Entity Details

Primary name PAPSS2
Entity type gene
Source Source Link

Details

PrimaryID9060
RefseqGeneNG_012150
SymbolPAPSS2
Name3'-phosphoadenosine 5'-phosphosulfate synthase 2
Chromosome10
Location10q23.2-q23.31
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-01-14
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsPAPS2_HUMAN

GO terms

Show/Hide Table
GOName
GO:0000103 sulfate assimilation
GO:0001501 skeletal system development
GO:0004020 adenylylsulfate kinase activity
GO:0004781 sulfate adenylyltransferase (ATP) activity
GO:0005524 ATP binding
GO:0005829 cytosol
GO:0016779 nucleotidyltransferase activity
GO:0050428 3'-phosphoadenosine 5'-phosphosulfate biosynthetic process

Diseases

Show/Hide Table
Disease IDSourceNameDescription
612847 OMIMBrachyolmia type 4 with mild epiphyseal and metaphyseal changes (BCYM4)A form of brachyolmia, a clinically and genetically heterogeneous skeletal dysplasia primarily affecting the spine and characterized by a short trunk, short stature, and platyspondyly. BCYM4 is an autosomal recessive form with mild epiphyseal and metaphyseal changes. Clinical features include short stature evidenced at birth, short and bowed lower limbs, mild brachydactyly, kyphoscoliosis, abnormal gait, enlarged knee joints. Some BCYM4 patients may manifest premature pubarche and hyperandrogenism associated with skeletal dysplasia and short stature. The disease is caused by variants affecting the gene represented in this entry.