Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
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Gene: Fam174a ENSMUSG00000051185

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Description

family with sequence similarity 174, member A [Source:MGI Symbol;Acc:MGI:1914948]

Gene Synonyms

2310044D20Rik, Tmem157

Location

Chromosome 1: 95,241,348-95,263,009 forward strand.

GRCm39:CM000994.3

About this gene

This gene has 2 transcripts (splice variants) and 108 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000186780.2	Fam174a-202	3460	190aa	ENSMUSP00000139943.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q9D3L0	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, 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,
ENSMUST00000059975.8	Fam174a-201	2112	190aa	ENSMUSP00000057670.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS35674	Q9D3L0	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,

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Summary

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