Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
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

Configure this page

Share this page

Bookmark this page

.

Gene: Ino80d ENSRNOG00000024272

.

Description

INO80 complex subunit D [Source:RGD Symbol;Acc:1304808]

Gene Synonyms

LOC316440, RGD1304808

Location

Primary_assembly 9: 71,951,031-72,040,232 reverse strand.

GRCr8:CM070399.1

About this gene

This gene has 2 transcripts (splice variants), 206 orthologues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000035879.8	Ino80d-201	3275	1021aa	ENSRNOP00000037428.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZTM2	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 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,
ENSRNOT00000148720.1	Ino80d-202	3065	951aa	ENSRNOP00000104757.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

.

Summary

.

.