Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
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Molecular interactions
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ID History
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Gene: NASP ENSBTAG00000015346

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Description

nuclear autoantigenic sperm protein [Source:VGNC Symbol;Acc:VGNC:31887]

Location

Primary_assembly 3: 100,460,376-100,488,636 reverse strand.

ARS-UCD2.0:CM008170.2

About this gene

This gene has 5 transcripts (splice variants) and 275 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000078061.2	NASP-202	2478	777aa	ENSBTAP00000063517.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M1D3	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,
ENSBTAT00000068707.2	NASP-201	3102	755aa	ENSBTAP00000065266.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M5Q7	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,
ENSBTAT00000020401.6	NASP-203	2286	713aa	ENSBTAP00000020401.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAF6Z1A5	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,
ENSBTAT00000117912.2	NASP-204	1551	450aa	ENSBTAP00000103089.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TXM6 A5D969	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,
ENSBTAT00000057267.4	NASP-205	1470	423aa	ENSBTAP00000048905.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6QS28	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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