| Type | Description |
|---|---|
| Definition | general transcription factor II I |
| Date | Results | Publications |
|---|---|---|
| 2020-05-23 11:13:00 | Gtf2i and Gtf2ird1 mutation do not account for the full phenotypic effect of the Williams syndrome critical region in mouse models | 31418010 |
| 2019-08-24 10:35:00 | Mice with a single copy of Gtf2i (Gtf2i(+/Del)) had increased axonal outgrowth and increased TRPC3-mediated calcium entry upon carbachol stimulation. | 30120731 |
| 2019-05-25 11:01:00 | Study provides molecular and cellular evidence for myelination deficits in Williams syndrome linked to neuronal deletion of Gtf2i. | 31011227 |
| 2019-02-16 10:05:00 | The results suggest a role for GTF2i in the hypersocial phenotype of WBS and more broadly in the regulation of social behavior. Support was not observed for the role of GTF2i in ASD. | 29568691 |
| 2017-02-04 12:44:00 | The Cre-mediated deletion of exon 3 recapitulates a genetic null phenotype, indicating that the conditional Gtf2i line is a valuable tool for studying TFII-I function during embryonic development | 27194223 |
| Type | IDs |
|---|---|
| Synonymous | 6030441I21Rik, BAP-135, Diws1t, GtfII-I, Spin, TFII-I, WBSCR6 |
| Gene |
UniProtKB-ID:
GTF2I_MOUSE,
Q3UHU8_MOUSE
UniprotKB:
Q9ESZ8,
Q3UHU8
UniParc:
UPI00000E761A,
UPI0000217BC7,
UPI00000E59E1,
UPI00002264BC,
UPI00005AC607,
UPI00000E7E3A,
UPI00000E6DDB
EMBL:
AK013348,
AF289666,
AF325177,
AK006796,
AK147201,
AF043219,
AY030293,
AF043220,
AY030292,
AY030291,
AY030290,
BC053044,
AC093346,
AF017085
Ensembl:
ENSMUSG00000060261
KO:
mmu:14886
|
| Nucleutide sequences |
EMBL-CDS:
AAC02991.1,
AAH53044.1,
BAB24743.1,
BAB28803.2,
AAK49786.1,
AAF99338.1,
AAK49787.1,
AAK49785.1,
AAC53569.1,
AAK49788.1,
AAC02990.1,
BAE27759.1
Ensembl_TRS:
ENSMUST00000082057,
ENSMUST00000174155,
ENSMUST00000173888,
ENSMUST00000111261,
ENSMUST00000174354,
ENSMUST00000174772,
ENSMUST00000174513,
ENSMUST00000059042,
ENSMUST00000173341
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000080714,
ENSMUSP00000049625,
ENSMUSP00000133566,
ENSMUSP00000134440,
ENSMUSP00000133489,
ENSMUSP00000106892,
ENSMUSP00000133740,
ENSMUSP00000133969,
ENSMUSP00000133444
RefSeq:
NP_001074216.1,
XP_036020704.1,
XP_036020707.1,
XP_006504452.1,
XP_036020706.1,
XP_030110015.1,
XP_030110004.1,
XP_030110000.1,
XP_036020703.1,
XP_036020695.1,
XP_030110019.1,
NP_001345993.1,
XP_030110005.1,
XP_036020702.1,
XP_036020711.1,
NP_001345991.1,
XP_030110006.1,
XP_006504448.1,
NP_001345996.1,
XP_036020701.1,
XP_030110016.1,
XP_036020697.1,
XP_030110013.1,
XP_036020699.1,
XP_030110001.1,
NP_001345994.1,
XP_030110024.1,
XP_036020698.1,
XP_017176170.1,
NP_001345995.1,
XP_030110022.1,
XP_030110008.1,
NP_001074217.1,
XP_030110011.1,
XP_006504447.1,
NP_001074218.1,
NP_001345992.1,
NP_001074215.1,
XP_030110017.1,
XP_036020696.1,
XP_030110025.1,
XP_017176166.1,
XP_036020709.1,
XP_006504454.1,
XP_036020708.1,
XP_036020712.1,
XP_030110021.1,
XP_036020700.1,
XP_036020705.1,
XP_006504449.1,
XP_030110007.1,
NP_034495.2,
XP_030110018.1,
XP_030110023.1,
XP_030110014.1,
XP_036020710.1
|
| Others |
UniRef100:
UniRef100_Q3UHU8,
UniRef100_Q9ESZ8
UniRef90:
UniRef90_Q9ESZ8-3,
UniRef90_Q9ESZ8
UniRef50:
UniRef50_Q9ESZ8
UniGene:
Mm.261570,
Mm.412191
CCDS:
CCDS39300.1,
CCDS57386.1,
CCDS39299.1,
CCDS39301.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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