Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
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ID History
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Gene: AABR07028668.1 ENSRNOG00000060417

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Description

Sec61 translocon subunit gamma like 2 [Source:RGD Symbol;Acc:11394977]

Location

Primary_assembly 17: 80,547,563-80,547,769 reverse strand.

GRCr8:CM070407.1

About this gene

This gene has 1 transcript (splice variant), 257 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000085909.3	AABR07028668.1-201	207	68aa	ENSRNOP00000074173.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K7E7	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, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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