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

Configure this page

Share this page

Bookmark this page

.

Gene: SNX21 ENSSSCG00000007425

.

Description

sorting nexin family member 21 [Source:VGNC Symbol;Acc:VGNC:95758]

Location

Primary_assembly 17: 48,033,717-48,040,522 forward strand.

Sscrofa11.1:CM000828.5

About this gene

This gene has 2 transcripts (splice variants), 192 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000008128.4	SNX21-201	2324	364aa	ENSSSCP00000007912.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1U0Y9 F1SC77	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,
ENSSSCT00000083876.1	SNX21-202	2466	218aa	ENSSSCP00000070275.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0SZD4 A0A8D1GM92	-

.

Summary

.

.