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

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Gene: SH2D1A ENSSSCG00000012643

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Description

SH2 domain containing 1A [Source:NCBI gene (formerly Entrezgene);Acc:780420]

Location

Primary_assembly X: 101,824,367-101,849,671 forward strand.

Sscrofa11.1:CM000830.5

About this gene

This gene has 2 transcripts (splice variants), 208 orthologues and 13 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000013824.6	SH2D1A-201	2771	128aa	ENSSSCP00000013442.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1W811 F1RU61	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,
ENSSSCT00000072018.1	SH2D1A-202	613	125aa	ENSSSCP00000070869.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2R9R0 A0A8D1VSK3	-

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Summary

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