Incidental Mutation 'IGL02869:Gtf2i'
| ID |
362509 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Gtf2i
|
| Ensembl Gene |
ENSMUSG00000060261 |
| Gene Name |
general transcription factor II I |
| Synonyms |
6030441I21Rik, TFII-I, BAP-135 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL02869
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
5 |
| Chromosomal Location |
134266688-134343614 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
A to G
at 134308281 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000133740
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000059042]
[ENSMUST00000082057]
[ENSMUST00000111261]
[ENSMUST00000172715]
[ENSMUST00000173341]
[ENSMUST00000174354]
[ENSMUST00000174513]
[ENSMUST00000173888]
[ENSMUST00000174155]
[ENSMUST00000174772]
|
| AlphaFold |
Q9ESZ8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000059042
|
| SMART Domains |
Protein: ENSMUSP00000049625
Gene: ENSMUSG00000060261
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
82 |
94 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
112 |
187 |
1.4e-34 |
PFAM |
|
low complexity region
|
328 |
338 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
361 |
436 |
3.4e-33 |
PFAM |
|
Pfam:GTF2I
|
466 |
541 |
5e-34 |
PFAM |
|
Pfam:GTF2I
|
571 |
646 |
3.3e-33 |
PFAM |
|
Pfam:GTF2I
|
733 |
808 |
3.9e-33 |
PFAM |
|
Pfam:GTF2I
|
868 |
943 |
9.4e-30 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000082057
|
| SMART Domains |
Protein: ENSMUSP00000080714
Gene: ENSMUSG00000060261
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
82 |
94 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
112 |
187 |
1.3e-34 |
PFAM |
|
low complexity region
|
307 |
317 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
340 |
415 |
3.3e-33 |
PFAM |
|
Pfam:GTF2I
|
445 |
520 |
4.9e-34 |
PFAM |
|
Pfam:GTF2I
|
550 |
625 |
3.2e-33 |
PFAM |
|
Pfam:GTF2I
|
712 |
787 |
3.8e-33 |
PFAM |
|
Pfam:GTF2I
|
847 |
922 |
9.1e-30 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000111261
|
| SMART Domains |
Protein: ENSMUSP00000106892
Gene: ENSMUSG00000060261
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
82 |
94 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
112 |
187 |
1.3e-34 |
PFAM |
|
low complexity region
|
309 |
319 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
342 |
417 |
3.3e-33 |
PFAM |
|
Pfam:GTF2I
|
447 |
522 |
4.9e-34 |
PFAM |
|
Pfam:GTF2I
|
552 |
627 |
3.2e-33 |
PFAM |
|
Pfam:GTF2I
|
714 |
789 |
3.8e-33 |
PFAM |
|
Pfam:GTF2I
|
849 |
924 |
9.1e-30 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000172715
|
| SMART Domains |
Protein: ENSMUSP00000134035
Gene: ENSMUSG00000060261
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
82 |
94 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
112 |
187 |
9.7e-35 |
PFAM |
|
low complexity region
|
243 |
253 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
276 |
351 |
2.4e-33 |
PFAM |
|
Pfam:GTF2I
|
381 |
456 |
3.6e-34 |
PFAM |
|
Pfam:GTF2I
|
486 |
561 |
2.4e-33 |
PFAM |
|
Pfam:GTF2I
|
648 |
723 |
2.8e-33 |
PFAM |
|
Pfam:GTF2I
|
783 |
858 |
6.7e-30 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000172904
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173341
|
| SMART Domains |
Protein: ENSMUSP00000133444
Gene: ENSMUSG00000060261
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
82 |
