Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: NWD2 ENSSSCG00000008770

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Description

NACHT and WD repeat domain containing 2 [Source:VGNC Symbol;Acc:VGNC:90992]

Location

Primary_assembly 8: 28,801,568-29,009,163 forward strand.

Sscrofa11.1:CM000819.5

About this gene

This gene has 2 transcripts (splice variants), 212 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000054199.2	NWD2-202	8452	1742aa	ENSSSCP00000048301.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AVZ9	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,
ENSSSCT00000057459.1	NWD2-201	1185	121aa	ENSSSCP00000046704.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AS13 A0A4X1V7A9	-

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Summary

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