Entity Details

Primary name PSPH
Entity type gene
Source Source Link

Details

PrimaryID5723
RefseqGeneNG_011473
SymbolPSPH
Namephosphoserine phosphatase
Chromosome7
Location7p11.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1989-04-24
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSERB_HUMAN

GO terms

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GOName
GO:0000287 magnesium ion binding
GO:0001701 in utero embryonic development
GO:0004647 phosphoserine phosphatase activity
GO:0005737 cytoplasm
GO:0005829 cytosol
GO:0006563 L-serine metabolic process
GO:0006564 L-serine biosynthetic process
GO:0009612 response to mechanical stimulus
GO:0016311 dephosphorylation
GO:0031667 response to nutrient levels
GO:0033574 response to testosterone
GO:0036424 L-phosphoserine phosphatase activity
GO:0036425 D-phosphoserine phosphatase activity
GO:0042802 identical protein binding
GO:0042803 protein homodimerization activity
GO:0043005 neuron projection

Diseases

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Disease IDSourceNameDescription
614023 OMIMPhosphoserine phosphatase deficiency (PSPHD)An autosomal recessive disorder that results in pre- and postnatal growth retardation, moderate psychomotor retardation and facial features suggestive of Williams syndrome. The disease is caused by variants affecting the gene represented in this entry.