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: BPIFA3 ENSPTRG00000013393

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Description

BPI fold containing family A member 3 [Source:VGNC Symbol;Acc:VGNC:6056]

Location

Chromosome 20: 34,605,338-34,615,868 forward strand.

Pan_tro_3.0:CM000334.4

About this gene

This gene has 2 transcripts (splice variants), 99 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000024874.4	BPIFA3-201	1246	250aa	ENSPTRP00000022959.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XCX4 H2QK66	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,
ENSPTRT00000086131.1	BPIFA3-202	657	218aa	ENSPTRP00000087021.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TCT8 A0A6D2W297	-

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Summary

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