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

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Gene: Napg ENSRNOG00000018914

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Description

NSF attachment protein gamma [Source:RGD Symbol;Acc:1310109]

Gene Synonyms

LOC307382

Location

Primary_assembly 18: 58,708,655-58,729,450 forward strand.

GRCr8:CM070408.1

About this gene

This gene has 2 transcripts (splice variants), 233 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000065802.4	Napg-201	3563	312aa	ENSRNOP00000061787.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IXL2 D4A0E2	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,
ENSRNOT00000077726.3	Napg-202	3666	295aa	ENSRNOP00000072502.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K350	-

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Summary

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