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2017-06-23 09:09:43, GGRNA : RefSeq release 60 (20130726)

Summary:

search term:hits:results:
refid:NM_0015181 NM_001518
[AND] 1 NM_001518

Results:

Matches are highlighted with green background. Overlapping matches are dark colored.

Homo sapiens general transcription factor IIi (GTF2I), transcript variant 4, mRNA. (4406 bp)
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 - Reference Expression

Data Export:

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Debug Info:

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by @meso_cacase at DBCLS
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