Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
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: IFI44 ENSPTRG00000000893

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Description

interferon induced protein 44 [Source:VGNC Symbol;Acc:VGNC:6881]

Location

Chromosome 1: 78,772,743-78,786,954 forward strand.

Pan_tro_3.0:CM000314.3

About this gene

This gene has 1 transcript (splice variant), 1013 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000001694.4	IFI44-201	1638	444aa	ENSPTRP00000001546.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A663DB11 K7BX63 P27473	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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