1. Gene
  2. PELO - pelota mRNA surveillance and ribosome rescue factor Gene

PELO - pelota mRNA surveillance and ribosome rescue factor Gene

Homo sapiens

Also known as CGI-17; PRO1770

Gene ID: 53918 | Gene type: protein coding

About PELO

Cytogenetic location: 5q11.2 Genomic coordinates (GRCh38): 5:52,787,916-52,804,044 (from NCBI)

This gene has 2 transcripts (splice variants) and 189 orthologues. Ubiquitous expression in adrenal (RPKM 14.2), spleen (RPKM 12.3) and 25 other tissues.

Summary

This gene encodes a protein which contains a conserved nuclear localization signal. The encoded protein may have a role in spermatogenesis, cell cycle control, and in meiotic cell division. [provided by RefSeq, Jul 2008]

PELO Products(1)

mRNA Protein Name
NM_015946.5 NP_057030.3 protein pelota homolog
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
20406461 GOA
enables ribosome binding IDA
IDA: Inferred from direct assay
27543824 GOA
enables stalled ribosome sensor activity IDA
IDA: Inferred from direct assay
27863242 GOA
Biological Process GO Annotation Evidence Reference Source
involved in nuclear-transcribed mRNA catabolic process, no-go decay IDA
IDA: Inferred from direct assay
23667253 GOA
involved in rescue of stalled ribosome IDA
IDA: Inferred from direct assay
21448132 GOA
involved in ribosome disassembly IDA
IDA: Inferred from direct assay
21448132 GOA
Cellular Component GO Annotation Evidence Reference Source
part of Dom34-Hbs1 complex IDA
IDA: Inferred from direct assay
27863242 GOA
is active in cytosolic ribosome IDA
IDA: Inferred from direct assay
27863242 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

PELO Protein Structure

eRF1_1

eRF1_1: eRF1 domain 1 (1 - 130)

eRF1_2

eRF1_2: eRF1 domain 2 (136 - 268)

eRF1_3

eRF1_3: eRF1 domain 3 (272 - 370)

