Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Bid ENSRNOG00000012439

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Description

BH3 interacting domain death agonist [Source:RGD Symbol;Acc:620160]

Location

Primary_assembly 4: 155,785,377-155,808,275 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 2 transcripts (splice variants), 90 orthologues and is associated with 13 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000096502.2	Bid-202	594	197aa	ENSRNOP00000078364.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZKS3	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,
ENSRNOT00000016776.4	Bid-201	1992	196aa	ENSRNOP00000016776.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A8ASI9 Q9JLT6	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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