Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503L19Rik |
T |
C |
18: 70,591,455 (GRCm39) |
N457S |
probably damaging |
Het |
Asic4 |
G |
A |
1: 75,427,567 (GRCm39) |
G31E |
probably benign |
Het |
Atp2a3 |
A |
G |
11: 72,866,223 (GRCm39) |
D281G |
probably damaging |
Het |
Azin1 |
T |
C |
15: 38,491,795 (GRCm39) |
D387G |
probably benign |
Het |
Bdp1 |
T |
C |
13: 100,204,043 (GRCm39) |
M660V |
probably benign |
Het |
Catsperg2 |
G |
A |
7: 29,416,491 (GRCm39) |
T307M |
probably damaging |
Het |
Cfap54 |
T |
G |
10: 92,651,764 (GRCm39) |
K3095N |
probably benign |
Het |
Chl1 |
A |
G |
6: 103,677,504 (GRCm39) |
N706S |
probably damaging |
Het |
Crym |
A |
G |
7: 119,798,517 (GRCm39) |
V113A |
probably benign |
Het |
Cux1 |
A |
G |
5: 136,341,548 (GRCm39) |
S607P |
probably damaging |
Het |
Cyp3a44 |
T |
C |
5: 145,731,207 (GRCm39) |
N198D |
possibly damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Elac1 |
A |
G |
18: 73,875,740 (GRCm39) |
V97A |
probably benign |
Het |
Erbb3 |
G |
A |
10: 128,405,505 (GRCm39) |
T1251M |
probably damaging |
Het |
Gask1b |
T |
A |
3: 79,843,910 (GRCm39) |
N12K |
probably damaging |
Het |
Gprc5c |
G |
T |
11: 114,755,093 (GRCm39) |
V257L |
possibly damaging |
Het |
Hydin |
A |
G |
8: 111,061,416 (GRCm39) |
H316R |
possibly damaging |
Het |
Ikzf3 |
A |
T |
11: 98,381,406 (GRCm39) |
M58K |
probably benign |
Het |
Lyst |
T |
C |
13: 13,835,555 (GRCm39) |
Y1746H |
probably damaging |
Het |
Map3k11 |
T |
A |
19: 5,750,622 (GRCm39) |
N613K |
probably benign |
Het |
Mfng |
C |
T |
15: 78,648,588 (GRCm39) |
R163H |
probably benign |
Het |
Mrm1 |
A |
T |
11: 84,710,086 (GRCm39) |
L38Q |
possibly damaging |
Het |
Myo7b |
A |
G |
18: 32,131,787 (GRCm39) |
F470L |
probably damaging |
Het |
Ndst2 |
G |
A |
14: 20,774,555 (GRCm39) |
R834W |
probably damaging |
Het |
Opa1 |
T |
A |
16: 29,436,948 (GRCm39) |
I637N |
probably benign |
Het |
Or52h9 |
A |
T |
7: 104,203,026 (GRCm39) |
Q300L |
probably benign |
Het |
Or5d43 |
T |
C |
2: 88,104,565 (GRCm39) |
Y276C |
possibly damaging |
Het |
Padi4 |
A |
G |
4: 140,473,442 (GRCm39) |
V665A |
possibly damaging |
Het |
Pcdh1 |
A |
G |
18: 38,325,252 (GRCm39) |
Y897H |
probably damaging |
Het |
Pkp3 |
A |
G |
7: 140,663,190 (GRCm39) |
D345G |
probably damaging |
Het |
Pla2g4a |
T |
C |
1: 149,740,918 (GRCm39) |
M366V |
possibly damaging |
Het |
Pnkp |
C |
T |
7: 44,511,827 (GRCm39) |
S113L |
probably damaging |
Het |
Pon3 |
T |
C |
6: 5,240,860 (GRCm39) |
D34G |
possibly damaging |
Het |
Ppargc1b |
A |
T |
18: 61,448,876 (GRCm39) |
S133T |
probably damaging |
Het |
Ppp4r3b |
T |
C |
11: 29,123,309 (GRCm39) |
S2P |
possibly damaging |
Het |
Rbm20 |
A |
G |
19: 53,801,818 (GRCm39) |
T109A |
probably damaging |
Het |
Rexo5 |
C |
A |
7: 119,443,660 (GRCm39) |
H690Q |
probably benign |
Het |
Scube2 |
C |
T |
7: 109,408,437 (GRCm39) |
