Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Clec2g ENSRNOG00000059538

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Description

C-type lectin domain family 2, member G [Source:RGD Symbol;Acc:1563148]

Gene Synonyms

CLEC2D11, Clr-b, Clr11, Clrb, LOC362447, RGD1563148

Location

Primary_assembly 4: 162,617,790-162,627,699 forward strand.

mRatBN7.2:CM026977.1

About this gene

This gene has 3 transcripts (splice variants), 204 orthologues and 56 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000090939.2	Clec2g-202	1024	218aa	ENSRNOP00000070591.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2R3H7	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,
ENSRNOT00000097113.1	Clec2g-203	6753	193aa	ENSRNOP00000080845.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZQN8	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,
ENSRNOT00000083188.2	Clec2g-201	1762	203aa	ENSRNOP00000069630.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JVV1	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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