Transcript: ENSMUST00000048718.4 Mmaa-201

Description

methylmalonic aciduria (cobalamin deficiency) type A [Source:MGI Symbol;Acc:MGI:1923805]

Gene Synonyms

2810018E08Rik

Location

Chromosome 8: 79,990,227-80,021,566 reverse strand.

About this transcript

This transcript has 7 exons, is annotated with 11 domains and features, is associated with 1707 variant alleles and maps to 188 oligo probes.

Gene

This transcript is a product of gene ENSMUSG00000037022.4 Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000048718.4	Mmaa-201	5650	415aa	ENSMUSP00000048826.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS22436	Q8C7H1	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,
ENSMUST00000210231.2	Mmaa-202	1685	155aa	ENSMUSP00000147987.2	Nonsense mediated decay		A0A1B0GSL6	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

Statistics

Exons: 7, Coding exons: 6, Transcript length: 5,650 bps, Translation length: 415 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8C7H1

CCDS

This transcript is a member of the Mouse CCDS set: CCDS22436

Transcript Support Level (TSL)

TSL:1

Version

ENSMUST00000048718.4

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.

GENCODE primary gene

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

Transcript: ENSMUST00000048718.4 Mmaa-201

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Transcript: ENSMUST00000048718.4 Mmaa-201

Summary

About Us

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