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
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Export data

Share this page

Bookmark this page

.

Gene: Ddx19b ENSRNOG00000064019

.

Description

DEAD-box helicase 19B [Source:RGD Symbol;Acc:1593382]

Gene Synonyms

LOC690693, Zd10a

Location

Primary_assembly 19: 55,877,567-55,906,745 reverse strand.

GRCr8:CM070409.1

About this gene

This gene has 3 transcripts (splice variants), 188 orthologues and 39 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000118121.2	Ddx19b-204	6577	492aa	ENSRNOP00000083150.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GAE6	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,
ENSRNOT00000094677.2	Ddx19b-203	6345	481aa	ENSRNOP00000090537.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ADW1	-
ENSRNOT00000084462.3	Ddx19b-202	6342	480aa	ENSRNOP00000069097.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JUH2	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,

.

Paralogues

.

.

Personal Data