SNX7 Products

Description

SNX7 encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region like some family members, and its function is unknown. This gene results in two transcript variants encoding two distinct isoforms.

Bioinformatics

Entrez	51375 Human
Uniprot	NP_057060 Human Q9UNH6 Human AAH18105 Human NP_689424 Human
Product By Gene ID	51375
Alternate Names	sorting nexin-7 MGC8717 DKFZp564F052 sorting nexin 7

Diseases related to SNX7

Discover more about diseases related to SNX7.

Spastic Paraplegia, Hereditary
Posterior Reversible Encephalopathy Syndrome
Persistent Vomiting
Endometrial Polyp
Hiatal Hernia
Hernia
Malignant Neoplasms
Paraplegia
Spastic Paraplegia
Chromosomal Translocation
Loss Of Chromosome 13
Malignant Neoplasm Of Ovary
Ovarian Neoplasm
Vomiting

Pathways for SNX7

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Transport
Drug Resistance
Transposition
Endocytosis
Protein Transport
Liver Development

Research Areas for SNX7

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Signal Transduction

Bioinformatics Tool for SNX7

Discover related pathways, diseases and genes to SNX7. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.