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DB built by WormBase

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Gene: anoh-2 WBGene00013326

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Description

Anoctamin [Source:NCBI gene;Acc:178395]

Location

Chromosome IV: 14,658,308-14,675,155 forward strand.

WBcel235:BX284604.4

About this gene

This gene has 3 transcripts (splice variants), 63 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
-	Y57G11C.37b.1	2682	893aa	Y57G11C.37b.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2L2L3	-	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,
-	Y57G11C.37a.1	2859	837aa	Y57G11C.37a.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8I4C3	-	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,
-	Y57G11C.37a.2	2687	837aa	Y57G11C.37a.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8I4C3	-	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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