SH3PXD2B Products

Bioinformatics

Entrez	285590 Human
Uniprot	NP_001017995 Human
Product By Gene ID	285590
Alternate Names	SH3 and PX domains 2B

Diseases related to SH3PXD2B

Discover more about diseases related to SH3PXD2B.

Eye Abnormalities
Craniofacial Abnormalities
Irido-corneal Dysgenesis
Orbital Separation Excessive
Congenital Heart Defects
Congenital Abnormality
Intraocular Pressure Disorder
Tissue Adhesions
Glaucoma
Hydrophthalmos
Brachycephaly
Interparietal Craniosynostosis
Neoplasm Metastasis
Primary Congenital Glaucoma
Congenital Musculoskeletal Anomalies
Glaucoma, Open-angle
Otitis Media
Infertility
Dysplasia
Malignant Neoplasms

Pathways for SH3PXD2B

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Cell Migration
Regulation Of Growth
Proteolysis
Cell-matrix Adhesion
Pathogenesis
Localization

PTMs for SH3PXD2B

Learn more about PTMs related to SH3PXD2B.

Phosphorylation

Bioinformatics Tool for SH3PXD2B

Discover related pathways, diseases and genes to SH3PXD2B. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.