Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
G |
11: 110,188,908 (GRCm39) |
F850L |
probably benign |
Het |
Adam1a |
A |
T |
5: 121,657,411 (GRCm39) |
D627E |
probably damaging |
Het |
Add2 |
C |
A |
6: 86,081,459 (GRCm39) |
|
probably benign |
Het |
Anpep |
T |
C |
7: 79,491,785 (GRCm39) |
N72S |
probably benign |
Het |
Aqp6 |
A |
G |
15: 99,501,655 (GRCm39) |
T238A |
possibly damaging |
Het |
Arhgef38 |
G |
T |
3: 132,912,706 (GRCm39) |
T111K |
|
Het |
Atg10 |
A |
G |
13: 91,189,032 (GRCm39) |
Y93H |
probably damaging |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Cald1 |
A |
G |
6: 34,732,682 (GRCm39) |
N286S |
unknown |
Het |
Caps2 |
A |
T |
10: 112,031,829 (GRCm39) |
I322F |
possibly damaging |
Het |
Cbx3 |
T |
A |
6: 51,455,533 (GRCm39) |
S95T |
probably benign |
Het |
Ccdc24 |
T |
C |
4: 117,727,102 (GRCm39) |
T83A |
unknown |
Het |
Cntn1 |
T |
C |
15: 92,140,864 (GRCm39) |
Y197H |
probably damaging |
Het |
Cpd |
A |
G |
11: 76,675,275 (GRCm39) |
I1282T |
possibly damaging |
Het |
Crat |
A |
T |
2: 30,295,052 (GRCm39) |
S454R |
probably damaging |
Het |
D2hgdh |
G |
A |
1: 93,754,338 (GRCm39) |
V126I |
probably benign |
Het |
Dcst1 |
A |
G |
3: 89,271,558 (GRCm39) |
V75A |
probably benign |
Het |
Dnm1l |
T |
C |
16: 16,176,668 (GRCm39) |
D21G |
probably benign |
Het |
Evc2 |
A |
G |
5: 37,504,823 (GRCm39) |
N74D |
probably benign |
Het |
Gm19965 |
A |
T |
1: 116,748,942 (GRCm39) |
M208L |
|
Het |
Gprc6a |
T |
G |
10: 51,497,182 (GRCm39) |
T454P |
possibly damaging |
Het |
Gprin1 |
C |
T |
13: 54,886,778 (GRCm39) |
V499M |
probably benign |
Het |
Hcn4 |
T |
C |
9: 58,767,880 (GRCm39) |
V1147A |
possibly damaging |
Het |
Ighv1-82 |
A |
C |
12: 115,916,342 (GRCm39) |
V56G |
probably damaging |
Het |
Ins2 |
T |
C |
7: 142,232,505 (GRCm39) |
D93G |
possibly damaging |
Het |
Itgb8 |
A |
G |
12: 119,130,535 (GRCm39) |
S658P |
probably benign |
Het |
Kcnmb1 |
T |
C |
11: 33,920,263 (GRCm39) |
F159L |
probably benign |
Het |
Klf1 |
C |
T |
8: 85,629,954 (GRCm39) |
L260F |
probably benign |
Het |
Larp4 |
T |
A |
15: 99,888,205 (GRCm39) |
S140T |
possibly damaging |
Het |
Maneal |
C |
A |
4: 124,755,542 (GRCm39) |
R140L |
probably benign |
Het |
Mfsd11 |
T |
A |
11: 116,750,323 (GRCm39) |
V114D |
|
Het |
Muc4 |
A |
G |
16: 32,752,617 (GRCm38) |
T832A |
probably benign |
Het |
Myh11 |
T |
G |
16: 14,050,439 (GRCm39) |
I509L |
|
Het |
Myh13 |
A |
T |
11: 67,252,149 (GRCm39) |
E1419V |
probably damaging |
Het |
Myh7b |
A |
G |
2: 155,474,439 (GRCm39) |
E1718G |
probably damaging |
Het |
Myo9b |
T |
A |
8: 71,807,871 (GRCm39) |
|
probably benign |
Het |
Notch1 |
A |
T |
2: 26,367,939 (GRCm39) |
L656Q |
probably benign |
Het |
Nova1 |
A |
G |
12: 46,746,813 (GRCm39) |
I488T |
probably damaging |
Het |
Or51r1 |
A |
T |
7: 102,228,500 (GRCm39) |
E266V |
probably damaging |
Het |
Or5b113 |
A |
T |
19: 13,342,222 (GRCm39) |
T77S |
possibly damaging |
Het |
Or5b21 |
A |
G |
19: 12,839,976 (GRCm39) |
Y279C |
probably damaging |
Het |
Or5d18 |
A |
G |
2: 87,864,697 (GRCm39) |
V262A |
probably damaging |
Het |
Or6c35 |
A |
G |
10: 129,169,623 (GRCm39) |
N291S |
probably damaging |
Het |
Or6d13 |
A |
T |
6: 116,517,990 (GRCm39) |
N192I |
possibly damaging |
Het |
Pax6 |
C |
T |
2: 105,523,097 (GRCm39) |
S325L |
probably benign |
Het |
Phldb1 |
T |
C |
9: 44,619,740 (GRCm39) |
D142G |
probably null |
Het |
Phldb3 |
T |
G |
7: 24,324,048 (GRCm39) |
|
probably benign |
Het |
Pikfyve |
G |
T |
1: 65,235,898 (GRCm39) |
R190L |
probably damaging |
Het |
Plagl2 |
A |
T |
2: 153,074,540 (GRCm39) |
H120Q |
probably damaging |
Het |
Pou2f1 |
A |
T |
1: 165,703,640 (GRCm39) |
|
probably benign |
Het |
Pramel58 |
A |
G |
5: 94,831,836 (GRCm39) |
Y281C |
possibly damaging |
