase

The amino acid selenocysteine is the only amino acid that does not have its own tRNA synthetase. Instead, this amino acid is synthesized on its cognate tRNA in a three step process. The protein encoded by this gene catalyzes the third step in the process, the conversion of O-phosphoseryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec).[provided by RefSeq, Mar 2011]

PSPH Gene

phosphoserine phosphatase

The protein encoded by this gene belongs to a subfamily of the phosphotransferases. This encoded enzyme is responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome. [provided by RefSeq, Jul 2008]

ARMT1 Gene

acidic residue methyltransferase 1

Enables S-adenosylmethionine-dependent methyltransferase activity; enzyme binding activity; and protein carboxyl O-methyltransferase activity. Involved in DNA damage response. [provided by Alliance of Genome Resources, Mar 2025]

UBA52 Gene

ubiquitin A-52 residue ribosomal protein fusion product 1

Ubiquitin is a highly conserved nuclear and cytoplasmic protein that has a major role in targeting cellular proteins for degradation by the 26S proteosome. It is also involved in the maintenance of chromatin structure, the regulation of gene expression, and the stress response. Ubiquitin is synthesized as a precursor protein consisting of either polyubiquitin chains or a single ubiquitin moiety fused to an unrelated protein. This gene encodes a fusion protein consisting of ubiquitin at the N terminus and ribosomal protein L40 at the C terminus, a C-terminal extension protein (CEP). Multiple processed pseudogenes derived from this gene are present in the genome. [provided by RefSeq, Jul 2008]

LOC100289117 Gene

ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene

UBA52P8 Gene

ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 8

UBA52P9 Gene

ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 9

UBA52P1 Gene

ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 1

UBA52P2 Gene

ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 2

UBA52P3 Gene

ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 3

UBA52P4 Gene

ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 4

UBA52P6 Gene

ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 6

UBA52P7 Gene

ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 7

UBA52P5 Gene

ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 5

NARR Gene

nine-amino acid residue-repeats