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

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Gene: Dennd2b ENSRNOG00000013934

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Description

DENN domain containing 2B [Source:RGD Symbol;Acc:1308995]

Gene Synonyms

LOC102554209, LOC308944, St5

Location

Primary_assembly 1: 172,978,895-173,129,810 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 6 transcripts (splice variants), 211 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000099927.2	Dennd2b-202	4532	1215aa	ENSRNOP00000089151.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AKA1	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,
ENSRNOT00000064902.4	Dennd2b-201	4479	1146aa	ENSRNOP00000061141.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A9H6	-
ENSRNOT00000114796.2	Dennd2b-206	4292	1120aa	ENSRNOP00000085739.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A484	-
ENSRNOT00000100159.2	Dennd2b-203	4243	1134aa	ENSRNOP00000094375.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GL52	-
ENSRNOT00000100789.2	Dennd2b-204	4027	1062aa	ENSRNOP00000078383.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZM26	-
ENSRNOT00000114792.2	Dennd2b-205	3038	717aa	ENSRNOP00000093299.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AH99	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,

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Summary

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