Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930553M12Rik |
T |
A |
4: 88,786,486 (GRCm39) |
H44L |
unknown |
Het |
Abcc3 |
T |
C |
11: 94,256,051 (GRCm39) |
K478R |
probably benign |
Het |
Ank2 |
A |
T |
3: 126,736,952 (GRCm39) |
|
probably benign |
Het |
Apod |
A |
G |
16: 31,129,950 (GRCm39) |
V2A |
probably benign |
Het |
Armh4 |
C |
A |
14: 50,011,155 (GRCm39) |
S184I |
probably damaging |
Het |
Aspg |
T |
A |
12: 112,092,824 (GRCm39) |
D530E |
probably damaging |
Het |
Atxn7 |
A |
T |
14: 14,100,878 (GRCm38) |
T855S |
probably benign |
Het |
Blmh |
G |
C |
11: 76,859,451 (GRCm39) |
G351R |
probably damaging |
Het |
Cc2d2a |
C |
T |
5: 43,857,321 (GRCm39) |
R454* |
probably null |
Het |
Cenpp |
T |
C |
13: 49,619,233 (GRCm39) |
E188G |
probably damaging |
Het |
Creg2 |
T |
C |
1: 39,662,376 (GRCm39) |
E252G |
probably benign |
Het |
Dot1l |
A |
G |
10: 80,622,857 (GRCm39) |
Y636C |
probably damaging |
Het |
Dpy30 |
A |
G |
17: 74,614,835 (GRCm39) |
I36T |
probably benign |
Het |
Eed |
A |
G |
7: 89,613,935 (GRCm39) |
|
probably null |
Het |
Fmn1 |
A |
G |
2: 113,195,353 (GRCm39) |
D351G |
unknown |
Het |
Fra10ac1 |
C |
T |
19: 38,212,567 (GRCm39) |
|
probably benign |
Het |
Gdpd4 |
T |
A |
7: 97,623,136 (GRCm39) |
I249N |
probably damaging |
Het |
Glb1l2 |
A |
T |
9: 26,676,423 (GRCm39) |
V600D |
probably null |
Het |
Gm13889 |
A |
T |
2: 93,787,459 (GRCm39) |
|
probably benign |
Het |
Gm17654 |
T |
A |
14: 43,813,327 (GRCm39) |
N188Y |
|
Het |
Gm3327 |
T |
C |
14: 44,363,732 (GRCm39) |
F112S |
|
Het |
H2-Ab1 |
T |
C |
17: 34,482,316 (GRCm39) |
S11P |
probably benign |
Het |
Hcn4 |
T |
C |
9: 58,763,000 (GRCm39) |
S522P |
unknown |
Het |
Hfm1 |
T |
C |
5: 107,043,909 (GRCm39) |
T576A |
probably benign |
Het |
Hoxa1 |
A |
G |
6: 52,135,180 (GRCm39) |
S8P |
probably damaging |
Het |
Hoxd13 |
A |
G |
2: 74,499,369 (GRCm39) |
Y239C |
probably damaging |
Het |
Ifih1 |
T |
A |
2: 62,440,859 (GRCm39) |
I485L |
probably benign |
Het |
Ift52 |
G |
A |
2: 162,871,716 (GRCm39) |
V183M |
probably damaging |
Het |
Ikbkb |
A |
G |
8: 23,161,658 (GRCm39) |
V410A |
possibly damaging |
Het |
Il22ra1 |
G |
A |
4: 135,478,473 (GRCm39) |
V515I |
probably benign |
Het |
Klk1b3 |
A |
T |
7: 43,850,863 (GRCm39) |
I132F |
probably damaging |
Het |
Limk2 |
T |
C |
11: 3,305,448 (GRCm39) |
T206A |
possibly damaging |
Het |
Llph |
A |
T |
10: 120,067,240 (GRCm39) |
|
probably benign |
Het |
Lrrc26 |
T |
A |
2: 25,180,087 (GRCm39) |
D29E |
probably benign |
Het |
Ltbp4 |
A |
G |
7: 27,007,191 (GRCm39) |
|
probably null |
Het |
Mageb3 |
A |
T |
2: 121,784,973 (GRCm39) |
V243E |
probably damaging |
Het |
Mfhas1 |
T |
C |
8: 36,055,792 (GRCm39) |
V89A |
probably benign |
Het |
Mycbp2 |
G |
A |
14: 103,393,534 (GRCm39) |
T2899I |
possibly damaging |
Het |
Nckap5 |
A |
T |
1: 126,186,449 (GRCm39) |
|
probably null |
Het |
Ncor1 |
T |
C |
11: 62,275,619 (GRCm39) |
D530G |
probably null |
Het |
Or10ag55-ps1 |
T |
A |
2: 87,114,775 (GRCm39) |
M47K |
probably benign |
Het |
Or56a3b |
C |
T |
7: 104,771,170 (GRCm39) |
R169* |
probably null |
Het |
Pax4 |
A |
G |
6: 28,446,322 (GRCm39) |
I57T |
probably damaging |
Het |
Peg12 |
T |
C |
7: 62,113,711 (GRCm39) |
I129V |
possibly damaging |
Het |
Pex6 |
G |
A |
