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
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Haus2 ENSRNOG00000048933

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Description

HAUS augmin like complex subunit 2 [Source:RGD Symbol;Acc:9250626]

Gene Synonyms

LOC103691872, LOC691918

Location

Primary_assembly 3: 128,006,932-128,019,729 forward strand.

GRCr8:CM070393.1

About this gene

This gene has 1 transcript (splice variant), 184 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000076309.3	Haus2-201	940	234aa	ENSRNOP00000068058.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096MJA8 A0A8J8YP33	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,

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Summary

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