Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm5 |
A |
G |
4: 144,504,521 (GRCm39) |
L210P |
probably damaging |
Het |
Acacb |
G |
A |
5: 114,356,923 (GRCm39) |
V1285I |
probably damaging |
Het |
Acly |
A |
T |
11: 100,386,789 (GRCm39) |
I591N |
probably damaging |
Het |
Acr |
T |
A |
15: 89,457,427 (GRCm39) |
V225E |
probably damaging |
Het |
Actr8 |
A |
G |
14: 29,714,925 (GRCm39) |
D580G |
probably damaging |
Het |
Adamts12 |
C |
A |
15: 11,345,734 (GRCm39) |
Q1592K |
probably benign |
Het |
Aire |
T |
C |
10: 77,878,404 (GRCm39) |
E138G |
probably damaging |
Het |
Apob |
C |
T |
12: 8,056,884 (GRCm39) |
Q1789* |
probably null |
Het |
Cbx5 |
A |
C |
15: 103,114,256 (GRCm39) |
|
probably null |
Het |
Cd300lb |
A |
T |
11: 114,819,345 (GRCm39) |
W95R |
probably damaging |
Het |
Cdc16 |
A |
G |
8: 13,827,605 (GRCm39) |
T504A |
probably benign |
Het |
Cenpf |
A |
G |
1: 189,389,018 (GRCm39) |
S1605P |
probably damaging |
Het |
Ckap2l |
A |
G |
2: 129,114,455 (GRCm39) |
V596A |
possibly damaging |
Het |
Cntn1 |
T |
C |
15: 92,151,922 (GRCm39) |
W454R |
probably benign |
Het |
Crat |
C |
T |
2: 30,294,577 (GRCm39) |
R497Q |
probably benign |
Het |
Csf2rb |
A |
G |
15: 78,223,099 (GRCm39) |
T104A |
possibly damaging |
Het |
Cyp4a12b |
A |
G |
4: 115,289,760 (GRCm39) |
D209G |
possibly damaging |
Het |
Ddx23 |
T |
C |
15: 98,546,570 (GRCm39) |
E533G |
probably damaging |
Het |
Dscaml1 |
A |
G |
9: 45,660,744 (GRCm39) |
|
probably null |
Het |
Eif3l |
T |
G |
15: 78,968,336 (GRCm39) |
C202G |
probably benign |
Het |
Ephx4 |
T |
G |
5: 107,577,612 (GRCm39) |
M312R |
probably damaging |
Het |
Erich6 |
A |
T |
3: 58,534,112 (GRCm39) |
|
probably null |
Het |
Far2 |
G |
A |
6: 148,075,411 (GRCm39) |
D424N |
probably damaging |
Het |
Fat1 |
C |
A |
8: 45,489,221 (GRCm39) |
N3497K |
probably damaging |
Het |
Fstl3 |
G |
A |
10: 79,615,865 (GRCm39) |
C117Y |
probably damaging |
Het |
Fyb2 |
A |
T |
4: 104,870,499 (GRCm39) |
H700L |
probably benign |
Het |
Gm8356 |
T |
A |
14: 17,691,282 (GRCm39) |
M128L |
probably benign |
Het |
Golim4 |
G |
T |
3: 75,805,442 (GRCm39) |
|
probably null |
Het |
Grm1 |
T |
G |
10: 10,622,403 (GRCm39) |
D440A |
probably benign |
Het |
Gtf2a1 |
A |
G |
12: 91,529,747 (GRCm39) |
V322A |
probably benign |
Het |
Hid1 |
T |
C |
11: 115,243,407 (GRCm39) |
|
probably null |
Het |
Igfals |
G |
A |
17: 25,098,962 (GRCm39) |
V18M |
possibly damaging |
Het |
Klk1b24 |
G |
T |
7: 43,839,688 (GRCm39) |
|
probably null |
Het |
Lmbr1 |
T |
C |
5: 29,551,850 (GRCm39) |
|
probably benign |
Het |
Lrrc40 |
T |
C |
3: 157,746,194 (GRCm39) |
S90P |
probably benign |
Het |
Mapk9 |
T |
C |
11: 49,763,663 (GRCm39) |
Y185H |
probably damaging |
Het |
Marveld2 |
C |
T |
13: 100,748,068 (GRCm39) |
G337D |
probably damaging |
Het |
Mga |
G |
T |
2: 119,776,710 (GRCm39) |
R1539L |
probably damaging |
Het |
Mllt6 |
T |
A |
11: 97,563,442 (GRCm39) |
S342T |
probably benign |
Het |
Ms4a6c |
T |
C |
19: 11,449,893 (GRCm39) |
|
probably null |
Het |
Muc16 |
T |
A |
9: 18,558,064 (GRCm39) |
H2743L |
unknown |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Or10ag60 |
T |
C |
2: 87,438,281 (GRCm39) |
F183S |
probably damaging |
Het |
Plcd3 |
T |
G |
11: 102,962,545 (GRCm39) |
K635N |
probably damaging |
Het |
Prkch |
T |
A |
12: 73,632,301 (GRCm39) |
|
probably null |
Het |
Rb1cc1 |
T |
C |
1: 6,344,441 (GRCm39) |
V1570A |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,415,704 (GRCm39) |
N1803D |
probably benign |
Het |
Rufy3 |
T |
A |
5: 88,746,331 (GRCm39) |
