Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca6 |
G |
A |
11: 110,135,042 (GRCm39) |
Q248* |
probably null |
Het |
Adgrf4 |
A |
T |
17: 42,978,283 (GRCm39) |
C353* |
probably null |
Het |
Aifm3 |
T |
C |
16: 17,317,604 (GRCm39) |
V75A |
probably benign |
Het |
Apc |
A |
G |
18: 34,445,311 (GRCm39) |
K736E |
possibly damaging |
Het |
Atad2 |
A |
G |
15: 57,989,973 (GRCm39) |
S168P |
probably damaging |
Het |
Ccdc122 |
T |
A |
14: 77,306,313 (GRCm39) |
V28E |
probably damaging |
Het |
Cd5l |
T |
C |
3: 87,268,201 (GRCm39) |
V16A |
probably benign |
Het |
Cdk11b |
T |
C |
4: 155,733,589 (GRCm39) |
S682P |
unknown |
Het |
Chd8 |
T |
C |
14: 52,453,408 (GRCm39) |
I1218V |
probably damaging |
Het |
Clec1b |
A |
C |
6: 129,382,167 (GRCm39) |
I215L |
probably benign |
Het |
Dnah14 |
A |
C |
1: 181,420,992 (GRCm39) |
|
probably null |
Het |
Ednrb |
T |
C |
14: 104,080,459 (GRCm39) |
I152V |
probably benign |
Het |
Epha8 |
G |
T |
4: 136,665,897 (GRCm39) |
L420M |
probably damaging |
Het |
Epn2 |
T |
C |
11: 61,437,407 (GRCm39) |
E55G |
probably damaging |
Het |
Ern1 |
A |
G |
11: 106,300,853 (GRCm39) |
S514P |
probably benign |
Het |
Fbxo4 |
G |
A |
15: 3,998,493 (GRCm39) |
P322S |
probably damaging |
Het |
Gli3 |
T |
A |
13: 15,788,443 (GRCm39) |
D149E |
probably benign |
Het |
Gm12258 |
A |
G |
11: 58,749,922 (GRCm39) |
K366E |
unknown |
Het |
Grb10 |
A |
G |
11: 11,893,919 (GRCm39) |
I389T |
probably benign |
Het |
Grip1 |
G |
A |
10: 119,874,569 (GRCm39) |
E778K |
possibly damaging |
Het |
Hexb |
T |
C |
13: 97,322,176 (GRCm39) |
D203G |
probably damaging |
Het |
Hhatl |
A |
G |
9: 121,618,649 (GRCm39) |
Y118H |
probably damaging |
Het |
Ighv1-69 |
A |
G |
12: 115,586,885 (GRCm39) |
F83L |
possibly damaging |
Het |
Iglon5 |
A |
T |
7: 43,123,891 (GRCm39) |
M336K |
probably benign |
Het |
Iyd |
A |
T |
10: 3,501,884 (GRCm39) |
I177F |
possibly damaging |
Het |
Kdm4c |
A |
C |
4: 74,323,104 (GRCm39) |
D1012A |
possibly damaging |
Het |
Klhl12 |
T |
A |
1: 134,413,562 (GRCm39) |
L349Q |
probably damaging |
Het |
Lrp2 |
A |
G |
2: 69,287,165 (GRCm39) |
|
probably null |
Het |
Mrm2 |
T |
A |
5: 140,314,334 (GRCm39) |
H167L |
probably damaging |
Het |
Mrpl50 |
T |
A |
4: 49,514,338 (GRCm39) |
H111L |
probably damaging |
Het |
Mtcl3 |
C |
A |
10: 29,022,805 (GRCm39) |
R51S |
probably damaging |
Het |
Nags |
A |
T |
11: 102,039,081 (GRCm39) |
T471S |
probably damaging |
Het |
Nod2 |
A |
T |
8: 89,379,621 (GRCm39) |
R41W |
probably benign |
Het |
Notch1 |
T |
A |
2: 26,371,127 (GRCm39) |
N320Y |
probably damaging |
Het |
Nr2c1 |
A |
G |
10: 94,026,528 (GRCm39) |
K468E |
possibly damaging |
Het |
Nsf |
G |
A |
11: 103,801,275 (GRCm39) |
Q247* |
probably null |
Het |
Obsl1 |
T |
C |
1: 75,482,030 (GRCm39) |
H280R |
probably damaging |
Het |
Or4p20 |
T |
C |
2: 88,254,049 (GRCm39) |
M107V |
probably benign |
Het |
Pcdha3 |
C |
T |
18: 37,079,389 (GRCm39) |
R44C |
probably damaging |
Het |
Pcsk4 |
A |
G |
10: 80,157,741 (GRCm39) |
S623P |
possibly damaging |
Het |
Pdcd6ip |
A |
T |
9: 113,484,174 (GRCm39) |
Y818N |
unknown |
Het |
Plk2 |
T |
A |
13: 110,535,301 (GRCm39) |
I445K |
possibly damaging |
Het |
Pramel51 |
C |
A |
12: 88,148,651 (GRCm39) |
|
probably benign |
Het |
Prdm2 |
A |
T |
4: 142,861,561 (GRCm39) |
S576R |
probably damaging |
Het |
Prl3d1 |
A |
T |
13: 27,278,982 (GRCm39) |
Y59F |
probably benign |
Het |
Ptprj |
C |
T |
2: 90,274,805 (GRCm39) |
V1186I |
probably benign |
Het |
Raly |
AGCAGCAGTGGTGGAGGAGGAGGCAGCAGTGGTGGAGG |
AGCAGCAGTGGTGGAGG |
2: 154,705,754 (GRCm39) |
|
probably benign |
Het |
Ros1 |
C |
T |
10: 51,994,215 (GRCm39) |
|
probably null |
Het |
Ryr2 |
C |
T |
13: 11,602,101 (GRCm39) |
|
probably null |
Het |
Scn7a |
A |
T |
2: 66,582,603 (GRCm39) |
I98N |
possibly damaging |
Het |
Spi1 |
T |
A |
2: 90,943,617 (GRCm39) |
S54T |
probably benign |
Het |
Ssna1 |
C |
T |
2: 25,162,316 (GRCm39) |
V16I |
probably benign |
Het |
Sult3a2 |
G |
A |
10: 33,655,670 (GRCm39) |
P103L |
possibly damaging |
Het |
Syne1 |
C |
T |
10: 5,193,123 (GRCm39) |
G3975D |
probably damaging |
Het |
Tbc1d1 |
T |
C |
5: 64,330,950 (GRCm39) |
V43A |
possibly damaging |
Het |
Tut4 |
A |
G |
4: 108,370,429 (GRCm39) |
D776G |
probably benign |
Het |
Uba5 |
A |
G |
9: 103,931,567 (GRCm39) |
S222P |
probably damaging |
Het |
Vmn2r24 |
A |
C |
6: 123,764,266 (GRCm39) |
E381A |
probably damaging |
Het |
Vmn2r95 |
G |
A |
17: 18,661,721 (GRCm39) |
G489D |
probably benign |
Het |
Wdr17 |
A |
T |
8: 55,112,735 (GRCm39) |
F789I |
probably damaging |
Het |
Xpnpep1 |
A |
T |
19: 52,990,959 (GRCm39) |
L422Q |
probably damaging |
Het |
Zfand3 |
T |
A |
17: 30,372,302 (GRCm39) |
H107Q |
probably benign |
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 |
R8836:Gm9195
|
UTSW |
14 |
72,695,830 (GRCm39) |
missense |
probably benign |
0.07 |
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 |
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 |
|