Het |
Prpf6 |
A |
G |
2: 181,250,001 (GRCm39) |
R54G |
possibly damaging |
Het |
Prss33 |
T |
C |
17: 24,052,966 (GRCm39) |
E236G |
probably benign |
Het |
Ptpru |
T |
C |
4: 131,522,278 (GRCm39) |
Y709C |
probably benign |
Het |
Rcc1l |
A |
G |
5: 134,197,057 (GRCm39) |
V212A |
probably benign |
Het |
Rtl1 |
G |
A |
12: 109,560,007 (GRCm39) |
L611F |
|
Het |
Scp2 |
A |
G |
4: 107,931,603 (GRCm39) |
I344T |
possibly damaging |
Het |
Serpinb2 |
A |
T |
1: 107,449,890 (GRCm39) |
D101V |
possibly damaging |
Het |
Slc13a1 |
T |
C |
6: 24,097,662 (GRCm39) |
T422A |
probably damaging |
Het |
Slc38a10 |
G |
T |
11: 120,007,762 (GRCm39) |
T406K |
probably benign |
Het |
Smad4 |
T |
C |
18: 73,782,806 (GRCm39) |
E376G |
probably damaging |
Het |
Smarcb1 |
T |
C |
10: 75,750,916 (GRCm39) |
E115G |
probably benign |
Het |
Spata31h1 |
A |
T |
10: 82,120,928 (GRCm39) |
H4027Q |
probably damaging |
Het |
Taf5 |
G |
A |
19: 47,063,370 (GRCm39) |
V307I |
probably damaging |
Het |
Tnc |
T |
C |
4: 63,938,686 (GRCm39) |
N51S |
possibly damaging |
Het |
Trp53inp2 |
G |
T |
2: 155,228,558 (GRCm39) |
R171L |
possibly damaging |
Het |
Ttc13 |
A |
T |
8: 125,402,021 (GRCm39) |
D579E |
probably benign |
Het |
Ttn |
A |
T |
2: 76,775,896 (GRCm39) |
N1761K |
unknown |
Het |
Ttpa |
C |
T |
4: 20,008,401 (GRCm39) |
|
probably benign |
Het |
Ugt3a1 |
G |
A |
15: 9,362,051 (GRCm39) |
V276I |
probably benign |
Het |
Usp4 |
T |
A |
9: 108,244,011 (GRCm39) |
H296Q |
probably benign |
Het |
Vmn1r119 |
T |
A |
7: 20,745,593 (GRCm39) |
H263L |
possibly damaging |
Het |
Vmn2r81 |
A |
G |
10: 79,103,905 (GRCm39) |
D176G |
|
Het |
Wdr1 |
A |
T |
5: 38,687,468 (GRCm39) |
|
probably benign |
Het |
Zfp488 |
T |
G |
14: 33,692,695 (GRCm39) |
Q156P |
possibly damaging |
Het |
|
Other mutations in Gtf3c5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01817:Gtf3c5
|
APN |
2 |
28,459,301 (GRCm39) |
splice site |
probably null |
|
R0062:Gtf3c5
|
UTSW |
2 |
28,462,198 (GRCm39) |
splice site |
probably benign |
|
R0062:Gtf3c5
|
UTSW |
2 |
28,462,198 (GRCm39) |
splice site |
probably benign |
|
R0395:Gtf3c5
|
UTSW |
2 |
28,467,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R0653:Gtf3c5
|
UTSW |
2 |
28,468,008 (GRCm39) |
missense |
probably benign |
0.34 |
R1232:Gtf3c5
|
UTSW |
2 |
28,461,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R1828:Gtf3c5
|
UTSW |
2 |
28,469,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Gtf3c5
|
UTSW |
2 |
28,457,787 (GRCm39) |
missense |
probably benign |
0.26 |
R3154:Gtf3c5
|
UTSW |
2 |
28,469,548 (GRCm39) |
missense |
probably damaging |
0.96 |
R4247:Gtf3c5
|
UTSW |
2 |
28,461,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Gtf3c5
|
UTSW |
2 |
28,469,596 (GRCm39) |
missense |
probably benign |
0.00 |
R4673:Gtf3c5
|
UTSW |
2 |
28,462,236 (GRCm39) |
missense |
probably benign |
0.20 |
R5092:Gtf3c5
|
UTSW |
2 |
28,472,885 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6009:Gtf3c5
|
UTSW |
2 |
28,461,177 (GRCm39) |
missense |
probably benign |
0.00 |
R6334:Gtf3c5
|
UTSW |
2 |
28,460,474 (GRCm39) |
missense |
probably benign |
0.00 |
R6808:Gtf3c5
|
UTSW |
2 |
28,460,499 (GRCm39) |
missense |
probably damaging |
0.98 |
R7490:Gtf3c5
|
UTSW |
2 |
28,461,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R7544:Gtf3c5
|
UTSW |
2 |
28,469,554 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7940:Gtf3c5
|
UTSW |
2 |
28,458,592 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8003:Gtf3c5
|
UTSW |
2 |
28,459,373 (GRCm39) |
missense |
probably benign |
0.03 |
R8176:Gtf3c5
|
UTSW |
2 |
28,460,429 (GRCm39) |
critical splice donor site |
probably null |
|
R8319:Gtf3c5
|
UTSW |
2 |
28,460,506 (GRCm39) |
missense |
probably benign |
0.00 |
|