Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Tasor2 ENSRNOG00000018011

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Description

transcription activation suppressor family member 2 [Source:RGD Symbol;Acc:1564456]

Gene Synonyms

Fam208b, LOC361269, RGD1564456

Location

Primary_assembly 17: 71,504,822-71,559,035 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 4 transcripts (splice variants), 201 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000126636.1	Tasor2-204	8665	2384aa	ENSRNOP00000098852.1	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, 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,
ENSRNOT00000048933.8	Tasor2-201	8322	2384aa	ENSRNOP00000051465.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZVI2	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,
ENSRNOT00000118354.2	Tasor2-203	8259	2363aa	ENSRNOP00000082595.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZTT1	-
ENSRNOT00000096239.2	Tasor2-202	8196	2342aa	ENSRNOP00000082153.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZTH0	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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