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: C2CD2 ENSPTRG00000013932

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Description

C2 calcium dependent domain containing 2 [Source:VGNC Symbol;Acc:VGNC:14650]

Location

Chromosome 21: 28,417,093-28,485,790 reverse strand.

Pan_tro_3.0:CM004190.1

About this gene

This gene has 1 transcript (splice variant), 193 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000025986.6	C2CD2-201	6398	696aa	ENSPTRP00000023975.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WW47 H2QL21	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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