Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: NALF2 ENSBTAG00000011310

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Description

NALCN channel auxiliary factor 2 [Source:VGNC Symbol;Acc:VGNC:28736]

Gene Synonyms

FAM155B

Location

Primary_assembly X: 80,933,030-80,960,400 reverse strand.

ARS-UCD1.3:CM008197.2

About this gene

This gene has 1 transcript (splice variant), 143 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000045942.5	NALF2-201	2622	473aa	ENSBTAP00000043288.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3X7U0	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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