Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap4m1 |
T |
A |
5: 138,173,061 (GRCm39) |
I134N |
probably damaging |
Het |
Cacna1b |
A |
G |
2: 24,542,982 (GRCm39) |
V1294A |
possibly damaging |
Het |
Carmil1 |
A |
T |
13: 24,339,029 (GRCm39) |
S160T |
probably damaging |
Het |
Ccdc7b |
C |
A |
8: 129,857,512 (GRCm39) |
|
probably benign |
Het |
Chd9 |
T |
G |
8: 91,767,812 (GRCm39) |
N2436K |
probably damaging |
Het |
Cradd |
G |
A |
10: 95,158,462 (GRCm39) |
A95V |
probably benign |
Het |
Cttnbp2 |
T |
G |
6: 18,375,952 (GRCm39) |
E1529A |
probably damaging |
Het |
Cyp11b1 |
T |
C |
15: 74,710,387 (GRCm39) |
I305V |
possibly damaging |
Het |
Cyp2j6 |
A |
T |
4: 96,411,983 (GRCm39) |
N428K |
probably damaging |
Het |
Cyp3a44 |
A |
T |
5: 145,731,728 (GRCm39) |
S139R |
probably damaging |
Het |
Dysf |
C |
T |
6: 84,093,105 (GRCm39) |
R1073C |
probably damaging |
Het |
Ei24 |
A |
G |
9: 36,701,498 (GRCm39) |
F23S |
|
Het |
Enam |
T |
C |
5: 88,639,124 (GRCm39) |
|
probably null |
Het |
Ezh2 |
A |
T |
6: 47,531,196 (GRCm39) |
C163S |
probably benign |
Het |
Fam76b |
T |
A |
9: 13,755,381 (GRCm39) |
F329L |
probably benign |
Het |
Gatad2b |
G |
A |
3: 90,263,507 (GRCm39) |
A535T |
probably damaging |
Het |
Gm5622 |
T |
A |
14: 51,796,770 (GRCm39) |
|
probably benign |
Het |
Greb1l |
A |
T |
18: 10,509,257 (GRCm39) |
H523L |
probably benign |
Het |
Grhl3 |
T |
A |
4: 135,288,640 (GRCm39) |
N15I |
probably damaging |
Het |
Gsta3 |
A |
T |
1: 21,330,283 (GRCm39) |
Y95F |
probably benign |
Het |
Htr1f |
C |
A |
16: 64,747,196 (GRCm39) |
G32V |
probably benign |
Het |
Il18r1 |
C |
A |
1: 40,535,016 (GRCm39) |
Q404K |
probably benign |
Het |
Izumo3 |
A |
T |
4: 92,033,216 (GRCm39) |
|
probably null |
Het |
Kctd19 |
T |
A |
8: 106,112,028 (GRCm39) |
I806F |
probably damaging |
Het |
Lama4 |
G |
T |
10: 38,902,587 (GRCm39) |
C187F |
probably damaging |
Het |
Lamp3 |
T |
G |
16: 19,519,788 (GRCm39) |
I132L |
probably benign |
Het |
Ly9 |
A |
T |
1: 171,432,559 (GRCm39) |
Y151* |
probably null |
Het |
Lztr1 |
T |
C |
16: 17,343,402 (GRCm39) |
L474P |
probably benign |
Het |
Mcm9 |
A |
T |
10: 53,502,130 (GRCm39) |
Y79N |
|
Het |
Mocs2 |
T |
A |
13: 114,961,760 (GRCm39) |
N80K |
possibly damaging |
Het |
Mrgbp |
T |
A |
2: 180,224,712 (GRCm39) |
C38S |
probably benign |
Het |
Ncs1 |
G |
T |
2: 31,136,159 (GRCm39) |
|
probably benign |
Het |
Or51a10 |
G |
A |
7: 103,699,055 (GRCm39) |
P169S |
probably benign |
Het |
Or8k17 |
T |
C |
2: 86,066,888 (GRCm39) |
N90S |
probably benign |
Het |
Pakap |
A |
G |
4: 57,709,916 (GRCm39) |
D287G |
probably benign |
Het |
Pax5 |
A |
T |
4: 44,645,621 (GRCm39) |
V236E |
probably benign |
Het |
Pcdhgb5 |
A |
G |
18: 37,865,260 (GRCm39) |
I352V |
probably benign |
Het |
Pik3r5 |
A |
G |
11: 68,385,104 (GRCm39) |
T670A |
probably benign |
Het |
Plxna2 |
T |
A |
1: 194,479,243 (GRCm39) |
N1301K |
possibly damaging |
Het |
Pou2af3 |
A |
G |
9: 51,182,104 (GRCm39) |
L156P |
probably damaging |
Het |
Pou5f2 |
G |
A |
13: 78,173,886 (GRCm39) |
G276D |
