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

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Gene: Tsc2 ENSRNOG00000011375

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Description

TSC complex subunit 2 [Source:RGD Symbol;Acc:3908]

Gene Synonyms

Rc

Location

Primary_assembly 10: 13,621,136-13,655,951 reverse strand.

mRatBN7.2:CM026983.1

About this gene

This gene has 3 transcripts (splice variants), 209 orthologues, 2 paralogues and is associated with 58 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000052138.7	Tsc2-202	5834	1866aa	ENSRNOP00000039381.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZLW4	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,
ENSRNOT00000114834.1	Tsc2-203	6139	1635aa	ENSRNOP00000087212.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AG49	-
ENSRNOT00000016221.4	Tsc2-201	5653	1809aa	ENSRNOP00000016221.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JSL4	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data