Transcript: ENST00000407684.1 GAREM2-202

Description

GRB2 associated regulator of MAPK1 subtype 2 [Source:HGNC Symbol;Acc:HGNC:27172]

Gene Synonyms

FAM59B, FLJ00375, GAREML, KIAA2038

Location

Chromosome 2: 26,180,716-26,189,644 forward strand.

About this transcript

This transcript has 6 exons, is annotated with 19 domains and features, is associated with 4170 variant alleles and maps to 332 oligo probes.

Gene

This transcript is a product of gene ENSG00000157833.13 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq Match	Flags
ENST00000401533.7	GAREM2-201	4164	874aa	ENSP00000384593.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS54336	Q75VX8-1	NM_001168241.2	The Matched Annotation from NCBI and EMBL-EBI is a collaboration between Ensembl/GENCODE and RefSeq. The MANE Select is a default transcript per human gene that is representative of biology, well-supported, expressed and highly-conserved. This transcript set matches GRCh38 and is 100% identical between RefSeq and Ensembl/GENCODE for 5' UTR, CDS, splicing and 3'UTR.MANE Select, 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,
ENST00000407684.1	GAREM2-202	5138	664aa	ENSP00000384581.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS54337	Q75VX8-3	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, TSL 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs 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:2,
ENST00000496070.1	GAREM2-203	273	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	-	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,

Summary

Statistics

Exons: 6, Coding exons: 6, Transcript length: 5,138 bps, Translation length: 664 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q75VX8

CCDS

This transcript is a member of the Human CCDS set: CCDS54337

Transcript Support Level (TSL)

TSL:2

Version

ENST00000407684.1

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

Transcript: ENST00000407684.1 GAREM2-202

Summary

About Us

Get help

Our sister sites

Follow us

Favourite species

All species

Recent locations

Transcript: ENST00000407684.1 GAREM2-202

Summary

About Us

Get help

Our sister sites

Follow us