CMSS1 - cms1 ribosomal small subunit homolog Gene

Also Known as C3orf26

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 84319

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 References 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

CMS1: U3-containing 90S pre-ribosomal complex subunit (63 - 263)

  • 0
  • 100
  • 200
  • 279 a.a.
Protein Preferred Names Protein Names

protein CMSS1

CMSS1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
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

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 Set / 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
Others CMSS1 NCBI