Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: CHRD ENSSSCG00000025270

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Description

chordin [Source:VGNC Symbol;Acc:VGNC:86661]

Location

Primary_assembly 13: 122,266,626-122,277,645 forward strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 2 transcripts (splice variants), 104 orthologues and 21 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000022487.4	CHRD-201	4166	957aa	ENSSSCP00000023322.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3LGX8	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,
ENSSSCT00000041472.3	CHRD-202	4046	917aa	ENSSSCP00000051552.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287B4Z3 A0A4X1UMI8	-

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Summary

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