Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- 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: Chrdl2 ENSRNOG00000018394

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Description

chordin-like 2 [Source:RGD Symbol;Acc:1306179]

Gene Synonyms

LOC308854

Location

Primary_assembly 1: 163,755,316-163,782,757 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 118 orthologues and 21 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000101177.2	Chrdl2-202	1389	434aa	ENSRNOP00000090366.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AAN2	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,
ENSRNOT00000024803.9	Chrdl2-201	1529	429aa	ENSRNOP00000024803.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6I6L1 F1LW58	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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