Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510039O18Rik |
T |
A |
4: 148,029,521 (GRCm39) |
V497E |
probably damaging |
Het |
Adcy7 |
T |
G |
8: 89,045,418 (GRCm39) |
|
probably benign |
Het |
Aldh1a2 |
T |
A |
9: 71,193,248 (GRCm39) |
F486I |
possibly damaging |
Het |
Alox12 |
T |
A |
11: 70,145,375 (GRCm39) |
H66L |
probably benign |
Het |
Apoh |
T |
G |
11: 108,288,187 (GRCm39) |
Y102D |
probably damaging |
Het |
Arl9 |
T |
C |
5: 77,154,401 (GRCm39) |
V43A |
possibly damaging |
Het |
Atf6 |
A |
G |
1: 170,616,175 (GRCm39) |
|
probably null |
Het |
Atp4a |
T |
A |
7: 30,412,675 (GRCm39) |
I127N |
possibly damaging |
Het |
AY358078 |
T |
A |
14: 52,043,166 (GRCm39) |
|
probably benign |
Het |
Baat |
T |
G |
4: 49,490,338 (GRCm39) |
K249Q |
probably damaging |
Het |
Brat1 |
C |
T |
5: 140,703,963 (GRCm39) |
Q739* |
probably null |
Het |
C8g |
A |
G |
2: 25,389,089 (GRCm39) |
F165L |
probably damaging |
Het |
Cel |
T |
G |
2: 28,447,967 (GRCm39) |
D353A |
possibly damaging |
Het |
Col6a1 |
G |
T |
10: 76,546,813 (GRCm39) |
T803K |
unknown |
Het |
Cpxm1 |
A |
G |
2: 130,238,277 (GRCm39) |
L95P |
probably benign |
Het |
Ctsr |
A |
G |
13: 61,310,489 (GRCm39) |
|
probably benign |
Het |
Cyth1 |
A |
G |
11: 118,084,439 (GRCm39) |
|
probably null |
Het |
Dync1h1 |
A |
T |
12: 110,583,126 (GRCm39) |
|
probably benign |
Het |
Ezh1 |
C |
T |
11: 101,094,262 (GRCm39) |
C407Y |
probably damaging |
Het |
Fam243 |
T |
C |
16: 92,117,661 (GRCm39) |
Y209C |
probably benign |
Het |
Gm3696 |
A |
T |
14: 18,435,903 (GRCm39) |
W38R |
probably benign |
Het |
Gm9611 |
T |
C |
14: 42,116,622 (GRCm39) |
T39A |
possibly damaging |
Het |
Gnpat |
T |
A |
8: 125,605,372 (GRCm39) |
L287H |
probably damaging |
Het |
Golm1 |
G |
T |
13: 59,792,958 (GRCm39) |
N182K |
possibly damaging |
Het |
Hdac6 |
T |
C |
X: 7,798,013 (GRCm39) |
M899V |
probably benign |
Het |
Hsf3 |
T |
A |
X: 95,358,578 (GRCm39) |
M272L |
probably benign |
Het |
Kif19a |
C |
T |
11: 114,672,625 (GRCm39) |
|
probably benign |
Het |
Lcn2 |
T |
G |
2: 32,276,030 (GRCm39) |
Y100S |
possibly damaging |
Het |
Lrrc8d |
T |
A |
5: 105,960,131 (GRCm39) |
S180R |
probably damaging |
Het |
Ly6h |
A |
G |
15: 75,436,948 (GRCm39) |
|
probably benign |
Het |
Macf1 |
T |
C |
4: 123,403,705 (GRCm39) |
N705D |
probably benign |
Het |
Mst1r |
C |
T |
9: 107,785,043 (GRCm39) |
P234S |
probably benign |
Het |
Myo5a |
T |
A |
9: 75,094,820 (GRCm39) |
|
probably benign |
Het |
Nipa1 |
T |
C |
7: 55,629,409 (GRCm39) |
I235V |
probably benign |
Het |
Nlgn3 |
T |
C |
X: 100,362,228 (GRCm39) |
V399A |
probably benign |
Het |
Or1d2 |
T |
A |
11: 74,255,738 (GRCm39) |
M81K |
possibly damaging |
Het |
Or2b28 |
A |
G |
13: 21,531,377 (GRCm39) |
N93S |
probably benign |
Het |
Pih1d1 |
T |
C |
7: 44,809,399 (GRCm39) |
S289P |
probably benign |
Het |
Ppl |
T |
C |
16: 4,905,508 (GRCm39) |
N1596D |
probably benign |
Het |
Psmb6 |
T |
A |
11: 70,417,412 (GRCm39) |
S114R |
possibly damaging |
Het |
Pum1 |
C |
A |
4: 130,457,854 (GRCm39) |
Q289K |
probably damaging |
Het |
Shkbp1 |
T |
C |
7: 27,054,676 (GRCm39) |
I75V |
probably benign |
Het |
Slc24a3 |
T |
A |
2: 145,444,478 (GRCm39) |
I284N |
probably benign |
Het |
Slc44a3 |
C |
T |
3: 121,320,842 (GRCm39) |
G53D |
probably damaging |
Het |
Slc9a4 |
A |
C |
1: 40,668,565 (GRCm39) |
D736A |
probably benign |
Het |
Stra6 |
A |
G |
9: 58,059,854 (GRCm39) |
D605G |
probably benign |
Het |
Tas2r126 |
T |
A |
6: 42,411,684 (GRCm39) |
H72Q |
probably benign |
Het |
Tbrg1 |
C |
T |
9: 37,564,408 (GRCm39) |
R166Q |
probably benign |
Het |
