MPZL1 Products

Description

MPZL1, or Myelin protein zero-like protein 1, contains five isoforms that are 29 kDa, 28 kDa, 23 kDa, 16 kDa, and 12 kDa, and is involved in the process of signal transduction as a cell surface receptor. Research is currently being conducted on MPZL1 and its relation to a variety of diseases and disorders, including noonan syndrome, schizophrenia, essential hypertension, t-cell leukemia, tooth disease, and choroiditis. MPZL1 has been linked to the protein tyrosine kinase signaling pathway, and has been found to interact with PTPN11, SRC, EXOSC4, UBC, and ELAVL1.

Bioinformatics

Entrez	9019 Human
Uniprot	O95297-3 Human AAH07881 Human NP_003944 Human NP_003944.1 Human NM_003953 Human
Product By Gene ID	9019
Alternate Names	protein zero related myelin protein zero-like protein 1 MPZL1b immunoglobulin family transmembrane protein Protein zero-related PZRb FLJ21047 PZRPZRa PZR1b myelin protein zero-like 1

Diseases related to MPZL1

Discover more about diseases related to MPZL1.

Charcot-marie-tooth Disease
Demyelinating Diseases
Noonan Syndrome
Polyneuropathy
Neurological Signs And Symptoms
Muscle Oedema
Adipose Tissue Atrophy
Schizophrenia
Talipes Cavus
Atrophy
Periodic Paralysis (finding)
Edema
Charcot-marie-tooth Disease, Type 2j
Corneal Diseases
Peripheral Neuropathy
Familial Periodic Paralysis
Adie Syndrome

Pathways for MPZL1

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Hyperphosphorylation
Cell Migration
Blastocyst Formation
Cell Motility
Pathogenesis

Research Areas for MPZL1

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Signal Transduction

PTMs for MPZL1

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Phosphorylation
Dephosphorylation

Bioinformatics Tool for MPZL1

Discover related pathways, diseases and genes to MPZL1. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.