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

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Gene: Slc38a6 ENSRNOG00000022622

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Description

solute carrier family 38, member 6 [Source:RGD Symbol;Acc:1310330]

Gene Synonyms

LOC299139, NAT-1, Snat6

Location

Primary_assembly 6: 97,723,471-97,785,791 forward strand.

GRCr8:CM070396.1

About this gene

This gene has 3 transcripts (splice variants), 212 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000029328.5	Slc38a6-201	2788	457aa	ENSRNOP00000035818.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HC57 F1LRY2	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,
ENSRNOT00000103137.2	Slc38a6-203	2770	451aa	ENSRNOP00000085669.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GD60	-
ENSRNOT00000100753.2	Slc38a6-202	507	130aa	ENSRNOP00000077661.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5XWD5	-

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Summary

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