RN7SL2 - RNA component of signal recognition particle 7SL2 Gene

Homo sapiens

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

Gene ID: 378706 | Gene type: scRNA

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

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