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

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Gene: BNIP3L ENSPTRG00000020097

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Description

BCL2 interacting protein 3 like [Source:HGNC Symbol;Acc:HGNC:1085]

Location

Chromosome 8: 25,832,343-25,856,728 forward strand.

Pan_tro_3.0:CM000322.4

About this gene

This gene has 2 transcripts (splice variants), 299 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000037229.5	BNIP3L-201	3609	219aa	ENSPTRP00000034406.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W7T7 H2QVX5	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,
ENSPTRT00000076575.1	BNIP3L-202	651	216aa	ENSPTRP00000066369.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RNU6	-

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Summary

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