probably damaging |
Het |
Ppl |
C |
G |
16: 4,906,854 (GRCm39) |
R1147P |
probably damaging |
Het |
Pramel17 |
T |
C |
4: 101,693,022 (GRCm39) |
K326R |
probably benign |
Het |
Prkdc |
C |
A |
16: 15,545,523 (GRCm39) |
R1880S |
probably damaging |
Het |
Rbfox1 |
T |
A |
16: 7,227,605 (GRCm39) |
D373E |
probably benign |
Het |
Rbm24 |
A |
G |
13: 46,582,780 (GRCm39) |
D233G |
probably damaging |
Het |
Rbp3 |
A |
T |
14: 33,680,588 (GRCm39) |
E1063D |
possibly damaging |
Het |
Rc3h2 |
A |
G |
2: 37,267,941 (GRCm39) |
V939A |
possibly damaging |
Het |
Relb |
C |
A |
7: 19,345,799 (GRCm39) |
V385L |
possibly damaging |
Het |
Robo4 |
T |
G |
9: 37,317,130 (GRCm39) |
S482A |
unknown |
Het |
Ryr1 |
A |
C |
7: 28,774,091 (GRCm39) |
L2426R |
probably damaging |
Het |
Sass6 |
A |
T |
3: 116,407,598 (GRCm39) |
E238V |
possibly damaging |
Het |
Ski |
T |
C |
4: 155,245,047 (GRCm39) |
I400V |
probably benign |
Het |
Slc27a2 |
C |
A |
2: 126,416,656 (GRCm39) |
A336D |
|
Het |
Slc30a3 |
T |
C |
5: 31,250,668 (GRCm39) |
T12A |
possibly damaging |
Het |
Slc6a6 |
T |
C |
6: 91,725,444 (GRCm39) |
V447A |
probably damaging |
Het |
Smad1 |
T |
A |
8: 80,098,554 (GRCm39) |
I87F |
probably damaging |
Het |
Spns1 |
G |
A |
7: 125,971,593 (GRCm39) |
S319F |
possibly damaging |
Het |
Sytl3 |
C |
A |
17: 6,973,410 (GRCm39) |
T237N |
possibly damaging |
Het |
Tdrd7 |
A |
G |
4: 45,987,570 (GRCm39) |
T68A |
probably damaging |
Het |
Tex56 |
T |
A |
13: 35,116,526 (GRCm39) |
W92R |
probably damaging |
Het |
Tmem135 |
G |
C |
7: 88,797,186 (GRCm39) |
L357V |
probably benign |
Het |
Tmem238 |
A |
G |
7: 4,792,520 (GRCm39) |
C8R |
possibly damaging |
Het |
Ubxn2b |
A |
T |
4: 6,216,061 (GRCm39) |
Q328L |
probably damaging |
Het |
Vmn1r226 |
A |
G |
17: 20,908,133 (GRCm39) |
T122A |
probably benign |
Het |
Vps13d |
A |
G |
4: 144,882,648 (GRCm39) |
F982L |
|
Het |
Xpo4 |
T |
C |
14: 57,902,367 (GRCm39) |
E16G |
probably benign |
Het |
Zbtb17 |
T |
A |
4: 141,189,233 (GRCm39) |
M51K |
possibly damaging |
Het |
Zdhhc1 |
A |
G |
8: 106,200,173 (GRCm39) |
F315S |
probably benign |
Het |
Zfp568 |
C |
T |
7: 29,722,459 (GRCm39) |
T468M |
probably damaging |
Het |
|
Other mutations in Gm9195 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R6448:Gm9195
|
UTSW |
14 |
72,671,451 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6617:Gm9195
|
UTSW |
14 |
72,669,215 (GRCm39) |
missense |
probably damaging |
0.99 |
R6833:Gm9195
|
UTSW |
14 |
72,671,856 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6843:Gm9195
|
UTSW |
14 |
72,678,651 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6994:Gm9195
|
UTSW |
14 |
72,718,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R7082:Gm9195
|
UTSW |
14 |
72,680,152 (GRCm39) |
missense |
probably benign |
0.41 |
R7157:Gm9195
|
UTSW |
14 |
72,718,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R7204:Gm9195
|
UTSW |
14 |
72,711,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R7208:Gm9195
|
UTSW |
14 |
72,689,192 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7319:Gm9195
