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: BPIFB6 ENSPTRG00000013388

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Description

BPI fold containing family B member 6 [Source:VGNC Symbol;Acc:VGNC:6060]

Location

Chromosome 20: 34,403,779-34,416,170 forward strand.

Pan_tro_3.0:CM000334.4

About this gene

This gene has 1 transcript (splice variant), 88 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000024863.4	BPIFB6-201	1362	453aa	ENSPTRP00000022948.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2X7F1 H2QK65	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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