Summary
- Splice variants
- Transcript comparison
- Gene alleles
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- GO: Molecular function
- GO: Biological process
- GO: Cellular component
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Genetic Variation
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ID History
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Gene: Lcorl ENSRNOG00000003787

Description

ligand dependent nuclear receptor corepressor-like [Source:RGD Symbol;Acc:1561241]

Gene Synonyms

LOC498385, RGD1561241

Location

GRCr8:CM070404.1

About this gene

This gene has 2 transcripts (splice variants), 129 orthologues and is associated with 1 phenotype.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000101649.2	Lcorl-202	4727	550aa	ENSRNOP00000095424.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GLM1	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,
ENSRNOT00000100583.2	Lcorl-201	4635	514aa	ENSRNOP00000091243.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AQ15	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,

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