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

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Gene: tax1bp1b ENSDARG00000056856

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Description

Tax1 (human T-cell leukemia virus type I) binding protein 1b [Source:NCBI gene (formerly Entrezgene);Acc:324152]

Location

Chromosome 16: 20,805,322-20,932,896 reverse strand.

GRCz11:CM002900.2

About this gene

This gene has 4 transcripts (splice variants), 219 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000040727.8	tax1bp1b-201	3271	810aa	ENSDARP00000040726.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSDART00000180646.1	tax1bp1b-203	3813	843aa	ENSDARP00000153930.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSDART00000188905.1	tax1bp1b-204	3686	794aa	ENSDARP00000145329.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8PWM5	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,
ENSDART00000169541.2	tax1bp1b-202	3202	822aa	ENSDARP00000137903.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AB13AAL3	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,

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Summary

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