Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
G |
T |
11: 109,833,094 (GRCm39) |
A1202E |
probably damaging |
Het |
Abcc12 |
A |
T |
8: 87,287,101 (GRCm39) |
I155N |
possibly damaging |
Het |
Atf4 |
T |
A |
15: 80,140,640 (GRCm39) |
H47Q |
probably damaging |
Het |
Atm |
T |
A |
9: 53,401,492 (GRCm39) |
D1459V |
possibly damaging |
Het |
Bicral |
A |
G |
17: 47,112,522 (GRCm39) |
S893P |
probably benign |
Het |
Camk2a |
G |
A |
18: 61,097,036 (GRCm39) |
|
probably null |
Het |
Cebpz |
G |
A |
17: 79,244,308 (GRCm39) |
T51I |
probably damaging |
Het |
Cers5 |
A |
T |
15: 99,638,837 (GRCm39) |
D208E |
probably damaging |
Het |
Cimip2b |
T |
C |
4: 43,427,355 (GRCm39) |
|
probably benign |
Het |
Cyp1a2 |
T |
C |
9: 57,586,345 (GRCm39) |
D391G |
possibly damaging |
Het |
Dct |
G |
T |
14: 118,280,682 (GRCm39) |
F111L |
probably benign |
Het |
Ddb1 |
T |
G |
19: 10,599,080 (GRCm39) |
I529S |
probably benign |
Het |
Dhx9 |
G |
T |
1: 153,348,037 (GRCm39) |
Q361K |
probably damaging |
Het |
Dnai3 |
A |
G |
3: 145,768,086 (GRCm39) |
S592P |
probably benign |
Het |
Erbin |
G |
T |
13: 104,022,795 (GRCm39) |
R15S |
probably damaging |
Het |
F13b |
T |
C |
1: 139,434,671 (GRCm39) |
S146P |
possibly damaging |
Het |
Ggnbp2 |
A |
T |
11: 84,727,277 (GRCm39) |
C520S |
probably damaging |
Het |
Gpx3 |
A |
G |
11: 54,800,329 (GRCm39) |
I208V |
probably benign |
Het |
Grk3 |
A |
G |
5: 113,076,629 (GRCm39) |
|
probably benign |
Het |
Heg1 |
T |
G |
16: 33,552,077 (GRCm39) |
I762R |
probably damaging |
Het |
Ints11 |
A |
T |
4: 155,971,343 (GRCm39) |
T264S |
probably damaging |
Het |
Ints14 |
T |
C |
9: 64,887,113 (GRCm39) |
L348P |
probably damaging |
Het |
Maco1 |
C |
A |
4: 134,555,528 (GRCm39) |
C315F |
probably benign |
Het |
Marf1 |
C |
A |
16: 13,959,919 (GRCm39) |
|
probably benign |
Het |
Med13 |
A |
G |
11: 86,174,075 (GRCm39) |
Y1808H |
probably damaging |
Het |
Mef2a |
G |
T |
7: 66,884,896 (GRCm39) |
S406* |
probably null |
Het |
Mrpl45 |
A |
T |
11: 97,214,714 (GRCm39) |
T134S |
probably benign |
Het |
Myh8 |
A |
G |
11: 67,189,453 (GRCm39) |
I1210V |
probably benign |
Het |
Nsd3 |
T |
C |
8: 26,131,303 (GRCm39) |
S223P |
probably damaging |
Het |
Or2j6 |
T |
G |
7: 139,980,813 (GRCm39) |
S49R |
possibly damaging |
Het |
Or4c115 |
A |
G |
2: 88,927,606 (GRCm39) |
F222L |
probably benign |
Het |
Or5be3 |
A |
T |
2: 86,864,459 (GRCm39) |
Y35* |
probably null |
Het |
P3h3 |
T |
A |
6: 124,818,644 (GRCm39) |
E731D |
probably damaging |
Het |
Pcdhac2 |
A |
G |
18: 37,279,527 (GRCm39) |
R836G |
probably benign |
Het |
Pdzd2 |
A |
G |
15: 12,376,385 (GRCm39) |
V1250A |
probably benign |
Het |
Pgbd1 |
G |
A |
13: 21,618,600 (GRCm39) |
T19I |
possibly damaging |
Het |
Phtf2 |
T |
A |
5: 21,018,249 (GRCm39) |
R31* |
probably null |
Het |
Plod2 |
T |
A |
9: 92,475,799 (GRCm39) |
V294D |
probably benign |
Het |
Rassf5 |
C |
T |
1: 131,172,720 (GRCm39) |
G50R |
probably damaging |
Het |
Rexo5 |
A |
G |
7: 119,444,606 (GRCm39) |
T694A |
probably benign |
Het |
Rtcb |
A |
C |
10: 85,787,315 (GRCm39) |
S82A |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,172,042 (GRCm39) |
L255P |
probably damaging |
Het |
Slc35c1 |
A |
G |
