Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: Ncmap ENSRNOG00000048139

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Description

noncompact myelin associated protein [Source:RGD Symbol;Acc:1587554]

Gene Synonyms

LOC689826, Mp11

Location

Primary_assembly 5: 152,894,316-152,902,414 reverse strand.

GRCr8:CM070395.1

About this gene

This gene has 2 transcripts (splice variants) and 106 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000164661.1	Ncmap-202	569	106aa	ENSRNOP00000106060.1	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,
ENSRNOT00000073506.4	Ncmap-201	510	100aa	ENSRNOP00000064011.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IT53 F1M2Z5 M0R3T9	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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