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

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Gene: SLC39A4 ENSBTAG00000046026

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Description

solute carrier family 39 member 4 [Source:VGNC Symbol;Acc:VGNC:34864]

Location

Primary_assembly 14: 533,906-538,402 forward strand.

ARS-UCD2.0:CM008181.2

About this gene

This gene has 3 transcripts (splice variants), 204 orthologues, 6 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000069250.3	SLC39A4-201	2528	772aa	ENSBTAP00000069690.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1NDU1	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,
ENSBTAT00000012255.8	SLC39A4-202	2171	653aa	ENSBTAP00000012255.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q1KZG0	-
ENSBTAT00000078125.3	SLC39A4-203	2075	621aa	ENSBTAP00000070426.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MM29	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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