Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Narf ENSRNOG00000036664

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Description

nuclear prelamin A recognition factor [Source:RGD Symbol;Acc:1310894]

Gene Synonyms

IOP2, LOC102550455, LOC360681, MGC125093, RGD1310894

Location

Primary_assembly 10: 107,016,510-107,037,283 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 3 transcripts (splice variants), 216 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000123728.1	Narf-203	1729	506aa	ENSRNOP00000112220.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000054920.4	Narf-201	4894	493aa	ENSRNOP00000051803.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QR57	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,
ENSRNOT00000099773.2	Narf-202	4491	470aa	ENSRNOP00000080579.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZR12	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,

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Summary

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