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

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Gene: NAIF1 ENSGALG00010028061

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Description

nuclear apoptosis inducing factor 1 [Source:NCBI gene (formerly Entrezgene);Acc:417229]

Gene Synonyms

C9orf90

Location

Primary_assembly 17: 5,495,685-5,499,907 forward strand.

bGalGal1.mat.broiler.GRCg7b:CM028498.1

About this gene

This gene has 2 transcripts (splice variants), 192 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010067995.1	NAIF1-202	2460	346aa	ENSGALP00010041738.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V1ABX9	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 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,
ENSGALT00010067997.1	NAIF1-201	3035	332aa	ENSGALP00010041740.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V1AET7	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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