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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Immunogen sequence: TKYGNSLLEEA RGEIRNLENV IQSQRGQIEE LEHLAEILKT QLRRKENEIE LSLLQLREQQ ATDQRSNIRD NVEMIKLHKQ LVEKSNALSA MEGKFIQLQE KQRTLRIS
Highest antigen sequence identity to the following orthologs - mouse 95%, rat 94%.
The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 and Meckel syndrome type 5. Two transcript variants encoding different isoforms have been found for this gene.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: DKFZp686C0668; Nephrocystin-8; Protein fantom; RPGR-interacting protein 1-like protein; RPGRIP1-like protein
基因别名: FTM; KIAA1005; NPHP8; RPGRIP1L
Entrez Gene ID: (Human) 23322