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

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: Cep15 ENSMUSG00000033111

.

Description

centrosomal protein 15 [Source:MGI Symbol;Acc:MGI:1917937]

Gene Synonyms

3830406C13Rik

Location

Chromosome 14: 10,166,532-10,185,590 reverse strand.

GRCm39:CM001007.3

About this gene

This gene has 19 transcripts (splice variants), 153 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000223702.2	Cep15-205	900	135aa	ENSMUSP00000153330.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A286YDP6	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,
ENSMUST00000112669.10	Cep15-201	2477	90aa	ENSMUSP00000108288.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS36805	Q8BGD0-2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. 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:1,
ENSMUST00000163392.3	Cep15-202	2452	127aa	ENSMUSP00000126960.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS26817	Q8BGD0	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 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. 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:1,
ENSMUST00000224389.2	Cep15-209	2444	127aa	ENSMUSP00000153430.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS26817	Q8BGD0	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,
ENSMUST00000223762.2	Cep15-206	2292	127aa	ENSMUSP00000153287.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS26817	Q8BGD0	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,
ENSMUST00000225294.2	Cep15-213	1191	127aa	ENSMUSP00000153402.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS26817	Q8BGD0	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,
ENSMUST00000223631.2	Cep15-203	1014	90aa	ENSMUSP00000153352.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS36805	Q8BGD0-2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENSMUST00000223927.2	Cep15-207	1010	90aa	ENSMUSP00000153588.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS36805	Q8BGD0-2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENSMUST00000225847.2	Cep15-218	680	89aa	ENSMUSP00000153505.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A286YE50	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSMUST00000225640.2	Cep15-215	462	55aa	ENSMUSP00000153272.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A286YD50	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSMUST00000225773.2	Cep15-217	417	109aa	ENSMUSP00000153288.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A286YD67	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENSMUST00000225971.2	Cep15-219	809	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-
ENSMUST00000224824.2	Cep15-210	454	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-
ENSMUST00000225383.2	Cep15-214	431	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-
ENSMUST00000224994.2	Cep15-211	361	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-
ENSMUST00000225739.2	Cep15-216	336	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-
ENSMUST00000225052.2	Cep15-212	2469	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-
ENSMUST00000223697.2	Cep15-204	915	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-
ENSMUST00000224223.2	Cep15-208	615	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-

.

Strains

.

Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

.

Personal Data