Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: GET1-SH3BGR ENSG00000285815

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Description

GET1-SH3BGR readthrough [Source:HGNC Symbol;Acc:HGNC:54635]

Location

Chromosome 21: 39,380,332-39,515,506 forward strand.

GRCh38:CM000683.2

About this gene

This gene has 2 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000647779.1	GET1-SH3BGR-201	1328	273aa	ENSP00000497977.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A3B3ITX9	-	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, 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,
ENST00000648253.1	GET1-SH3BGR-202	1925	173aa	ENSP00000497295.1	Nonsense mediated decay		A0A3B3ISE9	-	-

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Summary

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