17: 47,031,447 (GRCm39) |
A416T |
probably benign |
Het |
Pgghg |
G |
A |
7: 140,524,631 (GRCm39) |
R326H |
probably benign |
Het |
Pgk2 |
T |
A |
17: 40,519,366 (GRCm39) |
M21L |
probably benign |
Het |
Polh |
A |
T |
17: 46,509,642 (GRCm39) |
W64R |
probably benign |
Het |
Rassf7 |
T |
A |
7: 140,797,556 (GRCm39) |
H256Q |
probably benign |
Het |
Rc3h2 |
A |
G |
2: 37,265,258 (GRCm39) |
M1184T |
probably benign |
Het |
Ror1 |
A |
T |
4: 100,299,436 (GRCm39) |
E936D |
probably benign |
Het |
Skic3 |
G |
A |
13: 76,283,079 (GRCm39) |
A769T |
probably damaging |
Het |
Slco1b2 |
A |
T |
6: 141,617,974 (GRCm39) |
T440S |
probably damaging |
Het |
Specc1 |
T |
A |
11: 62,008,604 (GRCm39) |
V40E |
probably damaging |
Het |
Tarbp1 |
T |
A |
8: 127,201,234 (GRCm39) |
S191C |
possibly damaging |
Het |
Timm22 |
A |
G |
11: 76,298,071 (GRCm39) |
E14G |
possibly damaging |
Het |
Tpp2 |
T |
A |
1: 44,022,318 (GRCm39) |
D905E |
probably damaging |
Het |
Trav7-5 |
T |
C |
14: 53,768,756 (GRCm39) |
L108P |
probably damaging |
Het |
Ttc9b |
A |
G |
7: 27,353,667 (GRCm39) |
T106A |
probably benign |
Het |
Ttn |
T |
C |
2: 76,545,012 (GRCm39) |
S32697G |
probably damaging |
Het |
Usp17la |
T |
G |
7: 104,510,514 (GRCm39) |
L373R |
probably benign |
Het |
Vmn1r113 |
A |
G |
7: 20,521,427 (GRCm39) |
N73S |
probably benign |
Het |
Vmn1r42 |
T |
C |
6: 89,822,051 (GRCm39) |
T173A |
possibly damaging |
Het |
Vmn2r106 |
A |
G |
17: 20,499,182 (GRCm39) |
V243A |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r25 |
T |
A |
6: 123,800,569 (GRCm39) |
D591V |
probably damaging |
Het |
Zc3h13 |
T |
C |
14: 75,559,227 (GRCm39) |
S379P |
probably benign |
Het |
Zfp870 |
T |
C |
17: 33,102,456 (GRCm39) |
Y292C |
probably damaging |
Het |
Zfp977 |
A |
T |
7: 42,229,786 (GRCm39) |
N246K |
possibly damaging |
Het |
Zp1 |
G |
A |
19: 10,896,104 (GRCm39) |
T207M |
probably damaging |
Het |
|
Other mutations in Cimip3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0675:Cimip3
|
UTSW |
17 |
47,724,701 (GRCm39) |
missense |
probably benign |
0.25 |
R1529:Cimip3
|
UTSW |
17 |
47,724,815 (GRCm39) |
missense |
probably benign |
0.11 |
R2256:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R2257:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R2512:Cimip3
|
UTSW |
17 |
47,724,651 (GRCm39) |
missense |
probably benign |
|
R2883:Cimip3
|
UTSW |
17 |
47,747,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R3498:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3499:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3834:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3835:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3901:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3910:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3911:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R3913:Cimip3
|
UTSW |
17 |
47,744,348 (GRCm39) |
unclassified |
probably benign |
|
R4191:Cimip3
|
UTSW |
17 |
47,747,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R4280:Cimip3
|
UTSW |
17 |
47,724,780 (GRCm39) |
missense |
probably benign |
0.02 |
R8008:Cimip3
|
UTSW |
17 |
47,747,661 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1176:Cimip3
|
UTSW |
17 |
47,724,659 (GRCm39) |
missense |
probably benign |
0.44 |
|