Summary
- Splice variants
- Transcript comparison
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- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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Genetic Variation
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ID History
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Gene: Haus8 ENSRNOG00000052038

Description

HAUS augmin-like complex, subunit 8 [Source:RGD Symbol;Acc:1311565]

Gene Synonyms

LOC290626, MGC108884, Ny-sar-48, RGD1311565

Location

GRCr8:CM070406.1

About this gene

This gene has 2 transcripts (splice variants) and 165 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000078714.3	Haus8-201	1539	416aa	ENSRNOP00000069134.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JUK5	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000090775.3	Haus8-202	1446	385aa	ENSRNOP00000071943.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2UQJ0 Q5BK57	APPRIS ALT2: 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 appear to be conserved in fewer than 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 ALT2,

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