Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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Gene: Gpatch11 ENSRNOG00000025317

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Description

G patch domain containing 11 [Source:RGD Symbol;Acc:1311424]

Gene Synonyms

Ccdc75, LOC362685, RGD1311424

Location

Primary_assembly 6: 21,985,202-21,995,381 reverse strand.

GRCr8:CM070396.1

About this gene

This gene has 1 transcript (splice variant) and 205 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000034919.7	Gpatch11-201	1647	264aa	ENSRNOP00000031805.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LV52	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,

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Summary

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