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: Clec2d2 ENSRNOG00000059890

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Description

C-type lectin domain family 2 member D2 [Source:RGD Symbol;Acc:1562831]

Gene Synonyms

Clr2, LOC362445, RGD1562831

Location

Primary_assembly 4: 162,059,008-162,071,088 reverse strand.

mRatBN7.2:CM026977.1

About this gene

This gene has 1 transcript (splice variant), 322 orthologues and 56 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000038801.7	Clec2d2-201	3106	233aa	ENSRNOP00000035114.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A4KWA5	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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