Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: DNM2 ENSBTAG00000013362

.

Description

dynamin 2 [Source:VGNC Symbol;Acc:VGNC:28143]

Location

Primary_assembly 7: 15,209,073-15,299,499 forward strand.

ARS-UCD2.0:CM008174.2

About this gene

This gene has 6 transcripts (splice variants), 310 orthologues and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000154071.1	DNM2-203	3789	869aa	ENSBTAP00000105043.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSBTAT00000139744.1	DNM2-204	3762	860aa	ENSBTAP00000104208.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000146939.1	DNM2-205	3667	865aa	ENSBTAP00000105413.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,
ENSBTAT00000147968.1	DNM2-202	3626	869aa	ENSBTAP00000104699.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
ENSBTAT00000036123.6	DNM2-206	3461	827aa	ENSBTAP00000035986.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MW91	-
ENSBTAT00000139992.1	DNM2-201	2756	855aa	ENSBTAP00000107539.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

.

Summary

.

.