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

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Gene: NSF ENSBTAG00000008442

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Description

N-ethylmaleimide sensitive factor, vesicle fusing ATPase [Source:VGNC Symbol;Acc:VGNC:32274]

Location

Primary_assembly 19: 45,443,488-45,591,602 reverse strand.

ARS-UCD2.0:CM008186.2

About this gene

This gene has 5 transcripts (splice variants) and 285 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000086265.2	NSF-205	3362	771aa	ENSBTAP00000063277.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LSE5	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,
ENSBTAT00000083265.1	NSF-201	3914	752aa	ENSBTAP00000074503.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MR04	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,
ENSBTAT00000090314.1	NSF-202	3623	655aa	ENSBTAP00000076146.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RYF6	-
ENSBTAT00000011107.6	NSF-203	3527	623aa	ENSBTAP00000011107.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MZU2	-
ENSBTAT00000115930.1	NSF-204	3476	606aa	ENSBTAP00000100261.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TNW1	-

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Summary

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