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: SLC29A1 ENSBTAG00000015131

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Description

solute carrier family 29 member 1 [Source:VGNC Symbol;Acc:VGNC:54237]

Location

Primary_assembly 23: 17,730,856-17,741,098 forward strand.

ARS-UCD1.3:CM008190.2

About this gene

This gene has 4 transcripts (splice variants), 284 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000035955.3	SLC29A1-201	2196	535aa	ENSBTAP00000035821.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6PZI3	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,
ENSBTAT00000070658.2	SLC29A1-202	2006	499aa	ENSBTAP00000071023.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MJQ0	-
ENSBTAT00000068514.2	SLC29A1-203	1991	494aa	ENSBTAP00000070750.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q3ZC83	-
ENSBTAT00000104111.1	SLC29A1-204	1877	456aa	ENSBTAP00000102480.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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