Thumpd1 |
C |
T |
7: 119,319,925 (GRCm39) |
G14R |
probably benign |
Het |
Ticrr |
C |
T |
7: 79,344,209 (GRCm39) |
T1358I |
probably benign |
Het |
Tmtc2 |
A |
T |
10: 105,184,340 (GRCm39) |
N518K |
probably benign |
Het |
Trpm4 |
C |
A |
7: 44,964,497 (GRCm39) |
W533C |
probably damaging |
Het |
Tsen54 |
T |
C |
11: 115,712,538 (GRCm39) |
Y119H |
possibly damaging |
Het |
Tulp3 |
G |
A |
6: 128,304,597 (GRCm39) |
T219M |
probably damaging |
Het |
Usp19 |
T |
C |
9: 108,376,160 (GRCm39) |
L1000S |
possibly damaging |
Het |
Vps16 |
A |
T |
2: 130,279,616 (GRCm39) |
Y43F |
probably benign |
Het |
Vsig1 |
T |
A |
X: 139,838,429 (GRCm39) |
V283E |
possibly damaging |
Het |
|
Other mutations in Msto1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01307:Msto1
|
APN |
3 |
88,820,993 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01309:Msto1
|
APN |
3 |
88,820,993 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01505:Msto1
|
APN |
3 |
88,818,050 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01914:Msto1
|
APN |
3 |
88,820,210 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02292:Msto1
|
APN |
3 |
88,819,131 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02349:Msto1
|
APN |
3 |
88,818,205 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02510:Msto1
|
APN |
3 |
88,817,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03120:Msto1
|
APN |
3 |
88,818,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Msto1
|
UTSW |
3 |
88,817,542 (GRCm39) |
missense |
probably damaging |
0.97 |
R0110:Msto1
|
UTSW |
3 |
88,818,848 (GRCm39) |
missense |
probably benign |
0.02 |
R0282:Msto1
|
UTSW |
3 |
88,818,884 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0384:Msto1
|
UTSW |
3 |
88,817,646 (GRCm39) |
nonsense |
probably null |
|
R0450:Msto1
|
UTSW |
3 |
88,818,848 (GRCm39) |
missense |
probably benign |
0.02 |
R0469:Msto1
|
UTSW |
3 |
88,818,848 (GRCm39) |
missense |
probably benign |
0.02 |
R0510:Msto1
|
UTSW |
3 |
88,818,848 (GRCm39) |
missense |
probably benign |
0.02 |
R2088:Msto1
|
UTSW |
3 |
88,818,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R2516:Msto1
|
UTSW |
3 |
88,819,200 (GRCm39) |
splice site |
probably null |
|
R4897:Msto1
|
UTSW |
3 |
88,819,559 (GRCm39) |
missense |
probably benign |
0.02 |
R5661:Msto1
|
UTSW |
3 |
88,820,192 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6179:Msto1
|
UTSW |
3 |
88,818,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Msto1
|
UTSW |
3 |
88,819,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R6395:Msto1
|
UTSW |
3 |
88,812,781 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7039:Msto1
|
UTSW |
3 |
88,818,697 (GRCm39) |
missense |
probably damaging |
0.96 |
R7399:Msto1
|
UTSW |
3 |
88,819,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R7557:Msto1
|
UTSW |
3 |
88,817,435 (GRCm39) |
critical splice donor site |
probably null |
|
R7583:Msto1
|
UTSW |
3 |
88,820,236 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7620:Msto1
|
UTSW |
3 |
88,818,614 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7993:Msto1
|
UTSW |
3 |
88,817,481 (GRCm39) |
missense |
probably benign |
0.17 |
R8015:Msto1
|
UTSW |
3 |
88,818,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R8235:Msto1
|
UTSW |
3 |
88,820,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R8693:Msto1
|
UTSW |
3 |
88,819,184 (GRCm39) |
missense |
probably benign |
0.02 |
R9071:Msto1
|
UTSW |
3 |
88,812,414 (GRCm39) |
unclassified |
probably benign |
|
R9246:Msto1
|
UTSW |
3 |
88,819,411 (GRCm39) |
missense |
probably damaging |
0.99 |
|