CYLN2 Products

Description

The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq]

Bioinformatics

Entrez	7461 Human
Uniprot	AAI48703.1 Human
Product By Gene ID	7461
Alternate Names	CAP-GLY domain containing linker protein 2 CAP-Gly domain-containing linker protein 2 CLIP CLIP-115Williams-Beuren syndrome chromosomal region 3 protein CYLN2WBSCR3 cytoplasmic linker 2 Cytoplasmic linker protein 115 KIAA0291Williams-Beuren syndrome chromosomal region 4 protein WBSCR4MGC11333 Williams-Beuren syndrome chromosome region 3 Williams-Beuren syndrome chromosome region 4 WSCR3 WSCR4Cytoplasmic linker protein 2