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2024-04-20 22:05:55, GGRNA : RefSeq release 60 (20130726)
Summary:
Results:
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Summary: 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 .....
Synonym: BAP135; BTKAP1; DIWS; GTFII-I; IB291; SPIN; TFII-I; WBS; WBSCR6
NM_001518.3 -
Homo sapiens (human) -
NCBI -
UCSC -
RefEx発現量
Data Export:
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デバッグ用データ:
0.012 | 0.012 | q_start
0.012 | 0.000 | q_end
0.013 | 0.001 | end
by
@meso_cacase at
DBCLS
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