Summary
- Splice variants
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Sequence
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Comparative Genomics
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- Orthologues
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Phenotypes
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Gene: Ino80e ENSRNOG00000019960

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Description

INO80 complex subunit E [Source:RGD Symbol;Acc:1359572]

Gene Synonyms

CCDC95, LOC293494

Location

Primary_assembly 1: 190,891,936-190,902,541 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 179 orthologues and is associated with 12 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000027033.6	Ino80e-201	2043	244aa	ENSRNOP00000027034.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2UKE2 A6I9G3 Q6AYH2	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,
ENSRNOT00000107197.2	Ino80e-202	1759	205aa	ENSRNOP00000083835.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G9J0	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,

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data