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
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Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
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External references
Supporting evidence
ID History
- Gene history

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Gene: Ccdc152 ENSMUSG00000091119

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Description

coiled-coil domain containing 152 [Source:MGI Symbol;Acc:MGI:3641617]

Gene Synonyms

ENSMUSG00000071814

Location

Chromosome 15: 3,309,552-3,333,008 reverse strand.

GRCm39:CM001008.3

About this gene

This gene has 3 transcripts (splice variants) and 148 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000226261.2	Ccdc152-202	1327	254aa	ENSMUSP00000153730.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS49571	E9PX14	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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,
ENSMUST00000165386.2	Ccdc152-201	798	254aa	ENSMUSP00000129305.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS49571	E9PX14	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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, TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5,
ENSMUST00000228405.2	Ccdc152-203	494	163aa	ENSMUSP00000153740.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A2I3BPP3	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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