HUMAN:MYP0

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Species (Taxon ID)	Homo sapiens (Human). (taxon:9606)
Gene Name(s)	MPZ
Protein Name(s)	Myelin protein P0 Myelin peripheral protein MPP Myelin protein zero
External Links
UniProt Identifier	MYP0_HUMAN
UniProt Accessions	P25189, Q16072, Q5VTH4, Q92677, Q9BR67,
EMBL	D10537, D14720, L24893, L24894, AK313555, BT006765, AL592295, CH471121, BC006491, S66705, U10018, U10017,
PIR	JH0252,
RefSeq	NP_000521.2,
PDB	1N2P,
IntAct	P25189,
Ensembl	ENST00000360451,
Pfam	PF10570, PF07686,

Annotations

Qualifier	GO ID	GO term name	Reference	Evidence Code	with/from	Aspect
	GO:0005198	structural molecule activity	PMID:7693129^[1]	NAS: Non-traceable Author Statement		F
	GO:0005886	plasma membrane	PMID:7693130^[2]	NAS: Non-traceable Author Statement		C
	GO:0005887	integral to plasma membrane	PMID:7506095^[3]	TAS: Traceable Author Statement		C
	GO:0007268	synaptic transmission	PMID:7693129^[1]	TAS: Traceable Author Statement		P
	GO:0016020	membrane	GO_REF:0000002	IEA: Inferred from Electronic Annotation	InterPro:IPR000920	C
	GO:0016020	membrane	GO_REF:0000004	IEA: Inferred from Electronic Annotation	SP_KW:KW-0472	C
	GO:0016020	membrane	GO_REF:0000023	IEA: Inferred from Electronic Annotation	SP_SL:SL-0162	C
	GO:0016021	integral to membrane	GO_REF:0000004	IEA: Inferred from Electronic Annotation	SP_KW:KW-0812	C
	GO:0045217	cell-cell junction maintenance	GO_REF:0000019	IEA: Inferred from Electronic Annotation	Ensembl:ENSMUSP00000066701	P
	GO:0005198	structural molecule activity	PMID:7693129^[1]	NAS: Non-traceable Author Statement		F
	GO:0005886	plasma membrane	PMID:7693130^[2]	NAS: Non-traceable Author Statement		C
	GO:0005887	integral to plasma membrane	PMID:7506095^[3]	TAS: Traceable Author Statement		C
	GO:0007268	synaptic transmission	PMID:7693129^[1]	TAS: Traceable Author Statement		P
	GO:0016020	membrane	GO_REF:0000002	IEA: Inferred from Electronic Annotation	InterPro:IPR000920	C
	GO:0016020	membrane	GO_REF:0000004	IEA: Inferred from Electronic Annotation	SP_KW:KW-0472	C
	GO:0016020	membrane	GO_REF:0000023	IEA: Inferred from Electronic Annotation	SP_SL:SL-0162	C
	GO:0016021	integral to membrane	GO_REF:0000004	IEA: Inferred from Electronic Annotation	SP_KW:KW-0812	C
	GO:0045217	cell-cell junction maintenance	GO_REF:0000019	IEA: Inferred from Electronic Annotation	Ensembl:ENSMUSP00000066701	P
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Notes

References

See Help:References for how to manage references in GONUTS.

↑ ^1.0 ^1.1 ^1.2 ^1.3 Hayasaka K et al. (1993) Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene. Nat Genet 5: 31-4 PubMed GONUTS page
↑ ^2.0 ^2.1 Kulkens T et al. (1993) Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B. Nat Genet 5: 35-9 PubMed GONUTS page
↑ ^3.0 ^3.1 Hayasaka K et al. (1993) De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III). Nat Genet 5: 266-8 PubMed GONUTS page

[PMID:7693129-0] 1.0 ^1.1 ^1.2 ^1.3 Hayasaka K et al. (1993) Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene. Nat Genet 5: 31-4 PubMed GONUTS page

[PMID:7693130-1] 2.0 ^2.1 Kulkens T et al. (1993) Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B. Nat Genet 5: 35-9 PubMed GONUTS page

[PMID:7506095-2] 3.0 ^3.1 Hayasaka K et al. (1993) De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III). Nat Genet 5: 266-8 PubMed GONUTS page

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HUMAN:MYP0

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