94 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
112 |
187 |
1e-34 |
PFAM |
|
low complexity region
|
288 |
298 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
321 |
396 |
2.6e-33 |
PFAM |
|
Pfam:GTF2I
|
426 |
501 |
3.8e-34 |
PFAM |
|
Pfam:GTF2I
|
531 |
606 |
2.5e-33 |
PFAM |
|
Pfam:GTF2I
|
693 |
768 |
3e-33 |
PFAM |
|
Pfam:GTF2I
|
832 |
907 |
7.1e-30 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000173887
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174354
|
| SMART Domains |
Protein: ENSMUSP00000134440
Gene: ENSMUSG00000060261
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
82 |
94 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
112 |
187 |
1.3e-34 |
PFAM |
|
low complexity region
|
309 |
319 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
342 |
417 |
3.3e-33 |
PFAM |
|
Pfam:GTF2I
|
447 |
522 |
4.9e-34 |
PFAM |
|
Pfam:GTF2I
|
552 |
627 |
3.2e-33 |
PFAM |
|
Pfam:GTF2I
|
714 |
789 |
3.8e-33 |
PFAM |
|
Pfam:GTF2I
|
849 |
924 |
9.1e-30 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174513
|
| SMART Domains |
Protein: ENSMUSP00000133489
Gene: ENSMUSG00000060261
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
82 |
94 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
112 |
187 |
1.3e-34 |
PFAM |
|
low complexity region
|
288 |
298 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
321 |
396 |
3.2e-33 |
PFAM |
|
Pfam:GTF2I
|
426 |
501 |
4.8e-34 |
PFAM |
|
Pfam:GTF2I
|
531 |
606 |
3.2e-33 |
PFAM |
|
Pfam:GTF2I
|
693 |
768 |
3.7e-33 |
PFAM |
|
Pfam:GTF2I
|
828 |
903 |
8.9e-30 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173888
|
| SMART Domains |
Protein: ENSMUSP00000133969
Gene: ENSMUSG00000060261
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
82 |
94 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
112 |
187 |
1.3e-34 |
PFAM |
|
low complexity region
|
245 |
258 |
N/A |
INTRINSIC |
|
low complexity region
|
269 |
279 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
302 |
377 |
3.2e-33 |
PFAM |
|
Pfam:GTF2I
|
407 |
482 |
4.6e-34 |
PFAM |
|
Pfam:GTF2I
|
512 |
587 |
3.1e-33 |
PFAM |
|
Pfam:GTF2I
|
674 |
749 |
3.6e-33 |
PFAM |
|
Pfam:GTF2I
|
809 |
884 |
8.7e-30 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174155
|
| SMART Domains |
Protein: ENSMUSP00000133566
Gene: ENSMUSG00000060261
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
82 |
94 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
112 |
186 |
1.6e-34 |
PFAM |
|
low complexity region
|
328 |
338 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
361 |
435 |
3e-33 |
PFAM |
|
Pfam:GTF2I
|
466 |
540 |
9.1e-34 |
PFAM |
|
Pfam:GTF2I
|
571 |
645 |
1.8e-32 |
PFAM |
|
Pfam:GTF2I
|
733 |
807 |
2.2e-33 |
PFAM |
|
Pfam:GTF2I
|
868 |
942 |
6e-27 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174772
|
| SMART Domains |
Protein: ENSMUSP00000133740
Gene: ENSMUSG00000060261
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
82 |
94 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
112 |
187 |
1.3e-34 |
PFAM |
|
low complexity region
|
307 |
317 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
340 |
415 |
3.3e-33 |
PFAM |
|
Pfam:GTF2I
|
445 |
520 |
4.9e-34 |
PFAM |
|
Pfam:GTF2I
|
550 |
625 |
3.2e-33 |
PFAM |
|
Pfam:GTF2I
|
712 |
787 |
3.8e-33 |
PFAM |
|
Pfam:GTF2I
|
847 |
922 |
9.1e-30 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174133
|
| SMART Domains |
