Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Pkd2 FBgn0041195

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Description

Polycystic kidney disease 2

Gene Synonyms

Pkd2

Location

Primary_assembly 2L: 12,398,274-12,402,023 forward strand.

BDGP6.46:AE014134.6

About this gene

This gene has 1 transcript (splice variant), 1119 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
FBtr0080365	Pkd2-RA	3271	924aa	FBpp0079947	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A223LMK5 A0A223LMN3 A0A223LMW3 A0A223LMW4 A0A223LMW5 A0A223LMY9 A0A223LN64 A0A223LND9 Q6T3S5 Q9VK95	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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