2. Gene
  3. PAPOLG - poly(A) polymerase gamma Gene

PAPOLG - poly(A) polymerase gamma Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens
Gene ID: 64895 | Gene type: protein coding

About PAPOLG

Cytogenetic location: 2p16.1 Genomic coordinates (GRCh38): 2:60,756,268-60,802,086 (from NCBI)

This gene has 7 transcripts (splice variants), 217 orthologues and 2 paralogues. Ubiquitous expression in thyroid (RPKM 5.8), testis (RPKM 3.7) and 25 other tissues.

Summary

This gene encodes a member of the poly(A) polymerase family which catalyzes template-independent extension of the 3' end of a DNA/RNA strand. This Enzyme shares 60% identity to the well characterized poly(A) polymerase II (PAPII) at the amino acid level. These two enzymes have similar organization of structural and functional domains. This Enzyme is exclusively localized in the nucleus and exhibits both nonspecific and CPSF (cleavage and polyadenylation specificity factor)/AAUAAA-dependent polyadenylation activity. This gene is located on chromosome 2 in contrast to the PAPII gene, which is located on chromosome 14. [provided by RefSeq, Jul 2008]

PAPOLG Products(1)

mRNA Protein Name
NM_022894.4 NP_075045.2 poly(A) polymerase gamma

PAPOLG Protein Structure

PAP_central

PAP_central: Poly(A) polymerase central domain (16 - 363)

NTP_transf_2

NTP_transf_2: Nucleotidyltransferase domain (94 - 172)

PAP_RNA-bind

PAP_RNA-bind: Poly(A) polymerase predicted RNA binding domain (365 - 506)

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  • 736 a.a.
Protein Preferred Names Protein Names

poly(A) polymerase gamma

PAP-gamma

Related Diseases

Diseases Alias
Acute Cystitis

Urinary Tract Infection

Recurrent Urinary Tract Infection
Pyelitis
Chromosome 2p16.1-P15 Deletion Syndrome

2p15p16.1 Microdeletion Syndrome

2p15-P16.1 Microdeletion Syndrome

Del(2)(P15p16.1)

Monosomy 2p15p16.1

Monosomy 2p15-P16.1
Peroxisome Biogenesis Disorder 11a

PBD11A

Peroxisome Biogenesis Disorder Complementation Group 13

PBD-CG13

Cg13

Pbd-Cgh

Peroxisome Biogenesis Disorder Complementation Group H

Peroxisome Biogenesis Disorder, Type 11a

Peroxisome Biogenesis Disorder, Complementation Group 13
Acute Pyelonephritis

Apn - [Acute Pyelonephritis]
Bacteriuria
Urinary Tract Infection

Urinary Tract Infections

Uti

Urinary Tract Infection Nos

Uti - [Urinary Tract Infection]

Uti Nos - [Urinary Tract Infection Nos]

Urosepsis Nos

E Coli Uti

E Coli Urinary Tract Infection

Escherichia Coli Uti
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS10027 PAPOLG Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus PAPOLG MGD MGI:2442119
Rattus norvegicus PAPOLG RGD RGD:1310337
Canis familiaris PAPOLG VGNC VGNC:54531
Felis catus PAPOLG VGNC VGNC:81139
Macaca mulatta PAPOLG VGNC VGNC:106193