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Summary
- Splice variants
- Transcript comparison
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Sequence
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DB built by WormBase

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Gene: pam-1 WBGene00003914

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Description

Puromycin-sensitive aminopeptidase [Source:NCBI gene;Acc:177528]

Location

Chromosome IV: 7,543,976-7,550,812 reverse strand.

WBcel235:BX284604.4

About this gene

This gene has 4 transcripts (splice variants), 95 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Name	Transcript ID	bp	Protein	Translation ID	Biotype	UniProt	RefSeq	Flags
-	F49E8.3b.1	2847	948aa	F49E8.3b.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q4TT88	-	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,
-	F49E8.3a.2	3008	884aa	F49E8.3a.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q4TT88	-	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,
-	F49E8.3a.3	2967	884aa	F49E8.3a.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q4TT88	-	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,
-	F49E8.3a.1	2812	884aa	F49E8.3a.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q4TT88	-	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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