Gene: C1qtnf1 ENSMUSG00000017446

Description

C1q and tumor necrosis factor related protein 1 [Source:MGI Symbol;Acc:MGI:1919254]

Gene Synonyms

1600017K21Rik, CTRP1

Location

Chromosome 11: 118,319,029-118,340,789 forward strand.

GRCm39:CM001004.3

About this gene

This gene has 4 transcripts (splice variants), 158 orthologues, 20 paralogues and is associated with 51 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000017590.9	C1qtnf1-201	2532	281aa	ENSMUSP00000017590.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS25703	A0A3B0J1J8 Q9QXP7	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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,
ENSMUST00000106286.3	C1qtnf1-202	2512	281aa	ENSMUSP00000101893.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS25703	A0A3B0J1J8 Q9QXP7	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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,
ENSMUST00000124861.2	C1qtnf1-203	684	49aa	ENSMUSP00000122759.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A2A4W1	TSL 3: A transcript where the only support is from a single EST 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:3, 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENSMUST00000133558.3	C1qtnf1-204	246	51aa	ENSMUSP00000117467.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A2A4W2	TSL 3: A transcript where the only support is from a single EST 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:3, 3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

Gene: C1qtnf1 ENSMUSG00000017446

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Gene: C1qtnf1 ENSMUSG00000017446

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