Gene: Dip2c ENSMUSG00000048264

Description

disco interacting protein 2 homolog C [Source:MGI Symbol;Acc:MGI:1920179]

Gene Synonyms

2900024P20Rik

Location

Chromosome 13: 9,326,564-9,718,964 forward strand.

GRCm39:CM001006.3

About this gene

This gene has 4 transcripts (splice variants), 292 orthologues, 2 paralogues and is associated with 21 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000166299.2	Dip2c-201	4822	1557aa	ENSMUSP00000126827.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9PWR4	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, 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,
ENSMUST00000174552.8	Dip2c-203	8023	1556aa	ENSMUSP00000133806.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS36589	B2RQ71	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,
ENSMUST00000169960.10	Dip2c-202	4801	1527aa	ENSMUSP00000131238.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		B7ZMZ7	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,
ENSMUST00000222280.2	Dip2c-204	2813	660aa	ENSMUSP00000152159.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A1Y7VMZ0	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, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

Gene: Dip2c ENSMUSG00000048264

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Gene: Dip2c ENSMUSG00000048264

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