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

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Gene: FLVCR1 ENSSSCG00000015590

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Description

FLVCR heme transporter 1 [Source:NCBI gene (formerly Entrezgene);Acc:100217398]

Location

Primary_assembly 9: 130,541,660-130,570,702 reverse strand.

Sscrofa11.1:CM000820.5

About this gene

This gene has 1 transcript (splice variant), 214 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000016983.4	FLVCR1-201	4130	559aa	ENSSSCP00000016529.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1TKR6 F1S2X6	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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