Protein: ENSMUSP00000134111
Gene: ENSMUSG00000060261
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
66 |
78 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
96 |
170 |
2.7e-32 |
PFAM |
|
low complexity region
|
209 |
225 |
N/A |
INTRINSIC |
|
low complexity region
|
246 |
256 |
N/A |
INTRINSIC |
|
Pfam:GTF2I
|
279 |
353 |
5.1e-31 |
PFAM |
|
Pfam:GTF2I
|
384 |
437 |
2.7e-21 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a phosphoprotein containing six characteristic repeat motifs. The encoded protein binds to the initiator element (Inr) and E-box element in promoters and functions as a regulator of transcription. This locus, along with several other neighboring genes, is deleted in Williams-Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2013]
PHENOTYPE: Homozygotes for null allele is embryonic lethal, and show brain hemorrhage and neural tube defects. Although most heterozygote are normal and fertile, at low frequency, growth retardation and small head are also reported. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 95 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930562C15Rik |
T |
A |
16: 4,685,323 (GRCm39) |
S1142T |
possibly damaging |
Het |
| Aadacl4fm5 |
T |
C |
4: 144,512,938 (GRCm39) |
I54V |
probably benign |
Het |
| Actr3b |
T |
G |
5: 26,037,433 (GRCm39) |
V215G |
probably damaging |
Het |
| Adam9 |
C |
T |
8: 25,460,634 (GRCm39) |
V617M |
probably damaging |
Het |
| Adgrl2 |
G |
T |
3: 148,596,241 (GRCm39) |
P32T |
probably damaging |
Het |
| Afg2a |
G |
T |
3: 37,518,694 (GRCm39) |
G743W |
probably damaging |
Het |
| Ago3 |
A |
T |
4: 126,261,580 (GRCm39) |
|
probably benign |
Het |
| Allc |
A |
C |
12: 28,623,206 (GRCm39) |
I20M |
probably benign |
Het |
| Asic3 |
G |
A |
5: 24,621,972 (GRCm39) |
W361* |
probably null |
Het |
| Atf7ip |
A |
G |
6: 136,583,577 (GRCm39) |
K1203E |
probably damaging |
Het |
| Babam2 |
C |
A |
5: 32,162,116 (GRCm39) |
H272Q |
possibly damaging |
Het |
| Baz2b |
G |
A |
2: 59,807,872 (GRCm39) |
T129I |
probably benign |
Het |
| C130073F10Rik |
A |
T |
4: 101,747,590 (GRCm39) |
Y146* |
probably null |
Het |
| Cd247 |
A |
G |
1: 165,684,986 (GRCm39) |
E74G |
probably damaging |
Het |
| Cdh17 |
A |
T |
4: 11,814,908 (GRCm39) |
Q778L |
probably benign |
Het |
| Ceacam1 |
T |
C |
7: 25,175,966 (GRCm39) |
D76G |
probably benign |
Het |
| Cela3a |
T |
C |
4: 137,131,145 (GRCm39) |
K198E |
probably benign |
Het |
| Cemip2 |
T |
A |
19: 21,789,241 (GRCm39) |
D558E |
probably damaging |
Het |
| Ces2a |
T |
A |
8: 105,465,691 (GRCm39) |
D281E |
probably damaging |
Het |
| Cetn2 |
A |
T |
X: 71,958,527 (GRCm39) |
D116E |
probably damaging |
Het |
| Cracd |
A |
G |
5: 77,006,890 (GRCm39) |
K1084E |
unknown |
Het |
| Ctu2 |
G |
T |
8: 123,205,530 (GRCm39) |
|
probably null |
Het |
| Cybb |
T |
C |
X: 9,308,828 (GRCm39) |
N469D |
probably benign |
Het |
| Cygb |
C |
T |
11: 116,540,749 (GRCm39) |
R79Q |
probably damaging |
Het |
| Cyp2d10 |
C |
T |
15: 82,288,069 (GRCm39) |
V186M |
possibly damaging |
Het |
| Defb29 |
T |
A |
2: 152,380,942 (GRCm39) |
|
probably null |
Het |
| Depdc7 |
T |
G |
2: 104,560,694 (GRCm39) |
Q100P |
probably damaging |
Het |
| Dhx30 |
A |
C |
9: 109,926,251 (GRCm39) |
I91R |
probably damaging |
Het |
| Dnm1l |
T |
A |
16: 16,159,288 (GRCm39) |
K105* |
probably null |
Het |
| Eddm13 |
T |
C |
7: 6,272,898 (GRCm39) |
