RN7SL2 - RNA component of signal recognition particle 7SL2 Gene

Also Known as 7L1C; 7SL1c; 7L30.1; RNSRP2

Species: Homo sapiens

Gene Type: scRNA
Gene ID: 378706

About RN7SL2

Cytogenetic location: 14q21.3 Genomic coordinates (GRCh38): 14:49,862,551-49,862,849 (from NCBI)

This gene has 1 transcript (splice variant), 27 orthologues and 847 paralogues.

Summary

The signal recognition particle (SRP) is a cytoplasmic ribonucleoprotein complex that mediates cotranslational insertion of secretory proteins into the lumen of the endoplasmic reticulum. The SRP consists of 6 polypeptides (e.g., SRP19; MIM 182175) and a 7SL RNA molecule, such as RN7SL2, that is partially homologous to Alu DNA (Ullu and Weiner, 1984 [PubMed 6084597]).[supplied by OMIM, Jul 2008]

Related Diseases

Diseases Alias
Alopecia-Mental Retardation Syndrome
Alopecia-Mental Retardation Syndrome 1

  • APMR1

  • Alopecia-Intellectual Disability Syndrome 1

  • Amr Syndrome

  • Alopecia-Intellectual Disability Syndrome

  • Amr Syndrome 1

  • Alopecia With Severe Intellectual Deficit

  • Apmr

  • Alopecia Intellectual Disbility Syndrome 1

  • Perniola-Krajewska-Carnevale Syndrome

  • Alopecia - Intellectual Disability Syndrome

  • Alopecia With Mental Retardation Syndrome 1

  • Perniola Krajewska Carnevale 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