Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: prtgb ENSDARG00000040442

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Description

protogenin homolog b (Gallus gallus) [Source:NCBI gene;Acc:572241]

Gene Synonyms

prtg

Location

Chromosome 25: 418,932-463,592 forward strand.

GRCz11:CM002909.2

About this gene

This gene has 2 transcripts (splice variants), 197 orthologues and 86 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000059193.5	prtgb-201	4248	968aa	ENSDARP00000059192.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QXD0	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,
ENSDART00000154895.2	prtgb-202	446	149aa	ENSDARP00000129630.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	X1WHB8	5' and 3' truncations in transcript evidence prevent annotation of the start and the end of the CDS.CDS 5' and 3' incomplete,

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Summary

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