Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
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: Clec2d2l1 ENSRNOG00000037076

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Description

C-type lectin domain family 2 member D2 like 1 [Source:RGD Symbol;Acc:1588731]

Gene Synonyms

Clec2d3, LOC362446, LOC689757, RGD1563033

Location

Primary_assembly 4: 163,785,010-163,795,369 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 1 transcript (splice variant), 322 orthologues and 58 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000045501.7	Clec2d2l1-201	1164	279aa	ENSRNOP00000045915.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8J8YB25	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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