Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
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: Ccdc169 ENSRNOG00000038095

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Description

coiled-coil domain containing 169 [Source:RGD Symbol;Acc:1593170]

Gene Synonyms

LOC499618

Location

Primary_assembly 2: 139,321,670-139,351,161 forward strand.

mRatBN7.2:CM026975.1

About this gene

This gene has 3 transcripts (splice variants), 67 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000103039.1	Ccdc169-203	1863	217aa	ENSRNOP00000090646.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AE52	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,
ENSRNOT00000019018.7	Ccdc169-201	2271	214aa	ENSRNOP00000019018.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4ABE7	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,
ENSRNOT00000082923.2	Ccdc169-202	672	207aa	ENSRNOP00000072706.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K3N0	-

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Summary

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