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
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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Molecular interactions
External references
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ID History
- Gene history

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Gene: NMD3 ENSBTAG00000016228

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Description

NMD3 ribosome export adaptor [Source:VGNC Symbol;Acc:VGNC:32125]

Location

Primary_assembly 1: 106,135,036-106,187,628 reverse strand.

ARS-UCD2.0:CM008168.2

About this gene

This gene has 3 transcripts (splice variants) and 212 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000116795.1	NMD3-203	3049	526aa	ENSBTAP00000095825.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TG44	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000021594.7	NMD3-202	2948	514aa	ENSBTAP00000021594.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF6Z2A6	-
ENSBTAT00000127502.1	NMD3-201	1701	503aa	ENSBTAP00000084053.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SJR1	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Summary

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