  • 0
  • 100
  • 200
  • 300
  • 385 a.a.
Protein Preferred Names Protein Names

protein pelota homolog

pelota homolog

PELO Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
PELO Q9BRX2 KRTAP12-2 Homo sapiens P59991 32296183
Intra
PELO Q9BRX2 KRTAP12-2 Homo sapiens P59991 32296183
Intra
PELO Q9BRX2 ICAM1 Homo sapiens P05362 32814053
Intra
PELO Q9BRX2 ICAM1 Homo sapiens P05362 32814053
Intra
PELO Q9BRX2 ICAM1 Homo sapiens P05362 32814053
Intra
PELO Q9BRX2 MAT2A Homo sapiens P31153 32814053
Intra
PELO Q9BRX2 MAT2A Homo sapiens P31153 32814053
Intra
PELO Q9BRX2 MAT2A Homo sapiens P31153 32814053
Intra
PELO Q9BRX2 KIF1B Homo sapiens O60333-2 32814053
Intra
PELO Q9BRX2 KIF1B Homo sapiens O60333-2 32814053
Intra
PELO Q9BRX2 KIF1B Homo sapiens O60333-2 32814053
Intra
PELO Q9BRX2 LMO3 Homo sapiens Q8TAP4-4 32296183
Intra
PELO Q9BRX2 LMO3 Homo sapiens Q8TAP4-4 32296183
Intra
PELO Q9BRX2 DYNLT1 Homo sapiens P63172 32296183
Intra
PELO Q9BRX2 DYNLT1 Homo sapiens P63172 32296183
Intra
PELO Q9BRX2 PRKCA Homo sapiens P17252 32814053
Intra
PELO Q9BRX2 PRKCA Homo sapiens P17252 32814053
Intra
PELO Q9BRX2 PRKCA Homo sapiens P17252 32814053
Intra
PELO Q9BRX2 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
PELO Q9BRX2 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
PELO Q9BRX2 SRPX Homo sapiens P78539 20406461
Intra
PELO Q9BRX2 SRPX Homo sapiens P78539
Y2H
20406461
Intra
PELO Q9BRX2 SRPX Homo sapiens P78539 20406461
Intra
PELO Q9BRX2 SRPX Homo sapiens P78539 20406461
Intra
PELO Q9BRX2 SRPX Homo sapiens P78539 20406461
Intra
PELO Q9BRX2 PPIA Homo sapiens P62937-2 32814053
Intra
PELO Q9BRX2 PPIA Homo sapiens P62937-2 32814053
Intra
PELO Q9BRX2 PPIA Homo sapiens P62937-2 32814053
Intra
PELO Q9BRX2 HBS1L Homo sapiens Q9Y450 32296183
Intra
PELO Q9BRX2 HBS1L Homo sapiens Q9Y450 31515488
Intra
PELO Q9BRX2 HBS1L Homo sapiens Q9Y450 32296183
Intra
PELO Q9BRX2 HBS1L Homo sapiens Q9Y450 32296183
Intra
PELO Q9BRX2 HSPB1 Homo sapiens P04792 32814053
Intra
PELO Q9BRX2 HSPB1 Homo sapiens P04792 32814053
Intra
PELO Q9BRX2 HSPB1 Homo sapiens P04792 32814053
Intra
PELO Q9BRX2 HAX1 Homo sapiens O00165 20406461
Intra
PELO Q9BRX2 HAX1 Homo sapiens O00165 20406461
Intra
PELO Q9BRX2 HAX1 Homo sapiens O00165 20406461
Intra
PELO Q9BRX2 HAX1 Homo sapiens O00165 20406461
Intra
PELO Q9BRX2 HAX1 Homo sapiens O00165
Y2H
20406461
Intra
PELO Q9BRX2 YWHAG Homo sapiens P61981 32814053
Intra
PELO Q9BRX2 YWHAG Homo sapiens P61981 32814053
Intra
PELO Q9BRX2 YWHAG Homo sapiens P61981 32814053
Intra
PELO Q9BRX2 KAT5 Homo sapiens Q92993 32814053
Intra
PELO Q9BRX2 KAT5 Homo sapiens Q92993 32814053
Intra
PELO Q9BRX2 KAT5 Homo sapiens Q92993 32814053
Intra
PELO Q9BRX2 NEFL Homo sapiens P07196 32814053
Intra
PELO Q9BRX2 NEFL Homo sapiens P07196 32814053
Intra
PELO Q9BRX2 NEFL Homo sapiens P07196 32814053
Intra
PELO Q9BRX2 WFS1 Homo sapiens O76024 32814053
Intra
PELO Q9BRX2 WFS1 Homo sapiens O76024 32814053
Intra
PELO Q9BRX2 WFS1 Homo sapiens O76024 32814053
Intra
PELO Q9BRX2 BAG3 Homo sapiens O95817 32814053
Intra
PELO Q9BRX2 BAG3 Homo sapiens O95817 32814053
Intra
PELO Q9BRX2 BAG3 Homo sapiens O95817 32814053
Intra
PELO Q9BRX2 PRPS1 Homo sapiens P60891 32814053
Intra
PELO Q9BRX2 PRPS1 Homo sapiens P60891 32814053
Intra
PELO Q9BRX2 PRPS1 Homo sapiens P60891 32814053
Intra
PELO Q9BRX2 SETDB1 Homo sapiens Q15047-2 32814053
Intra
PELO Q9BRX2 SETDB1 Homo sapiens Q15047-2 32814053
Intra
PELO Q9BRX2 SETDB1 Homo sapiens Q15047-2 32814053
Intra
PELO Q9BRX2 FLNA Homo sapiens P21333-2 32296183
Intra
PELO Q9BRX2 FLNA Homo sapiens P21333-2 32814053
Intra
PELO Q9BRX2 FLNA Homo sapiens P21333-2 32814053
Intra
PELO Q9BRX2 FLNA Homo sapiens P21333-2 32814053
Intra
PELO Q9BRX2 FLNA Homo sapiens P21333-2 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Progressive Myoclonus Epilepsy 10

Early-Onset Lafora Body Disease

Epm10

Sveinsson Chorioretinal Atrophy

SCRA

Atrophia Areata

Helicoid Peripapillary Chorioretinal Degeneration

Hpcd

Aa

Peripapillary Chorioretinal Degeneration, Icelandic Type

Helicoidal Peripapillary Chorioretinal Degeneration

Atrophy, Chorioretinal, Sveinsson

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
Mus musculus PELO MGD MGI:2145154
Rattus norvegicus PELO RGD RGD:1359591
Bos taurus PELO VGNC VGNC:32743
Felis catus PELO VGNC VGNC:102287
Macaca mulatta PELO VGNC VGNC:84478