|
probably benign |
Het |
| Efhc1 |
T |
C |
1: 21,037,567 (GRCm39) |
I248T |
probably damaging |
Het |
| Elapor1 |
A |
G |
3: 108,380,182 (GRCm39) |
I309T |
probably benign |
Het |
| Entpd2 |
A |
G |
2: 25,288,120 (GRCm39) |
T115A |
probably damaging |
Het |
| Epb42 |
G |
T |
2: 120,856,227 (GRCm39) |
A439E |
probably benign |
Het |
| Esm1 |
T |
G |
13: 113,346,618 (GRCm39) |
L81R |
probably damaging |
Het |
| F8 |
T |
C |
X: 74,330,987 (GRCm39) |
S968G |
probably benign |
Het |
| Fam234b |
T |
G |
6: 135,202,201 (GRCm39) |
Y308D |
probably damaging |
Het |
| Fbxo46 |
T |
G |
7: 18,871,139 (GRCm39) |
V586G |
probably damaging |
Het |
| Foxp1 |
C |
A |
6: 98,907,044 (GRCm39) |
|
probably benign |
Het |
| Gm10754 |
A |
T |
10: 97,518,136 (GRCm39) |
|
probably benign |
Het |
| Gm12695 |
A |
C |
4: 96,650,370 (GRCm39) |
|
probably benign |
Het |
| Gm5468 |
T |
C |
15: 25,414,726 (GRCm39) |
|
probably benign |
Het |
| Grhl1 |
T |
C |
12: 24,631,490 (GRCm39) |
S66P |
probably damaging |
Het |
| Gstt3 |
A |
T |
10: 75,612,576 (GRCm39) |
|
probably null |
Het |
| Gzmk |
C |
A |
13: 113,308,560 (GRCm39) |
G175C |
probably damaging |
Het |
| Helz2 |
T |
C |
2: 180,872,939 (GRCm39) |
|
probably benign |
Het |
| Ift20 |
T |
C |
11: 78,430,780 (GRCm39) |
|
probably benign |
Het |
| Intu |
A |
G |
3: 40,642,216 (GRCm39) |
D491G |
probably damaging |
Het |
| Itch |
G |
T |
2: 155,015,853 (GRCm39) |
|
probably null |
Het |
| Itgb5 |
A |
G |
16: 33,665,362 (GRCm39) |
N26S |
possibly damaging |
Het |
| Lama2 |
A |
T |
10: 26,891,534 (GRCm39) |
S2526R |
probably damaging |
Het |
| Lat2 |
A |
G |
5: 134,637,027 (GRCm39) |
I40T |
probably damaging |
Het |
| Lipa |
T |
A |
19: 34,471,397 (GRCm39) |
M393L |
probably benign |
Het |
| Lipa |
G |
T |
19: 34,471,371 (GRCm39) |
|
probably benign |
Het |
| Lpcat1 |
T |
A |
13: 73,632,417 (GRCm39) |
L10H |
probably damaging |
Het |
| Lpcat3 |
T |
C |
6: 124,679,970 (GRCm39) |
Y348H |
possibly damaging |
Het |
| Lrp1b |
A |
T |
2: 40,591,842 (GRCm39) |
N50K |
unknown |
Het |
| Lrrk2 |
T |
A |
15: 91,634,480 (GRCm39) |
Y1415N |
probably damaging |
Het |
| Lsamp |
A |
T |
16: 41,965,078 (GRCm39) |
T312S |
probably benign |
Het |
| Man2a2 |
T |
C |
7: 80,013,689 (GRCm39) |
E454G |
probably benign |
Het |
| Mcm3 |
T |
C |
1: 20,879,063 (GRCm39) |
K570R |
probably damaging |
Het |
| Mctp2 |
C |
A |
7: 71,878,219 (GRCm39) |
|
probably null |
Het |
| Msantd2 |
T |
G |
9: 37,434,796 (GRCm39) |
C345W |
probably damaging |
Het |
| Musk |
T |
C |
4: 58,354,078 (GRCm39) |
I362T |
probably benign |
Het |
| Myh15 |
A |
T |
16: 48,965,767 (GRCm39) |
N1224I |
probably benign |
Het |
| Myo18a |
A |
G |
11: 77,755,612 (GRCm39) |
Y1983C |
probably damaging |
Het |
| Myo18a |
C |
T |
11: 77,720,699 (GRCm39) |
|
probably benign |
Het |
| Myrfl |
G |
T |
10: 116,664,909 (GRCm39) |
Q374K |
probably damaging |
Het |
| Ndrg1 |
T |
A |
15: 66,818,346 (GRCm39) |
Q87H |
probably benign |
Het |
| Nol9 |
G |
A |
4: 152,131,030 (GRCm39) |
C351Y |
probably damaging |
Het |
| Nr5a1 |
A |
G |
2: 38,598,141 (GRCm39) |
S219P |
probably benign |
Het |
| Or8b43 |
T |
C |
9: 38,360,489 (GRCm39) |
F107S |
possibly damaging |
Het |
| Or8g28 |
A |
T |
9: 39,169,520 (GRCm39) |
Y149* |
probably null |
Het |
| Pcdhb19 |
A |
G |
18: 37,631,690 (GRCm39) |
D495G |
probably damaging |
Het |
| Pfkm |
A |
G |
15: 98,026,123 (GRCm39) |
