Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
External references
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ID History
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Gene: Nomo1 ENSRNOG00000021118

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Description

Nodal modulator 1 [Source:RGD Symbol;Acc:1305240]

Gene Synonyms

LOC361578, RGD1305240

Location

Primary_assembly 1: 105,641,879-105,692,707 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 209 orthologues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000028680.7	Nomo1-201	4285	1230aa	ENSRNOP00000028680.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZSA9	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 P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5,
ENSRNOT00000108370.2	Nomo1-202	4097	1174aa	ENSRNOP00000084848.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZY21	-

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Summary

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