Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SLC39A9 ENSSSCG00000028600

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Description

solute carrier family 39 member 9 [Source:VGNC Symbol;Acc:VGNC:93110]

Location

Primary_assembly 7: 93,084,336-93,143,168 forward strand.

Sscrofa11.1:CM000818.5

About this gene

This gene has 3 transcripts (splice variants) and 206 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000054220.3	SLC39A9-201	4704	328aa	ENSSSCP00000035119.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZTY0	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,
ENSSSCT00000074491.2	SLC39A9-203	5337	279aa	ENSSSCP00000066423.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QNE7	-
ENSSSCT00000025028.3	SLC39A9-202	5192	284aa	ENSSSCP00000019858.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1U4U4 I3L754	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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Breeds

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data