M573V |
probably damaging |
Het |
| Plec |
A |
T |
15: 76,065,516 (GRCm39) |
L1586Q |
probably damaging |
Het |
| Prelp |
C |
A |
1: 133,843,005 (GRCm39) |
E47* |
probably null |
Het |
| Rbm33 |
T |
A |
5: 28,615,753 (GRCm39) |
I32N |
probably damaging |
Het |
| Rgs12 |
A |
T |
5: 35,183,227 (GRCm39) |
D310V |
probably damaging |
Het |
| Ripor2 |
A |
C |
13: 24,880,512 (GRCm39) |
H404P |
possibly damaging |
Het |
| Sh3d21 |
T |
C |
4: 126,056,034 (GRCm39) |
E124G |
probably benign |
Het |
| Shroom2 |
C |
T |
X: 151,442,549 (GRCm39) |
S872N |
probably benign |
Het |
| Slc44a5 |
A |
G |
3: 153,956,651 (GRCm39) |
Y301C |
probably damaging |
Het |
| Smap1 |
A |
T |
1: 23,930,995 (GRCm39) |
H66Q |
possibly damaging |
Het |
| Smyd1 |
G |
T |
6: 71,198,007 (GRCm39) |
|
probably benign |
Het |
| Sptbn4 |
T |
A |
7: 27,093,573 (GRCm39) |
|
probably benign |
Het |
| Srsf3-ps |
T |
A |
11: 98,516,146 (GRCm39) |
R76* |
probably null |
Het |
| Stag3 |
A |
G |
5: 138,280,955 (GRCm39) |
K49R |
probably damaging |
Het |
| Stim1 |
C |
A |
7: 101,917,758 (GRCm39) |
A46E |
unknown |
Het |
| Stxbp2 |
A |
T |
8: 3,691,971 (GRCm39) |
I538F |
probably benign |
Het |
| Tbc1d19 |
A |
G |
5: 53,992,559 (GRCm39) |
T114A |
probably benign |
Het |
| Tln2 |
G |
A |
9: 67,128,807 (GRCm39) |
|
probably benign |
Het |
| Trmt10a |
T |
A |
3: 137,857,945 (GRCm39) |
|
probably null |
Het |
| Vwde |
G |
A |
6: 13,187,136 (GRCm39) |
H784Y |
probably damaging |
Het |
| Zfp773 |
T |
C |
7: 7,137,232 (GRCm39) |
T121A |
probably benign |
Het |
|
| Other mutations in Gtf2i |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00155:Gtf2i
|
APN |
5 |
134,271,602 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01565:Gtf2i
|
APN |
5 |
134,284,767 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL01743:Gtf2i
|
APN |
5 |
134,315,747 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01809:Gtf2i
|
APN |
5 |
134,278,804 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02553:Gtf2i
|
APN |
5 |
134,274,015 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02814:Gtf2i
|
APN |
5 |
134,315,558 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03018:Gtf2i
|
APN |
5 |
134,318,189 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
IGL03051:Gtf2i
|
APN |
5 |
134,271,768 (GRCm39) |
nonsense |
probably null |
|
|
P0041:Gtf2i
|
UTSW |
5 |
134,273,742 (GRCm39) |
splice site |
probably benign |
|
|
R0330:Gtf2i
|
UTSW |
5 |
134,280,740 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R0515:Gtf2i
|
UTSW |
5 |
134,271,773 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0529:Gtf2i
|
UTSW |
5 |
134,290,723 (GRCm39) |
nonsense |
probably null |
|
|
R0594:Gtf2i
|
UTSW |
5 |
134,271,027 (GRCm39) |
splice site |
probably benign |
|
|
R0650:Gtf2i
|
UTSW |
5 |
134,290,691 (GRCm39) |
splice site |
probably benign |
|
|
R1055:Gtf2i
|
UTSW |
5 |
134,292,478 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1079:Gtf2i
|
UTSW |
5 |
134,271,748 (GRCm39) |
splice site |
probably benign |
|
|
R1916:Gtf2i
|
UTSW |
5 |
134,275,702 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2969:Gtf2i
|
UTSW |
5 |
134,280,746 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3013:Gtf2i
|
UTSW |
5 |
134,324,358 (GRCm39) |
splice site |
probably benign |
|
|
R4392:Gtf2i
|
UTSW |
5 |
134,289,483 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4421:Gtf2i
