GGRNA Home | Help | Advanced search

2024-03-29 15:21:34, 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:

Tab-delimited text. You can copy-paste the result into spreadsheet softwares (e.g., Excel, Numbers, Google Docs) or text editors.

Debug Info:

0.012 | 0.012 | q_start
0.012 | 0.000 | q_end
0.013 | 0.001 | end

by @meso_cacase at DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.