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

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Gene: RGL1 ENSBTAG00000019630

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Description

ral guanine nucleotide dissociation stimulator like 1 [Source:VGNC Symbol;Acc:VGNC:33903]

Location

Primary_assembly 16: 64,684,384-64,961,888 forward strand.

ARS-UCD2.0:CM008183.2

About this gene

This gene has 5 transcripts (splice variants), 206 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000026153.8	RGL1-202	4879	813aa	ENSBTAP00000026153.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N644	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 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,
ENSBTAT00000076160.3	RGL1-201	5125	803aa	ENSBTAP00000068196.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1NAC7	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,
ENSBTAT00000117440.2	RGL1-203	4873	811aa	ENSBTAP00000089450.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SZD0	-
ENSBTAT00000103730.2	RGL1-205	4783	771aa	ENSBTAP00000080463.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SAJ1	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,
ENSBTAT00000127727.2	RGL1-204	4765	775aa	ENSBTAP00000077971.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9RWX4	APPRIS ALT1: 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 is conserved in at least 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 ALT1,

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Summary

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