NP
Primary Info
Mutation
Mouse studies
DNA sequencing


mRNA IDs Primary Information
NM_000270.2 Gene Symbol PNP
Protein Name Nucleoside phosphorylase
Alternate Names MGC117396, MGC125915, MGC125916, NP, PRO1837, PUNP
Gene Locus 14q13.1

External links
IDR HPRD OMIM Entrez Gene NetPath Reactome PDB HGNC Ensembl Swiss-Prot RefDIC
11 01247 164050 4860 4860 1M73
1PF7
1PWY
1RCT
1RFG
1RR6
1RSZ
1RT9
1ULA
1ULB
1V2H
1V3Q
1V41
1V45
1YRY
2A0W
2A0X
2A0Y
2OC4
2OC9
2ON6
7892 ENSG00000198805 P00491 PNP

Disease name Characteristic / Associated features Category inheritance type
Purine nucleoside phosphorylase deficiency; PNP deficiency Failure to thrive; sinusitis; otitis media; cerebral vasculitis; atrophic tonsils; recurrent upper respiratory tract infections; recurrent lower respiratory tract infections; pneumonia; splenomegaly; urinary tract infections; spastic diplegia; tetraparesis; ataxia; tremor; motor retardation; hypertonia; muscular hypotonia; behavioral disturbances; mental retardation; cerebral vasculitis; autoimmune hemolytic anemia; idiopathic thrombocytopenia; autoimmune neutropenia; frequent bacterial, viral, and opportunistic infections; lymphopenia; small lymph nodes; aplasia/Hypoplasia of the thymus; marked depletion of lymphoid tissues; markedly depressed T lymphocyte proportion; markedly reduced T cell function; abnormal B cell function; defective antibody production; lymphoma; lymphosarcoma; reduced erythrocyte purine nucleoside phosphorylase activity; hypouricemia; hypouricosuria; high serum inosine levels; high serum guanosine levels; high urinary excretion of inosine, 2-deoxyinosine, guanosine, and 2-deoxyguanosine; normal B-cell count Combined T-cell and B-cell immunodeficiencies Autosomal recessive