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
External references
Supporting evidence
ID History
- Gene history

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Gene: Ly6cl1 ENSRNOG00000037375

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Description

Ly6-C antigen like 1 [Source:RGD Symbol;Acc:1565410]

Gene Synonyms

LOC503162, RGD1565410

Location

Primary_assembly 7: 109,003,347-109,008,841 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 40 orthologues and 5 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000082405.3	Ly6cl1-202	538	163aa	ENSRNOP00000084763.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0BN41	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,
ENSRNOT00000056557.6	Ly6cl1-201	566	139aa	ENSRNOP00000053396.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F7EWC5	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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Summary

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