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: Ccdc69 ENSRNOG00000021370

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Description

coiled-coil domain containing 69 [Source:RGD Symbol;Acc:1562251]

Gene Synonyms

LOC497906, RGD1562251

Location

Primary_assembly 10: 39,673,985-39,700,579 reverse strand.

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants), 187 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000039040.6	Ccdc69-201	1529	233aa	ENSRNOP00000037400.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZTN8	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000101308.2	Ccdc69-202	1539	194aa	ENSRNOP00000094112.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AK54	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,

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Summary

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