1. Gene
  2. MRTO4 - MRT4 homolog, ribosome maturation factor Gene

MRTO4 - MRT4 homolog, ribosome maturation factor Gene

Homo sapiens

Also known as MRT4; C1orf33; dJ657E11.4

Gene ID: 51154 | Gene type: protein coding

About MRTO4

This gene has 3 transcripts (splice variants) and 227 orthologues. Ubiquitous expression in appendix (RPKM 7.6), lymph node (RPKM 7.5) and 25 other tissues.

Summary

This gene encodes a protein sharing a low level of sequence similarity with ribosomal protein P0. While the precise function of the encoded protein is currently unknown, it appears to be involved in mRNA turnover and ribosome assembly. [provided by RefSeq, Jul 2008]

MRTO4 Products(1)

mRNA Protein Name
NM_016183.4 NP_057267.2 mRNA turnover protein 4 homolog
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
21044950 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

MRTO4 Protein Structure

Ribosomal_L10

Ribosomal_L10: Ribosomal protein L10 (21 - 120)

  • 0
  • 100
  • 200
  • 239 a.a.
Protein Preferred Names Protein Names

mRNA turnover protein 4 homolog

60S acidic ribosomal protein PO

Recombinant MRTO4 Proteins

Cat. No. Product Name Accession Purity
HY-P75465 C1orf33/MRTO4 Protein, Human (His) Q9UKD2 (M1-D239) ≥95%

Related Diseases

Diseases Alias
Branchiootorenal Syndrome 1

Melnick-Fraser Syndrome

BOR1

Branchiootorenal Dysplasia

Branchiootorenal Syndrome 1, With Or Without Cataracts

Bor Syndrome 1

Branchiootorenal Dysplasia 1

Branchio-Oto-Renal Dysplasia 1

Branchio-Oto-Renal Syndrome Type 1

Branchiootorenal Syndrome, With/Without Cataract, Type 1

Branchio-Oto-Renal Syndrome

Shwachman-Diamond Syndrome 1

Shwachman-Diamond Syndrome

Shwachman Syndrome

Shwachman-Bodian-Diamond Syndrome

Sds

Pancreatic Insufficiency And Bone Marrow Dysfunction

Shwachman-Bodian Syndrome

SDS1

Lipomatosis Of Pancreas, Congenital

Congenital Lipomatosis Of Pancreas

Shwachman-Diamond Type Metaphyseal Dysplasia

Metaphyseal Chondrodysplasia, Shwachman Type

Shwachman-Diamond-Oski 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
Mus musculus MRTO4 MGD MGI:1917152
Bos taurus MRTO4 VGNC VGNC:31680
Felis catus MRTO4 VGNC VGNC:63629
Canis familiaris MRTO4 VGNC VGNC:84430
Rattus norvegicus MRTO4 RGD RGD:1311709
Others MRTO4 NCBI