Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: sec61a1l ENSDARG00000005675

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Description

SEC61 translocon alpha 1 subunit, like [Source:NCBI gene;Acc:266796]

Gene Synonyms

cb413, sec61al2, sec61b, wu:fb36f05, wu:fb36f12, wu:fb37d04, wu:fi26f11

Location

Chromosome 6: 42,377,911-42,388,608 reverse strand.

GRCz11:CM002890.2

About this gene

This gene has 2 transcripts (splice variants), 281 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000049425.7	sec61a1l-201	2553	476aa	ENSDARP00000049424.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0J9YIG5	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,
ENSDART00000143910.2	sec61a1l-202	687	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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