Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
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  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: TIRAP ENSBTAG00000021504

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Description

TIR domain containing adaptor protein [Source:VGNC Symbol;Acc:VGNC:35879]

Location

Primary_assembly 29: 29,629,109-29,647,270 forward strand.

ARS-UCD2.0:CM008196.2

About this gene

This gene has 4 transcripts (splice variants) and 187 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000070781.3	TIRAP-202	5891	327aa	ENSBTAP00000065132.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M4J2	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000149287.1	TIRAP-203	4065	232aa	ENSBTAP00000105963.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q2LGB6	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSBTAT00000028660.6	TIRAP-204	3843	231aa	ENSBTAP00000028660.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6PZW4	-
ENSBTAT00000069526.3	TIRAP-201	2017	226aa	ENSBTAP00000071038.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MNE1	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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