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

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Gene: Nwd2 ENSRNOG00000051837

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Description

NACHT and WD repeat domain containing 2 [Source:RGD Symbol;Acc:1563065]

Gene Synonyms

LOC103694210, LOC289633, RGD1563065

Location

Primary_assembly 14: 44,834,856-45,024,047 reverse strand.

GRCr8:CM070404.1

About this gene

This gene has 2 transcripts (splice variants), 211 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000079269.3	Nwd2-201	6465	1754aa	ENSRNOP00000071171.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JZT1	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,
ENSRNOT00000169156.1	Nwd2-202	6225	1674aa	ENSRNOP00000105461.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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