Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Molecular function
- GO: Biological process
- 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: Sft2d2 ENSRNOG00000003038

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Description

SFT2 domain containing 2 [Source:RGD Symbol;Acc:1310623]

Gene Synonyms

LOC360868, RGD1310623

Location

Primary_assembly 13: 80,008,480-80,037,473 reverse strand.

GRCr8:CM070403.1

About this gene

This gene has 2 transcripts (splice variants), 245 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000076289.4	Sft2d2-202	5404	204aa	ENSRNOP00000068143.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096MJI6	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,
ENSRNOT00000004065.8	Sft2d2-201	1668	193aa	ENSRNOP00000004065.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	R9PXR9	-

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Summary

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