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

Configure this page

Share this page

Bookmark this page

.

Gene: SHMT2 ENSPTRG00000005124

.

Description

serine hydroxymethyltransferase 2 [Source:VGNC Symbol;Acc:VGNC:8532]

Location

Chromosome 12: 32,593,308-32,598,908 reverse strand.

Pan_tro_3.0:CM000326.3

About this gene

This gene has 2 transcripts (splice variants), 243 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000087354.1	SHMT2-201	2534	504aa	ENSPTRP00000063004.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2Y0Q9 K7BCQ7	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,
ENSPTRT00000009416.5	SHMT2-202	2342	192aa	ENSPTRP00000008712.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8KWD0 A0A6D2XHA4	-

.

Summary

.

.