Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: SLC7A11 ENSPTRG00000016446

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Description

solute carrier family 7 member 11 [Source:VGNC Symbol;Acc:VGNC:50362]

Location

Chromosome 4: 141,477,449-141,588,488 reverse strand.

Pan_tro_3.0:CM000318.3

About this gene

This gene has 2 transcripts (splice variants), 287 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000084420.1	SLC7A11-202	1727	515aa	ENSPTRP00000068169.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RTW4	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,
ENSPTRT00000030575.4	SLC7A11-201	2227	501aa	ENSPTRP00000028239.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2VTE3 H2QQ63	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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