Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: LNP1 ENSBTAG00000034442

.

Description

leukemia NUP98 fusion partner 1 [Source:NCBI gene (formerly Entrezgene);Acc:507217]

Location

Primary_assembly 1: 44,688,511-44,730,470 forward strand.

ARS-UCD1.3:CM008168.2

About this gene

This gene has 5 transcripts (splice variants), 99 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000123733.1	LNP1-203	3163	200aa	ENSBTAP00000076699.1	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,
ENSBTAT00000135908.1	LNP1-201	3414	197aa	ENSBTAP00000098577.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000116552.1	LNP1-205	3083	186aa	ENSBTAP00000097506.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000090849.1	LNP1-204	2960	173aa	ENSBTAP00000101940.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000085137.1	LNP1-202	1968	179aa	ENSBTAP00000069436.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MJS4	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,

.

Summary

.

.