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: Nalf2 ENSRNOG00000038066

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Description

NALCN channel auxiliary factor 2 [Source:RGD Symbol;Acc:1584125]

Gene Synonyms

Fam155b, LOC688841, Tmem28l

Location

Primary_assembly X: 68,965,327-68,991,201 forward strand.

GRCr8:CM070411.1

About this gene

This gene has 1 transcript (splice variant), 142 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000057920.5	Nalf2-201	4760	471aa	ENSRNOP00000054729.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A4E6	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,

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Summary

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