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

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Gene: tbx1 ENSDARG00000031891

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Description

T-box transcription factor 1 [Source:NCBI gene;Acc:368206]

Gene Synonyms

mp:zf637-3-000616, van gogh, vgo, zgc:136724

Location

Chromosome 5: 15,202,495-15,215,483 forward strand.

GRCz11:CM002889.2

About this gene

This gene has 2 transcripts (splice variants), 193 orthologues, 23 paralogues and is associated with 131 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000040826.6	tbx1-201	2343	460aa	ENSDARP00000040825.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8AXX2	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,
ENSDART00000144915.3	tbx1-202	1500	468aa	ENSDARP00000118808.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B8JJ43	APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5,

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Summary

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