Human (GRCh38.p14)
Description

RNA, 7SL, cytoplasmic 262, pseudogene [Source:HGNC Symbol;Acc:HGNC:46278]

Location

Chromosome X: 49,152,651-49,152,944 forward strand.

GRCh38:CM000685.2

View alleles of this gene on alternative sequences

About this gene

This gene has 1 transcript (splice variant), 1 gene allele, 5 orthologues and 847 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000584590.2RN7SL262P-201294No protein-
 
misc RNA
-Ensembl CanonicalGENCODE basicTSL:NA