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
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Slc35f2 ENSRNOG00000009014

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Description

solute carrier family 35, member F2 [Source:RGD Symbol;Acc:1311242]

Gene Synonyms

LOC300713

Location

Primary_assembly 8: 63,056,105-63,099,789 forward strand.

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants), 275 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000080227.3	Slc35f2-202	2658	375aa	ENSRNOP00000068904.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JTZ7	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,
ENSRNOT00000066222.3	Slc35f2-201	2455	215aa	ENSRNOP00000059061.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J4K0 D4A9C2	-

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Summary

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