Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Gene families
Literature
Metazoan Compara
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- Gene tree (Metazoa)
- Gene tree (Protostomes)
- Gene tree (Insects)
- Gene gain/loss tree
- Orthologues
- Paralogues
Pan-taxonomic Compara
- Gene Tree
- Orthologues
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- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
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Molecular interactions
Regulation
External references
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ID History
- Gene history

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DB built by WormBase

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Gene: T19D12.2 WBGene00020577

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Description

Uncharacterized protein [Source:NCBI gene;Acc:174099]

Location

Chromosome II: 6,661,335-6,665,220 forward strand.

WBcel235:BX284602.5

About this gene

This gene has 5 transcripts (splice variants), 6 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
-	T19D12.2c.1	2730	516aa	T19D12.2c.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2L078	-	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,
-	T19D12.2a.2	2709	610aa	T19D12.2a.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2L077	-	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,
-	T19D12.2b.1	2269	422aa	T19D12.2b.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q86ND3	-	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,
-	T19D12.2a.1	2167	610aa	T19D12.2a.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2L077	-	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,
-	T19D12.2c.2	1692	516aa	T19D12.2c.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2L078	-	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,

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Summary

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