Gene: Fem1c ENSMUSG00000033319

Description

fem 1 homolog c [Source:MGI Symbol;Acc:MGI:2444737]

Gene Synonyms

2610312A07Rik, 3632443A22Rik

Location

GRCm39:CM001011.3

About this gene

This gene has 1 transcript (splice variant), 207 orthologues, 5 paralogues and is associated with 1 phenotype.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000036226.6	Fem1c-201	5726	617aa	ENSMUSP00000038816.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS29231	B2RRW5 Q8CEF1	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,

Summary