RPS17

GENE INFORMATION

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Gene name

RPS17 (HGNC Symbol)

Synonyms

MGC72007, RPS17L, RPS17L1, RPS17L2, S17

Description

Ribosomal protein S17 (HGNC Symbol)

Entrez gene 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 four 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 S17E family of ribosomal proteins and is located in the cytoplasm. Mutations in this gene cause Diamond-Blackfan anemia 4. Alternative splicing of this gene results in multiple transcript variants. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Apr 2014]

Chromosome

15

Cytoband

q25.2

Chromosome location (bp)

82536753 - 82540564

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000182774 (version 78.38)

Entrez gene

6218

UniProt

P08708 (UniProt - Evidence at protein level), P0CW22 (UniProt - Evidence at protein level)

neXtProt

NX_P08708, NX_P0CW22

Antibodypedia

RPS17 antibodies
 

PROTEIN VIEW

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RPS17-001
 
RPS17-005
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

RPS17-001 ENSP00000346046
ENST00000330244
P08708
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Show » Show » 135 15.5 No 0
RPS17-005 ENSP00000453910
ENST00000561157
H0YN88
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Show » Show » 136 15.9 No 0