Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Gene: NAIF1 ENSOGAG00000031498

Description

nuclear apoptosis inducing factor 1 [Source:HGNC Symbol;Acc:HGNC:25446]

Location

About this gene

This gene has 1 transcript (splice variant) and 192 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOGAT00000024133.1	NAIF1-201	1017	338aa	ENSOGAP00000019949.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H0XV07	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,

Summary