1. Gene
  2. GNL3 - G protein nucleolar 3 Gene

GNL3 - G protein nucleolar 3 Gene

Homo sapiens

Also known as NS; E2IG3; NNP47; C77032

Gene ID: 26354 | Gene type: protein coding

About GNL3

Cytogenetic location: 3p21.1 Genomic coordinates (GRCh38): 3:52,685,920-52,694,497 (from NCBI)

This gene has 12 transcripts (splice variants), 203 orthologues and 6 paralogues. Ubiquitous expression in urinary bladder (RPKM 35.8), prostate (RPKM 32.9) and 25 other tissues.

Summary

The protein encoded by this gene may interact with p53 and may be involved in tumorigenesis. The encoded protein also appears to be important for stem cell proliferation. This protein is found in both the nucleus and nucleolus. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Nov 2010]

GNL3 Products(3)

mRNA Protein Name
NM_014366.5 NP_055181.3 guanine nucleotide-binding protein-like 3 isoform 1
NM_206825.2 NP_996561.1 guanine nucleotide-binding protein-like 3 isoform 2
NM_206826.1 NP_996562.1 guanine nucleotide-binding protein-like 3 isoform 2
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables mRNA 5'-UTR binding IDA
IDA: Inferred from direct assay
16213212 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16097049 GOA
Biological Process GO Annotation Evidence Reference Source
involved in positive regulation of miRNA transcription IMP
IMP: Inferred from mutant phenotype
25569094 GOA
involved in positive regulation of protein localization to chromosome, telomeric region IMP
IMP: Inferred from mutant phenotype
22641345 GOA
involved in positive regulation of protein sumoylation IMP
IMP: Inferred from mutant phenotype
22641345 GOA
involved in positive regulation of telomere maintenance IMP
IMP: Inferred from mutant phenotype
22641345 GOA
involved in stem cell division IDA
IDA: Inferred from direct assay
25522312 GOA
involved in stem cell population maintenance IMP
IMP: Inferred from mutant phenotype
25522312 GOA
Cellular Component GO Annotation Evidence Reference Source
located in nucleolus IDA
IDA: Inferred from direct assay
22641345 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

GNL3 Protein Structure

GN3L_Grn1

GN3L_Grn1: GNL3L/Grn1 putative GTPase (16 - 91)

MMR_HSR1

MMR_HSR1: 50S ribosome-binding GTPase (256 - 314)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 549 a.a.
Protein Preferred Names Protein Names

guanine nucleotide-binding protein-like 3

E2-induced gene 3 protein

Related Diseases

Diseases Alias
Tibial Adamantinoma

Tibial Adamantinoma Morphology

Diamond-Blackfan Anemia

Congenital Pure Red Cell Aplasia

Aase Syndrome

Erythrogenesis Imperfecta

Anemia, Diamond-Blackfan

Congenital Hypoplastic Anemia

Aase-Smith Ii Syndrome

Bds

Blackfan-Diamond Anemia

Congenital Prca

Congenital Hypoplastic Anemia, Blackfan-Diamond Type

Dba

Blackfan - Diamond Syndrome

Chronic Constitutional Pure Red Cell Anaemia

Anemia Diamond Blackfan Type

Anemia Congenital Erythroid Hypoplastic

Aregenerative Anemia Chronic Congenital

Blackfan Diamond Syndrome

Red Cell Aplasia, Pure Hereditary

Aase-Smith Syndrome Ii

Bda

Blackfan Diamond Anemia

Blackfan-Diamond Disease

Blackfan-Diamond Syndrome

Chronic Congenital Agenerative Anemia

Congenital Erythroid Hypoplastic Anemia

Congenital Hypoplastic Anemia Of Blackfan And Diamond

Congenital Pure Red Cell Anemia

Hypoplastic Congenital Anemia

Inherited Erythroblastopenia

Pure Hereditary Red Cell Aplasia

Anemia, Hypoplastic, Congenital

Anemia Hypoplastic Congenital

Fanconi Anemia

Constitutional Aplastic Anemia

Diamond-Blackfan Anemia 1

Aase Smith Syndrome 2

Congenital Red Cell Aplasia

Red Cell Aplasia Of Infants

Pure Red Cell Aplasia Of Infants

Congenital Red Cell Aplastic Anaemia

Congenital Pure Red Cell Anaemia

Congenital Erythroid Hypoplasia

Pearson Marrow-Pancreas Syndrome

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

Orthologs Information

Species Symbol Source ID
Macaca mulatta GNL3 VGNC VGNC:73038
Canis familiaris GNL3 VGNC VGNC:41327
Rattus norvegicus GNL3 RGD RGD:631354
Felis catus GNL3 VGNC VGNC:62626
Bos taurus GNL3 VGNC VGNC:29473
Mus musculus GNL3 MGD MGI:1353651