RPS25 - ribosomal protein S25 Gene

Homo sapiens

Also known as S25

Gene ID: 6230 | Gene type: protein coding

About RPS25

Cytogenetic location: 11q23.3 Genomic coordinates (GRCh38): 11:119,015,717-119,018,343 (from NCBI)

This gene has 6 transcripts (splice variants), 1 gene allele and 201 orthologues. Ubiquitous expression in ovary (RPKM 1368.6), lymph node (RPKM 772.3) and 25 other tissues.

Summary

Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S25E family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]

RPS25 Products(1)

mRNA	Protein	Name
NM_001028.3	NP_001019.1	40S ribosomal protein S25

RPS25 Protein Structure

Ribosomal_S25

0
100
125 a.a.

Protein Preferred Names

Protein Names

40S ribosomal protein S25

small ribosomal subunit protein eS25

Related Diseases

Diseases

Alias

Chromosome 5q Deletion Syndrome

5q- Syndrome	Mar
Myelodysplastic Syndrome Associated With Isolated Del Chromosome Abnormality	Macrocytic Anemia, Refractory, Due To 5q Deletion, Somatic
5q Deletion Syndrome	5q Minus Syndrome
Refractory Macrocytic Anemia Due To 5q Deletion	Myelodysplastic Syndrome With Isolated Del
Macrocytic Anemia, Refractory, Due To 5q Deletion	5q- Syndrome, Refractory Macrocytic Anemia Due To 5q Deletion
5q Syndrome	Chromosome 5q Deletion
Myelodysplastic Syndrome With 5q Deletion	Myelodysplastic Syndrome With 5q Deletion Syndrome
Anemia, Macrocytic, Refractory, Due To 5q Deletion, Somatic	5q-Syndrome
Chromosome 5, Trisomy 5q	Loss Of Chromosome 5q
5 Q- Syndrome

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS12236	RPS25 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	RPS25	RGD	RGD:621043
Mus musculus	RPS25	MGD	MGI:1922867

Name
Email *

	Sorry, but the email address you supplied was invalid.