Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: BPIFA2C ENSBTAG00000031376

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Description

BPI fold containing family A, member 2C [Source:NCBI gene (formerly Entrezgene);Acc:618389]

Gene Synonyms

BSP30C

Location

Primary_assembly 13: 62,565,989-62,575,207 forward strand.

ARS-UCD1.3:CM008180.2

About this gene

This gene has 1 transcript (splice variant), 69 orthologues and 16 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000044455.3	BPIFA2C-201	1099	251aa	ENSBTAP00000041949.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q0PH99	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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