small ribosomal subunit protein mS22 isoform 2 [Homo sapiens]

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Find regions of similarity between this sequence and other sequences using BLAST.
Identify Conserved Domains
View conserved domains detected in this protein sequence using CD-search.
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Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.

A patient with mitochondrial disorder due to a novel mutation in MRPS22. [Metab Brain Dis. 2017]
A patient with mitochondrial disorder due to a novel mutation in MRPS22.
Kılıç M, Oğuz KK, Kılıç E, Yüksel D, Demirci H, Sağıroğlu MŞ, Yücel-Yılmaz D, Özgül RK. Metab Brain Dis. 2017 Oct; 32(5):1389-1393. Epub 2017 Jul 27.
Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy. [Eur J Hum Genet. 2011]
Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy.
Smits P, Saada A, Wortmann SB, Heister AJ, Brink M, Pfundt R, Miller C, Haas D, Hantschmann R, Rodenburg RJ, et al. Eur J Hum Genet. 2011 Apr; 19(4):394-9. Epub 2010 Dec 29.
Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation. [J Med Genet. 2007]
Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation.
Saada A, Shaag A, Arnon S, Dolfin T, Miller C, Fuchs-Telem D, Lombes A, Elpeleg O. J Med Genet. 2007 Dec; 44(12):784-6. Epub 2007 Sep 14.

RefSeq genomic sequence
See the genomic reference sequence for the MRPS22 gene (NG_012174.1).
RefSeq mRNA
See reference mRNA sequence for the MRPS22 gene (NM_001363857.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the MRPS22 gene.