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

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Gene: SSR2 ENSSSCG00000006501

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Description

signal sequence receptor subunit 2 [Source:VGNC Symbol;Acc:VGNC:93491]

Location

Primary_assembly 4: 94,011,527-94,021,962 forward strand.

Sscrofa11.1:CM000815.5

About this gene

This gene has 3 transcripts (splice variants) and 203 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000081263.2	SSR2-202	779	183aa	ENSSSCP00000069438.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A480W8D2 A0A4X1W122	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,
ENSSSCT00000007120.5	SSR2-203	571	86aa	ENSSSCP00000006928.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1VZX8 F1RLP7	-
ENSSSCT00000045600.3	SSR2-201	567	182aa	ENSSSCP00000053510.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BAH7 A0A8D1CTI5	-

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Summary

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