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
External references
Supporting evidence
ID History
- Gene history

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Gene: Mpz ENSRNOG00000003171

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Description

myelin protein zero [Source:RGD Symbol;Acc:3109]

Gene Synonyms

MPP, P0

Location

Primary_assembly 13: 86,103,290-86,109,155 forward strand.

GRCr8:CM070403.1

About this gene

This gene has 3 transcripts (splice variants), 175 orthologues, 5 paralogues and is associated with 39 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000004279.7	Mpz-201	1990	299aa	ENSRNOP00000004279.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q1P3	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,
ENSRNOT00000152564.1	Mpz-203	1951	244aa	ENSRNOP00000112447.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000109813.2	Mpz-202	1784	236aa	ENSRNOP00000095879.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GLD0	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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