Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: NIPSNAP2 ENSPTRG00000019204

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Description

nipsnap homolog 2 [Source:VGNC Symbol;Acc:VGNC:7383]

Gene Synonyms

GBAS

Location

Chromosome 7: 55,406,013-55,442,079 forward strand.

Pan_tro_3.0:CM000321.4

About this gene

This gene has 3 transcripts (splice variants), 274 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000099937.1	NIPSNAP2-201	2410	286aa	ENSPTRP00000085452.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3S6C3 A0A6D2XNG2	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,
ENSPTRT00000035493.4	NIPSNAP2-202	1892	247aa	ENSPTRP00000032817.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WQ38 H2QUL7	-
ENSPTRT00000106798.1	NIPSNAP2-203	438	145aa	ENSPTRP00000076200.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SGN5 A0A6D2WUM5	-

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Summary

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