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

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Gene: RGSL1 ENSBTAG00000018220

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Description

regulator of G protein signaling like 1 [Source:VGNC Symbol;Acc:VGNC:33928]

Location

Primary_assembly 16: 63,544,117-63,603,943 forward strand.

ARS-UCD2.0:CM008183.2

About this gene

This gene has 5 transcripts (splice variants), 115 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000102730.1	RGSL1-202	4506	1101aa	ENSBTAP00000098189.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TLT5	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,
ENSBTAT00000135522.1	RGSL1-203	4390	1065aa	ENSBTAP00000098018.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TI97	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,
ENSBTAT00000097197.1	RGSL1-204	4365	1066aa	ENSBTAP00000087275.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SPJ6	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,
ENSBTAT00000044259.5	RGSL1-201	4229	1075aa	ENSBTAP00000041768.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E1BC83	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,
ENSBTAT00000127845.1	RGSL1-205	3944	1069aa	ENSBTAP00000082494.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SIX0	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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