Gene: Nelfa ENSMUSG00000029111

Description

negative elongation factor complex member A, Whsc2 [Source:MGI Symbol;Acc:MGI:1346098]

Gene Synonyms

Nelf-A, Whsc2, Whsc2h

Location

Chromosome 5: 34,055,260-34,093,757 reverse strand.

GRCm39:CM000998.3

About this gene

This gene has 2 transcripts (splice variants), 201 orthologues and is associated with 11 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000030993.8	Nelfa-201	2580	530aa	ENSMUSP00000030993.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS19208	Q8BG30	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,
ENSMUST00000132942.2	Nelfa-202	1926	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	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,

Gene: Nelfa ENSMUSG00000029111

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Gene: Nelfa ENSMUSG00000029111

Summary

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