G670D |
probably damaging |
Het |
Sipa1l2 |
T |
C |
8: 126,218,865 (GRCm39) |
I157M |
probably damaging |
Het |
Slbp |
A |
T |
5: 33,801,210 (GRCm39) |
I167N |
probably damaging |
Het |
Sry |
C |
G |
Y: 2,662,975 (GRCm39) |
Q228H |
unknown |
Het |
Stk36 |
T |
C |
1: 74,650,317 (GRCm39) |
V283A |
probably benign |
Het |
Tead1 |
A |
G |
7: 112,358,673 (GRCm39) |
|
probably benign |
Het |
Tecpr2 |
G |
C |
12: 110,881,836 (GRCm39) |
W135S |
probably damaging |
Het |
Ttc39a |
A |
T |
4: 109,279,701 (GRCm39) |
I112F |
probably benign |
Het |
Vmn1r128 |
A |
T |
7: 21,083,328 (GRCm39) |
T11S |
probably benign |
Het |
Vnn1 |
G |
A |
10: 23,779,303 (GRCm39) |
C404Y |
probably damaging |
Het |
Wdr41 |
T |
C |
13: 95,131,759 (GRCm39) |
F57L |
probably damaging |
Het |
Zfp975 |
T |
G |
7: 42,311,654 (GRCm39) |
T320P |
probably damaging |
Het |
Zfp985 |
A |
T |
4: 147,667,289 (GRCm39) |
|
probably null |
Het |
Zfpm2 |
T |
C |
15: 40,962,865 (GRCm39) |
S176P |
probably benign |
Het |
|
Other mutations in Tha1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00497:Tha1
|
APN |
11 |
117,761,831 (GRCm39) |
splice site |
probably benign |
|
IGL01434:Tha1
|
APN |
11 |
117,759,425 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01658:Tha1
|
APN |
11 |
117,762,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Tha1
|
UTSW |
11 |
117,759,401 (GRCm39) |
missense |
probably benign |
0.17 |
R0671:Tha1
|
UTSW |
11 |
117,763,983 (GRCm39) |
splice site |
probably benign |
|
R1958:Tha1
|
UTSW |
11 |
117,760,179 (GRCm39) |
unclassified |
probably benign |
|
R2127:Tha1
|
UTSW |
11 |
117,760,600 (GRCm39) |
missense |
probably damaging |
0.98 |
R3416:Tha1
|
UTSW |
11 |
117,764,026 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4825:Tha1
|
UTSW |
11 |
117,760,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R5145:Tha1
|
UTSW |
11 |
117,760,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Tha1
|
UTSW |
11 |
117,760,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R5339:Tha1
|
UTSW |
11 |
117,761,908 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5858:Tha1
|
UTSW |
11 |
117,764,210 (GRCm39) |
missense |
unknown |
|
R6820:Tha1
|
UTSW |
11 |
117,762,504 (GRCm39) |
missense |
probably benign |
0.00 |
R7399:Tha1
|
UTSW |
11 |
117,760,516 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7706:Tha1
|
UTSW |
11 |
117,760,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R7905:Tha1
|
UTSW |
11 |
117,761,893 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8094:Tha1
|
UTSW |
11 |
117,759,323 (GRCm39) |
missense |
probably benign |
0.00 |
R8322:Tha1
|
UTSW |
11 |
117,759,493 (GRCm39) |
missense |
probably damaging |
0.97 |
R9145:Tha1
|
UTSW |
11 |
117,759,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R9703:Tha1
|
UTSW |
11 |
117,761,863 (GRCm39) |
missense |
probably damaging |
0.96 |
|