Gene: RN7SL790P ENSG00000239745

Description

RNA, 7SL, cytoplasmic 790, pseudogene [Source:HGNC Symbol;Acc:HGNC:46806]

Location

Chromosome X: 74,390,692-74,390,989 forward strand.

GRCh38:CM000685.2

About this gene

This gene has 1 transcript (splice variant), 18 orthologues and 847 paralogues.

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	RefSeq Match	Flags
ENST00000474043.3	RN7SL790P-201	298	No protein	-	misc RNA		-	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic, TSL NA: A transcript that was not analysed for TSL. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:NA,

Variant image

Retirement notice

Human only - retirement of this view

As of Ensembl release 93 this view will no longer be available for human, because we feel that the density of known human genetic variation is too great for the display to be informative in its current form.

Other species will not be affected, as they have less variation data.

For more information about the decision and on how to find variation data for a gene, please see our blog post.

Gene: RN7SL790P ENSG00000239745

Variant image

Retirement notice

Human only - retirement of this view

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Gene: RN7SL790P ENSG00000239745

Variant image

Retirement notice

Human only - retirement of this view

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