Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: mybl2a ENSDARG00000095241

.

Description

v-myb avian myeloblastosis viral onco homolog-like 2a [Source:NCBI gene (formerly Entrezgene);Acc:100005189]

Location

Chromosome 23: 4,348,265-4,357,768 forward strand.

GRCz11:CM002907.2

About this gene

This gene has 3 transcripts (splice variants), 144 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000136287.2	mybl2a-201	2810	802aa	ENSDARP00000115602.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E9QFU4	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, APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSDART00000182425.1	mybl2a-202	2421	806aa	ENSDARP00000151403.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as the principal variant. 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 P4,
ENSDART00000190593.1	mybl2a-203	2382	771aa	ENSDARP00000145018.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

.

Summary

.

.