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

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Gene: Sec13 ENSRNOG00000010628

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Description

SEC13 homolog, nuclear pore and COPII coat complex component [Source:RGD Symbol;Acc:1359555]

Gene Synonyms

MGC105923, Sec13l1

Location

Primary_assembly 4: 148,433,349-148,446,755 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 3 transcripts (splice variants), 224 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000014377.6	Sec13-201	1289	322aa	ENSRNOP00000014377.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q6Q3 A6IBU1	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,
ENSRNOT00000114125.2	Sec13-203	1941	295aa	ENSRNOP00000077650.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5XFW8	-
ENSRNOT00000106299.2	Sec13-202	1213	314aa	ENSRNOP00000091682.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ATA8	-

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Summary

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