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

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Gene: Sh2b2 ENSRNOG00000001425

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Description

SH2B adaptor protein 2 [Source:RGD Symbol;Acc:69284]

Gene Synonyms

Aps

Location

Primary_assembly 12: 26,064,486-26,093,467 forward strand.

GRCr8:CM070402.1

About this gene

This gene has 3 transcripts (splice variants), 216 orthologues, 2 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000102136.2	Sh2b2-203	2727	655aa	ENSRNOP00000097265.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GLZ7	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000001935.7	Sh2b2-201	2858	621aa	ENSRNOP00000001935.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J076 Q9Z200	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000093990.2	Sh2b2-202	1572	418aa	ENSRNOP00000095058.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GLF9	-

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data