2: 92,284,859 (GRCm39) |
F252L |
probably damaging |
Het |
Slco6d1 |
A |
T |
1: 98,427,472 (GRCm39) |
|
probably benign |
Het |
Sox10 |
T |
G |
15: 79,047,485 (GRCm39) |
|
probably benign |
Het |
Stard9 |
A |
G |
2: 120,529,028 (GRCm39) |
M1762V |
probably benign |
Het |
Stat3 |
A |
T |
11: 100,798,909 (GRCm39) |
Y94N |
probably damaging |
Het |
Tasor |
T |
C |
14: 27,183,107 (GRCm39) |
I522T |
probably benign |
Het |
Tecta |
T |
A |
9: 42,256,930 (GRCm39) |
Y1582F |
probably benign |
Het |
Tex44 |
A |
G |
1: 86,355,453 (GRCm39) |
D454G |
probably damaging |
Het |
Tle6 |
A |
G |
10: 81,431,253 (GRCm39) |
|
probably benign |
Het |
Tmod2 |
T |
C |
9: 75,484,041 (GRCm39) |
E303G |
probably damaging |
Het |
Trem1 |
A |
G |
17: 48,544,245 (GRCm39) |
D90G |
possibly damaging |
Het |
Trhde |
A |
T |
10: 114,284,229 (GRCm39) |
D751E |
probably benign |
Het |
Ttn |
A |
T |
2: 76,795,589 (GRCm39) |
|
probably null |
Het |
Vars2 |
T |
C |
17: 35,970,068 (GRCm39) |
T774A |
probably benign |
Het |
|
Other mutations in Heatr9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02160:Heatr9
|
APN |
11 |
83,409,651 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02832:Heatr9
|
APN |
11 |
83,409,672 (GRCm39) |
splice site |
probably benign |
|
IGL03325:Heatr9
|
APN |
11 |
83,404,085 (GRCm39) |
splice site |
probably null |
|
R0084:Heatr9
|
UTSW |
11 |
83,403,721 (GRCm39) |
splice site |
probably benign |
|
R0243:Heatr9
|
UTSW |
11 |
83,404,164 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0326:Heatr9
|
UTSW |
11 |
83,405,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R1386:Heatr9
|
UTSW |
11 |
83,409,651 (GRCm39) |
missense |
probably benign |
0.00 |
R1914:Heatr9
|
UTSW |
11 |
83,409,035 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1915:Heatr9
|
UTSW |
11 |
83,409,035 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4078:Heatr9
|
UTSW |
11 |
83,403,254 (GRCm39) |
missense |
probably benign |
0.24 |
R4756:Heatr9
|
UTSW |
11 |
83,407,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R4789:Heatr9
|
UTSW |
11 |
83,410,018 (GRCm39) |
missense |
probably benign |
0.06 |
R4999:Heatr9
|
UTSW |
11 |
83,409,618 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5060:Heatr9
|
UTSW |
11 |
83,403,258 (GRCm39) |
missense |
probably benign |
0.20 |
R5506:Heatr9
|
UTSW |
11 |
83,405,592 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5874:Heatr9
|
UTSW |
11 |
83,405,426 (GRCm39) |
missense |
probably benign |
0.36 |
R5922:Heatr9
|
UTSW |
11 |
83,403,193 (GRCm39) |
critical splice donor site |
probably null |
|
R6322:Heatr9
|
UTSW |
11 |
83,407,538 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7007:Heatr9
|
UTSW |
11 |
83,411,446 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7431:Heatr9
|
UTSW |
11 |
83,410,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R7790:Heatr9
|
UTSW |
11 |
83,409,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Heatr9
|
UTSW |
11 |
83,403,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R8154:Heatr9
|
UTSW |
11 |
83,402,703 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9248:Heatr9
|
UTSW |
11 |
83,409,281 (GRCm39) |
missense |
possibly damaging |
0.80 |
|