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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.
This gene encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11. 23. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7, 13 and 21.
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: BAP-135; Bruton tyrosine kinase-associated protein 135; BTK-associated protein 135; General transcription factor II-I; GTFII-I; OTTHUMP00000209509; SPIN; SRF-Phox1-interacting protein; TFII-I; tfiii; Williams-Beuren syndrome chromosomal region 6 protein
基因别名: 6030441I21Rik; BAP-135; BAP135; Diws1t; GTF2I; Gtf2ird1; GtfII-I; Spin; TFII-I; WBSCR6
UniProt ID: (Rat) Q5U2Y1, (Mouse) Q9ESZ8
Entrez Gene ID: (Rat) 353256, (Mouse) 14886