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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: TBX2 ENSG00000121068

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Description

T-box 2 [Source:HGNC Symbol;Acc:11597]

Location

Chromosome 17: 59,477,257-59,486,827 forward strand.

GRCh37:CM000679.1

About this gene

This gene has 4 transcripts (splice variants) and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000240328.3	TBX2-001	3339	712aa	ENSP00000240328.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS11627	Q13207	NM_005994.3	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000419047.1	TBX2-002	3344	146aa	ENSP00000404781.1	Nonsense mediated decay		F8WCM9	-	-
ENST00000586986.1	TBX2-005	329	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-
ENST00000477081.1	TBX2-003	5218	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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