Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
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Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: sdpn-1 WBGene00018467

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Description

SH3 domain-containing protein [Source:NCBI gene (formerly Entrezgene);Acc:181058]

Location

Chromosome X: 7,988,931-7,998,229 reverse strand.

WBcel235:BX284606.5

About this gene

This gene has 3 transcripts (splice variants) and 821 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
F45E1.7b.1	sdpn-1-203	1488	495aa	F45E1.7b.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6AHQ8	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,
F45E1.7a.1	sdpn-1-201	1886	489aa	F45E1.7a.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q09989	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,
F45E1.7a.2	sdpn-1-202	1734	489aa	F45E1.7a.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q09989	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,

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Summary

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