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

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Gene: NARF ENSBTAG00000018178

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Description

nuclear prelamin A recognition factor [Source:VGNC Symbol;Acc:VGNC:55858]

Location

Primary_assembly 19: 50,100,748-50,118,270 reverse strand.

ARS-UCD2.0:CM008186.2

About this gene

This gene has 2 transcripts (splice variants), 215 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000113724.1	NARF-201	2398	441aa	ENSBTAP00000086661.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SRG3	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,
ENSBTAT00000024191.6	NARF-202	1832	408aa	ENSBTAP00000024191.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MEC7	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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