CMSS1 - cms1 ribosomal small subunit homolog Gene

Homo sapiens

Also known as C3orf26

Gene ID: 84319 | Gene type: protein coding

About CMSS1

This gene has 9 transcripts (splice variants) and 205 orthologues. Ubiquitous expression in testis (RPKM 15.9), adrenal (RPKM 15.4) and 25 other tissues.

Summary

Enables RNA binding activity. [provided by Alliance of Genome Resources, Apr 2022]

CMSS1 Products(2)

mRNA	Protein	Name
NM_001167924.2	NP_001161396.1	protein CMSS1 isoform 2
NM_032359.4	NP_115735.2	protein CMSS1 isoform 1

Gene Ontology

Molecular Function

Molecular Function GO Annotation	Evidence	Reference	Source
enables protein binding	IPI IPI: Inferred from physical interaction	32814053	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

CMSS1 Protein Structure

CMS1

0
100
200
279 a.a.

Protein Preferred Names

Protein Names

protein CMSS1

CMSS1 Protein-protein interaction Information

Type Cross Intra	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	Reference
Intra	CMSS1	Q9BQ75	WFS1	Homo sapiens	O76024	Validated Y2H	32814053
Intra	CMSS1	Q9BQ75	WFS1	Homo sapiens	O76024	Y2H Array	32814053
Intra	CMSS1	Q9BQ75	WFS1	Homo sapiens	O76024	Y2H Pooling	32814053

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases

Alias

Robinow Syndrome, Autosomal Recessive 1

Robinow Syndrome, Autosomal Recessive	Autosomal Recessive Robinow Syndrome
Covesdem Syndrome	RRS1
Costovertebral Segmentation Defect-Mesomelia Syndrome	Rrs
Costovertebral Segmentation Defect With Mesomelia, Formerly	Covesdem Syndrome, Formerly
Costovertebral Segmentation Defect With Mesomelia	Robinow Syndrome Autosomal Recessive With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals
Robinow Syndrome Autosomal Recessive With Brachy-Syn-Polydactyly	Robinow Syndrome, Autosomal Recessive, With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals
Robinow Syndrome, Autosomal Recessive, With Brachy-Syn-Polydactyly	Robinow, Autosomal Recessive Syndrome, Type 1

Nanophthalmos

Nanophthalmia

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-RS02863	CMSS1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	CMSS1	VGNC	VGNC:59067
Macaca mulatta	CMSS1	VGNC	VGNC:71365
Felis catus	CMSS1	VGNC	VGNC:102676
Bos taurus	CMSS1	VGNC	VGNC:96694
Rattus norvegicus	CMSS1	RGD	RGD:1309437
Mus musculus	CMSS1	MGD	MGI:1913747

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