Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110008L16Rik |
G |
A |
12: 55,304,415 |
V170M |
possibly damaging |
Het |
5031439G07Rik |
A |
T |
15: 84,953,136 |
H325Q |
probably damaging |
Het |
Aasdh |
T |
C |
5: 76,901,925 |
I75V |
probably benign |
Het |
Abca14 |
G |
A |
7: 120,227,444 |
D438N |
possibly damaging |
Het |
Abca8a |
T |
A |
11: 110,089,967 |
I82F |
probably benign |
Het |
Abca8b |
G |
T |
11: 109,981,717 |
N19K |
probably damaging |
Het |
Acan |
A |
G |
7: 79,108,148 |
N506S |
|
Het |
Alox12e |
C |
A |
11: 70,315,905 |
R652L |
probably benign |
Het |
Atad3a |
A |
G |
4: 155,754,041 |
V173A |
probably benign |
Het |
Atl3 |
A |
G |
19: 7,529,068 |
K326R |
probably null |
Het |
Atm |
G |
T |
9: 53,511,917 |
C636* |
probably null |
Het |
Atp2c2 |
G |
A |
8: 119,745,561 |
M451I |
probably benign |
Het |
B020004J07Rik |
A |
G |
4: 101,837,368 |
F106S |
probably benign |
Het |
Best1 |
A |
T |
19: 9,992,115 |
M193K |
probably benign |
Het |
Bmper |
G |
T |
9: 23,399,355 |
G362C |
probably damaging |
Het |
Brd4 |
T |
A |
17: 32,225,583 |
Y139F |
unknown |
Het |
Bzw2 |
A |
T |
12: 36,123,951 |
I108N |
possibly damaging |
Het |
Cbs |
C |
A |
17: 31,619,217 |
V353L |
probably benign |
Het |
Ceacam20 |
A |
G |
7: 19,967,753 |
T22A |
probably damaging |
Het |
Ckap2l |
C |
T |
2: 129,275,516 |
E580K |
probably damaging |
Het |
Ckmt1 |
T |
C |
2: 121,358,893 |
L15P |
possibly damaging |
Het |
Clec18a |
G |
T |
8: 111,081,572 |
P66H |
probably benign |
Het |
Cma1 |
G |
T |
14: 55,942,663 |
T95K |
probably benign |
Het |
Csmd3 |
A |
G |
15: 48,457,598 |
V272A |
probably damaging |
Het |
Ctnna3 |
A |
T |
10: 64,834,589 |
E632D |
probably benign |
Het |
Ctsc |
T |
C |
7: 88,297,153 |
L130P |
probably damaging |
Het |
Frmpd2 |
A |
T |
14: 33,507,475 |
R339S |
probably damaging |
Het |
Frrs1 |
C |
A |
3: 116,880,776 |
S69* |
probably null |
Het |
Gcc2 |
A |
T |
10: 58,280,594 |
E1108D |
probably benign |
Het |
Gkn1 |
A |
T |
6: 87,349,153 |
|
probably null |
Het |
Gtf2a1 |
A |
T |
12: 91,567,724 |
M252K |
probably benign |
Het |
H2-Ob |
T |
C |
17: 34,241,260 |
F115S |
probably damaging |
Het |
Ighv1-53 |
T |
C |
12: 115,158,515 |
N80S |
probably benign |
Het |
Ighv1-67 |
T |
C |
12: 115,604,046 |
K82R |
probably benign |
Het |
Ints1 |
A |
T |
5: 139,762,073 |
I1193N |
possibly damaging |
Het |
Kmt2c |
A |
G |
5: 25,344,925 |
F1353L |
probably damaging |
Het |
Luc7l |
C |
T |
17: 26,253,245 |
|
probably benign |
Het |
Man1a |
A |
C |
10: 53,920,235 |
S454A |
possibly damaging |
Het |
Mars2 |
C |
A |
1: 55,238,063 |
A275D |
probably damaging |
Het |
Nrde2 |
A |
G |
12: 100,130,919 |
V874A |
probably benign |
Het |
Ociad1 |
A |
G |
5: 73,313,466 |
T244A |
probably benign |
Het |
Olfr139 |
A |
T |
11: 74,044,763 |
D170E |
possibly damaging |
Het |
Olfr25 |
A |
T |
9: 38,329,750 |
L51F |
probably damaging |
Het |
Olfr418 |
A |
G |
1: 173,270,244 |
Y23C |
possibly damaging |
Het |
Ovca2 |
A |
G |
11: 75,178,675 |
C41R |
possibly damaging |
Het |
Pacsin2 |
A |
T |
15: 83,385,059 |
D11E |
probably damaging |
Het |
Pcdh15 |
G |
A |
10: 74,342,609 |
S566N |
possibly damaging |
Het |
Pde3b |
A |
G |
7: 114,536,062 |
I1038M |
probably damaging |
Het |
Pi16 |
C |
A |
17: 29,319,234 |
P7Q |
possibly damaging |
Het |
Pkhd1 |
T |
A |
1: 20,523,126 |
T1588S |
possibly damaging |
Het |
Ppig |
A |
G |
2: 69,749,976 |
D618G |
unknown |
Het |
Prss51 |
A |
T |
14: 64,095,995 |
K18* |
probably null |
Het |
Ptpra |
T |
A |
2: 130,544,497 |
D622E |
probably damaging |
Het |
Ptprs |
A |
T |
17: 56,418,988 |
F1431L |
probably benign |
Het |
Pxdn |
A |
G |
12: 29,994,480 |
I486V |
probably benign |
Het |
Rnpc3 |
G |
A |
3: 113,628,355 |
A77V |
probably benign |
Het |
Rtl10 |
T |
A |
16: 18,501,276 |
C85* |
probably null |
Het |
Skint10 |
A |
G |
4: 112,728,973 |
S149P |
probably benign |
Het |
Slc17a8 |
A |
C |
10: 89,576,413 |
V570G |
probably benign |
Het |
Slc25a42 |
A |
T |
8: 70,189,498 |
V98E |
probably damaging |
Het |
Smco2 |
A |
G |
6: 146,858,865 |
E73G |
probably benign |
Het |
Ss18 |
T |
C |
18: 14,679,420 |
Y38C |
probably damaging |
Het |
Tbccd1 |
A |
G |
16: 22,833,997 |
Y125H |
probably benign |
Het |
Tdrd9 |
A |
G |
12: 112,014,454 |
T446A |
probably damaging |
Het |
Tecta |
G |
T |
9: 42,343,887 |
Q1672K |
probably benign |
Het |
Tek |
G |
C |
4: 94,804,304 |
W216C |
probably damaging |
Het |
Timm17a |
C |
T |
1: 135,313,575 |
|
probably null |
Het |
Tlr4 |
A |
T |
4: 66,839,951 |
H327L |
probably benign |
Het |
Trim33 |
T |
C |
3: 103,326,793 |
I449T |
possibly damaging |
Het |
Vmn1r57 |
A |
G |
7: 5,220,560 |
N28S |
probably null |
Het |
Vmn2r117 |
T |
A |
17: 23,477,203 |
H410L |
probably damaging |
Het |
Vmn2r16 |
A |
G |
5: 109,360,906 |
E500G |
probably damaging |
Het |
Wif1 |
A |
G |
10: 121,090,114 |
N245S |
possibly damaging |
Het |
|