Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Tsg101 ENSRNOG00000013381

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Description

tumor susceptibility 101 [Source:RGD Symbol;Acc:3909]

Gene Synonyms

Rw

Location

Primary_assembly 1: 106,535,021-106,578,775 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants), 134 orthologues, 1 paralogue and is associated with 10 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000018194.8	Tsg101-201	1554	422aa	ENSRNOP00000018194.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q9C5	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,
ENSRNOT00000148566.1	Tsg101-204	1568	382aa	ENSRNOP00000107951.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000097244.2	Tsg101-202	1312	355aa	ENSRNOP00000080249.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZSM6	-
ENSRNOT00000112656.2	Tsg101-203	1195	384aa	ENSRNOP00000080071.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6IRE4	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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Summary

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