V72E |
probably benign |
Het |
Secisbp2l |
G |
A |
2: 125,613,452 (GRCm39) |
Q181* |
probably null |
Het |
Sgcb |
A |
G |
5: 73,797,188 (GRCm39) |
F191L |
possibly damaging |
Het |
Sgsh |
T |
A |
11: 119,237,183 (GRCm39) |
D477V |
probably damaging |
Het |
Shoc1 |
A |
T |
4: 59,062,286 (GRCm39) |
V924E |
probably damaging |
Het |
Slc22a28 |
C |
A |
19: 8,048,492 (GRCm39) |
S385I |
probably benign |
Het |
Slc26a3 |
T |
C |
12: 31,497,787 (GRCm39) |
V47A |
probably benign |
Het |
Slco2a1 |
A |
T |
9: 102,945,185 (GRCm39) |
I187F |
probably damaging |
Het |
Sltm |
T |
C |
9: 70,481,179 (GRCm39) |
S344P |
unknown |
Het |
Sort1 |
A |
G |
3: 108,246,141 (GRCm39) |
T373A |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,882,274 (GRCm39) |
F474L |
probably benign |
Het |
Tbc1d5 |
G |
T |
17: 51,224,573 (GRCm39) |
A326E |
possibly damaging |
Het |
Tcstv4 |
A |
T |
13: 120,770,017 (GRCm39) |
K112N |
probably damaging |
Het |
Vwa8 |
A |
C |
14: 79,219,674 (GRCm39) |
|
probably null |
Het |
Wdr70 |
G |
A |
15: 7,951,562 (GRCm39) |
T425I |
probably benign |
Het |
Zfp30 |
T |
C |
7: 29,492,231 (GRCm39) |
Y243H |
probably benign |
Het |
Zfp974 |
A |
T |
7: 27,611,559 (GRCm39) |
N55K |
possibly damaging |
Het |
Zftraf1 |
A |
G |
15: 76,530,435 (GRCm39) |
L295P |
probably damaging |
Het |
|
Other mutations in Or2l13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01559:Or2l13
|
APN |
16 |
19,306,209 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01639:Or2l13
|
APN |
16 |
19,305,914 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02105:Or2l13
|
APN |
16 |
19,306,011 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02352:Or2l13
|
APN |
16 |
19,305,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02359:Or2l13
|
APN |
16 |
19,305,927 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03053:Or2l13
|
APN |
16 |
19,305,969 (GRCm39) |
missense |
probably benign |
0.36 |
IGL03168:Or2l13
|
APN |
16 |
19,305,969 (GRCm39) |
missense |
probably benign |
0.36 |
R0576:Or2l13
|
UTSW |
16 |
19,305,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R0920:Or2l13
|
UTSW |
16 |
19,305,680 (GRCm39) |
missense |
probably benign |
0.00 |
R1335:Or2l13
|
UTSW |
16 |
19,305,803 (GRCm39) |
missense |
probably benign |
0.01 |
R1468:Or2l13
|
UTSW |
16 |
19,306,378 (GRCm39) |
missense |
probably benign |
0.15 |
R1468:Or2l13
|
UTSW |
16 |
19,306,378 (GRCm39) |
missense |
probably benign |
0.15 |
R1490:Or2l13
|
UTSW |
16 |
19,305,672 (GRCm39) |
missense |
probably benign |
|
R2095:Or2l13
|
UTSW |
16 |
19,305,681 (GRCm39) |
missense |
probably benign |
|
R3123:Or2l13
|
UTSW |
16 |
19,305,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R4893:Or2l13
|
UTSW |
16 |
19,305,653 (GRCm39) |
missense |
probably benign |
|
R5093:Or2l13
|
UTSW |
16 |
19,306,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5222:Or2l13
|
UTSW |
16 |
19,305,680 (GRCm39) |
missense |
probably benign |
|
R7149:Or2l13
|
UTSW |
16 |
19,306,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R7305:Or2l13
|
UTSW |
16 |
19,306,449 (GRCm39) |
missense |
probably damaging |
0.98 |
R9394:Or2l13
|
UTSW |
16 |
19,306,421 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9640:Or2l13
|
UTSW |
16 |
19,305,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Or2l13
|
UTSW |
16 |
19,306,113 (GRCm39) |
missense |
possibly damaging |
0.95 |
X0020:Or2l13
|
UTSW |
16 |
19,305,840 (GRCm39) |
missense |
probably benign |
0.22 |
Z1088:Or2l13
|
UTSW |
16 |
19,305,798 (GRCm39) |
missense |
possibly damaging |
0.52 |
|