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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Nell1 ENSRNOG00000015675

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Description

neural EGFL like 1 [Source:RGD Symbol;Acc:620998]

Location

Primary_assembly 1: 108,845,462-109,709,858 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 4 transcripts (splice variants), 202 orthologues, 1 paralogue and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000145487.1	Nell1-203	3388	810aa	ENSRNOP00000112278.1	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,
ENSRNOT00000149591.1	Nell1-204	3217	753aa	ENSRNOP00000106461.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000094328.2	Nell1-202	3034	763aa	ENSRNOP00000083529.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A059	-
ENSRNOT00000056030.6	Nell1-201	2931	767aa	ENSRNOP00000052883.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q62919	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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