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CEP41 encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. Additionally we are shipping CEP41 Kits (12) and CEP41 Proteins (9) and many more products for this protein.
Showing 10 out of 13 products:
Human Polyclonal CEP41 Primary Antibody for IHC, ELISA - ABIN1451148
Yamada, Kayashima, Yamasaki, Ohta, Yoshiura, Matsumoto, Fujimoto, Niikawa, Kishino: The gene TSGA14, adjacent to the imprinted gene MEST, escapes genomic imprinting. in Gene 2002
Show all 2 references for ABIN1451148
In cortices, the MEST promoter was hemimethylated, as expected for a differentially methylated imprinting control region, whereas the COPG2 and TSGA14 promoters were completely demethylated, typical for transcriptionally active non-imprinted genes.
The data identified CEP41 mutations as a cause of Joubert syndrome and implicated tubulin (show TUBB Antibodies) post-translational modification in the pathogenesis of human ciliary dysfunction.
Three rare potentially pathogenic variants were identified in the TSGA14 gene, which encodes a centrosomal protein.
This gene encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in this gene have been associated with Joubert Syndrome 15\; an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants.
centrosomal protein of 41 kDa
, testis specific gene A14
, testis-specific gene A14 protein
, testis specific, 14
, centrosomal protein 41 kDa
, testis specific protein A14
, centrosomal protein of 41 kDa A
, ribosomal protein L37a