Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: FOLR3 ENSSSCG00000022236

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Description

folate receptor 3 (gamma) [Source:NCBI gene (formerly Entrezgene);Acc:396784]

Location

Primary_assembly 9: 6,746,752-6,750,799 forward strand.

Sscrofa11.1:CM000820.5

About this gene

This gene has 3 transcripts (splice variants), 140 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000053637.2	FOLR3-202	1369	346aa	ENSSSCP00000057418.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BLX2 A0A4X1V387	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 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,
ENSSSCT00000026292.4	FOLR3-201	903	296aa	ENSSSCP00000022122.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1KHW7 I3LDJ1	-
ENSSSCT00000070030.2	FOLR3-203	765	250aa	ENSSSCP00000073819.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2RMJ1 A0A8D1ZIP2	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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