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: SLC11A2 ENSBTAG00000032914

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Description

solute carrier family 11 member 2 [Source:NCBI gene (formerly Entrezgene);Acc:521189]

Location

Primary_assembly 5: 28,721,754-28,754,681 forward strand.

ARS-UCD1.3:CM008172.2

About this gene

This gene has 4 transcripts (splice variants), 263 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000079221.2	SLC11A2-202	2968	642aa	ENSBTAP00000064299.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LUR6	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,
ENSBTAT00000070008.2	SLC11A2-201	4872	589aa	ENSBTAP00000059851.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LS52	-
ENSBTAT00000055494.4	SLC11A2-203	4509	562aa	ENSBTAP00000052112.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A7MBI9	-
ENSBTAT00000068742.2	SLC11A2-204	2746	568aa	ENSBTAP00000072465.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MRJ4	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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