|
UTSW |
5 |
134,283,891 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R4635:Gtf2i
|
UTSW |
5 |
134,274,028 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4763:Gtf2i
|
UTSW |
5 |
134,284,818 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4770:Gtf2i
|
UTSW |
5 |
134,272,414 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R5063:Gtf2i
|
UTSW |
5 |
134,289,425 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5195:Gtf2i
|
UTSW |
5 |
134,273,686 (GRCm39) |
nonsense |
probably null |
|
|
R5829:Gtf2i
|
UTSW |
5 |
134,292,547 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6005:Gtf2i
|
UTSW |
5 |
134,284,812 (GRCm39) |
nonsense |
probably null |
|
|
R6119:Gtf2i
|
UTSW |
5 |
134,315,911 (GRCm39) |
splice site |
probably null |
|
|
R6576:Gtf2i
|
UTSW |
5 |
134,292,556 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6936:Gtf2i
|
UTSW |
5 |
134,271,639 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7070:Gtf2i
|
UTSW |
5 |
134,311,657 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7071:Gtf2i
|
UTSW |
5 |
134,292,475 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7142:Gtf2i
|
UTSW |
5 |
134,273,705 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7366:Gtf2i
|
UTSW |
5 |
134,294,603 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7694:Gtf2i
|
UTSW |
5 |
134,311,659 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7879:Gtf2i
|
UTSW |
5 |
134,295,471 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R8039:Gtf2i
|
UTSW |
5 |
134,284,688 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R8041:Gtf2i
|
UTSW |
5 |
134,322,599 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8154:Gtf2i
|
UTSW |
5 |
134,280,721 (GRCm39) |
missense |
probably benign |
0.07 |
|
R8365:Gtf2i
|
UTSW |
5 |
134,303,434 (GRCm39) |
missense |
probably benign |
0.22 |
|
R8706:Gtf2i
|
UTSW |
5 |
134,278,733 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8738:Gtf2i
|
UTSW |
5 |
134,324,374 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8827:Gtf2i
|
UTSW |
5 |
134,269,096 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8901:Gtf2i
|
UTSW |
5 |
134,324,389 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8902:Gtf2i
|
UTSW |
5 |
134,278,720 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9020:Gtf2i
|
UTSW |
5 |
134,275,415 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9092:Gtf2i
|
UTSW |
5 |
134,318,241 (GRCm39) |
makesense |
probably null |
|
|
R9169:Gtf2i
|
UTSW |
5 |
134,271,534 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9240:Gtf2i
|
UTSW |
5 |
134,292,619 (GRCm39) |
missense |
probably benign |
0.34 |
|
R9333:Gtf2i
|
UTSW |
5 |
134,271,840 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9346:Gtf2i
|
UTSW |
5 |
134,315,781 (GRCm39) |
missense |
probably benign |
|
|
R9346:Gtf2i
|
UTSW |
5 |
134,273,663 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9570:Gtf2i
|
UTSW |
5 |
134,294,627 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9648:Gtf2i
|
UTSW |
5 |
134,284,770 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9702:Gtf2i
|
UTSW |
5 |
134,275,415 (GRCm39) |
missense |
probably benign |
0.03 |
|
X0022:Gtf2i
|
UTSW |
5 |
134,292,470 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Gtf2i
|
UTSW |
5 |
134,292,499 (GRCm39) |
missense |
probably null |
1.00 |
|
| Posted On |
2015-12-18 |
Incidental Mutation