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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: EMCCFCFDVL YCHLYGYQQP RTPRFTNEPY PLFVTWKIGR DKRLRGCIGT FSAMNLHSGL REYTLTSALK DSRFPPMTRD ELPRLFCSVS LLTNFEDVCD YLDWEVGVHG IRIEFINEKG SKRTATYLPE VAKEQGWDHI QTIDSLLRKG GYKAPITNEF RKTIKLTRYR SEKMT
Highest antigen sequence indentity to the following orthologs: Rat - 100%, Mouse - 100%.
The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced 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: AMME syndrome candidate gene 1 protein; Nuclear protein AMMECR1
基因别名: AMMECR1
Entrez Gene ID: (Human) 9949