Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: PDGFRA ENSGALG00010013621

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Description

platelet-derived growth factor receptor, alpha polypeptide [Source:NCBI gene (formerly Entrezgene);Acc:395509]

Gene Synonyms

PDGFR, PDGFR-A

Location

Primary_assembly 4: 64,913,447-64,949,864 reverse strand.

bGalGal1.mat.broiler.GRCg7b:CM028485.1

About this gene

This gene has 5 transcripts (splice variants), 203 orthologues and 53 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010032756.1	PDGFRA-204	7275	1278aa	ENSGALP00010019405.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0YKS4	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,
ENSGALT00010032722.1	PDGFRA-201	7254	1271aa	ENSGALP00010019387.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0YT48	-
ENSGALT00010032729.1	PDGFRA-202	6840	1133aa	ENSGALP00010019391.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0YEY4	-
ENSGALT00010032763.1	PDGFRA-205	6759	1106aa	ENSGALP00010019409.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0YN75	-
ENSGALT00010032740.1	PDGFRA-203	6690	1087aa	ENSGALP00010019398.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V0YLC3	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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