1. Gene
  2. RPS28 - ribosomal protein S28 Gene

RPS28 - ribosomal protein S28 Gene

Homo sapiens

Also known as S28; eS28; DBA15

Gene ID: 6234 | Gene type: protein coding

About RPS28

Cytogenetic location: 19p13.2 Genomic coordinates (GRCh38): 19:8,321,496-8,323,340 (from NCBI)

This gene has 4 transcripts (splice variants), 189 orthologues and is associated with 2 phenotypes. Ubiquitous expression in ovary (RPKM 563.4), spleen (RPKM 434.5) 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 S28E 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]

RPS28 Products(1)

mRNA Protein Name
NM_001031.5 NP_001022.1 40S ribosomal protein S28

RPS28 Protein Structure

Ribosomal_S28e

Ribosomal_S28e: Ribosomal protein S28e (1 - 69)

  • 0
  • 69 a.a.
Protein Preferred Names Protein Names

40S ribosomal protein S28

small ribosomal subunit protein eS28

Related Diseases

Diseases Alias
Diamond-Blackfan Anemia 15 With Mandibulofacial Dysostosis

DBA15

Diamond Blackfan Anemia 15 With Mandibulofacial Dysostosis

Diamond-Blackfan Anemia 15, With Mandibulofacial Dysostosis

Diamond-Blackfan Anemia With Microtia And Cleft Palate

Anemia, Diamond Blackfan, Type 15 With Mandibulofacial Dysostosis

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

Macrocytic Anemia

Anemia Macrocytic

Anemia, Macrocytic

Macrocytic Anaemia

Diamond-Blackfan Anemia 10

DBA10

Rps26-Related Diamond-Blackfan Anemia

Anemia, Diamond-Blackfan, Type 10

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

Erythrasma

Infection Due To Corynebacterium Minutissimum

Dysostosis

Dysostoses

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

Dyskeratosis Congenita

Dyskeratosis Congenita Autosomal Dominant

Dc

Dkc

Zinsser-Engman-Cole Syndrome

Dyskeratosis Congenita, Autosomal Dominant

Autosomal Dominant Dyskeratosis Congenita

Dkca

Dyskeratosis Congenita Scoggins Type

Zinsser-Cole-Engman Syndrome

X-Linked Dyskeratosis Congenita

Hoyeraal-Hreidarsson 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
Felis catus RPS28 VGNC VGNC:80709
Mus musculus RPS28 MGD MGI:1859516
Rattus norvegicus RPS28 RGD RGD:621046
Bos taurus RPS28 VGNC VGNC:34136
Canis familiaris RPS28 VGNC VGNC:108256