Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Bcl2l14 ENSRNOG00000028632

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Description

Bcl2-like 14 [Source:RGD Symbol;Acc:1562777]

Gene Synonyms

LOC500348

Location

Primary_assembly 4: 168,948,946-168,990,079 forward strand.

GRCr8:CM070394.1

About this gene

This gene has 2 transcripts (splice variants), 162 orthologues, 1 paralogue and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000032229.7	Bcl2l14-201	2339	326aa	ENSRNOP00000029468.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IMD0 Q6AYK4	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,
ENSRNOT00000173534.1	Bcl2l14-202	2268	298aa	ENSRNOP00000104674.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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