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
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SNW1 ENSSSCG00000022932

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Description

SNW domain containing 1 [Source:VGNC Symbol;Acc:VGNC:93302]

Location

Primary_assembly 7: 100,718,036-100,749,356 reverse strand.

Sscrofa11.1:CM000818.5

About this gene

This gene has 2 transcripts (splice variants) and 234 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000025189.3	SNW1-202	2379	536aa	ENSSSCP00000020257.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1T4R9 I3L897	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,
ENSSSCT00000067034.1	SNW1-201	2335	532aa	ENSSSCP00000061930.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QCT6 A0A8D1SPB0	-

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Summary

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