Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
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ID History
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Gene: Lnp1 ENSRNOG00000039649

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Description

leukemia NUP98 fusion partner 1 [Source:RGD Symbol;Acc:2323126]

Gene Synonyms

LOC100359918

Location

Primary_assembly 11: 57,123,129-57,148,586 forward strand.

GRCr8:CM070401.1

About this gene

This gene has 2 transcripts (splice variants), 106 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000132233.1	Lnp1-202	1740	179aa	ENSRNOP00000099104.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000060802.6	Lnp1-201	1199	161aa	ENSRNOP00000057529.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M9K8	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,

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Summary

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