|
UTSW |
14 |
72,697,929 (GRCm39) |
missense |
probably benign |
0.03 |
R7368:Gm9195
|
UTSW |
14 |
72,717,496 (GRCm39) |
missense |
probably damaging |
0.96 |
R7424:Gm9195
|
UTSW |
14 |
72,673,217 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7481:Gm9195
|
UTSW |
14 |
72,720,116 (GRCm39) |
missense |
probably benign |
0.07 |
R7527:Gm9195
|
UTSW |
14 |
72,711,310 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7573:Gm9195
|
UTSW |
14 |
72,694,122 (GRCm39) |
missense |
probably null |
|
R7618:Gm9195
|
UTSW |
14 |
72,690,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R7700:Gm9195
|
UTSW |
14 |
72,693,342 (GRCm39) |
splice site |
probably null |
|
R7740:Gm9195
|
UTSW |
14 |
72,678,113 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7896:Gm9195
|
UTSW |
14 |
72,693,178 (GRCm39) |
missense |
unknown |
|
R8005:Gm9195
|
UTSW |
14 |
72,663,840 (GRCm39) |
missense |
probably benign |
0.07 |
R8124:Gm9195
|
UTSW |
14 |
72,680,063 (GRCm39) |
missense |
probably benign |
0.41 |
R8177:Gm9195
|
UTSW |
14 |
72,697,977 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8353:Gm9195
|
UTSW |
14 |
72,678,201 (GRCm39) |
missense |
probably benign |
0.41 |
R8371:Gm9195
|
UTSW |
14 |
72,697,899 (GRCm39) |
missense |
probably benign |
0.07 |
R8453:Gm9195
|
UTSW |
14 |
72,678,201 (GRCm39) |
missense |
probably benign |
0.41 |
R8700:Gm9195
|
UTSW |
14 |
72,720,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R8821:Gm9195
|
UTSW |
14 |
72,717,536 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8880:Gm9195
|
UTSW |
14 |
72,691,320 (GRCm39) |
missense |
unknown |
|
R8977:Gm9195
|
UTSW |
14 |
72,691,338 (GRCm39) |
missense |
unknown |
|
R9111:Gm9195
|
UTSW |
14 |
72,694,123 (GRCm39) |
nonsense |
probably null |
|
R9157:Gm9195
|
UTSW |
14 |
72,692,038 (GRCm39) |
missense |
unknown |
|
R9172:Gm9195
|
UTSW |
14 |
72,711,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R9234:Gm9195
|
UTSW |
14 |
72,695,786 (GRCm39) |
nonsense |
probably null |
|
R9246:Gm9195
|
UTSW |
14 |
72,710,314 (GRCm39) |
missense |
probably benign |
0.29 |
R9267:Gm9195
|
UTSW |
14 |
72,700,546 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9341:Gm9195
|
UTSW |
14 |
72,717,500 (GRCm39) |
missense |
probably damaging |
0.96 |
R9343:Gm9195
|
UTSW |
14 |
72,717,500 (GRCm39) |
missense |
probably damaging |
0.96 |
R9446:Gm9195
|
UTSW |
14 |
72,717,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R9546:Gm9195
|
UTSW |
14 |
72,718,347 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9676:Gm9195
|
UTSW |
14 |
72,709,667 (GRCm39) |
missense |
unknown |
|
R9739:Gm9195
|
UTSW |
14 |
72,690,264 (GRCm39) |
missense |
probably damaging |
0.96 |
R9764:Gm9195
|
UTSW |
14 |
72,699,885 (GRCm39) |
missense |
unknown |
|
R9797:Gm9195
|
UTSW |
14 |
72,687,705 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Gm9195
|
UTSW |
14 |
72,690,874 (GRCm39) |
frame shift |
probably null |
|
Z1177:Gm9195
|
UTSW |
14 |
72,680,442 (GRCm39) |
missense |
possibly damaging |
0.90 |
|