Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022B05Rik |
A |
T |
8: 125,366,098 (GRCm39) |
I215N |
probably damaging |
Het |
Aig1 |
T |
C |
10: 13,528,757 (GRCm39) |
|
probably null |
Het |
Atp8b2 |
T |
A |
3: 89,861,865 (GRCm39) |
K82N |
possibly damaging |
Het |
Cacnb4 |
T |
G |
2: 52,359,615 (GRCm39) |
Y131S |
probably damaging |
Het |
Cep170b |
G |
A |
12: 112,697,864 (GRCm39) |
S62N |
possibly damaging |
Het |
Crmp1 |
A |
G |
5: 37,422,619 (GRCm39) |
D142G |
probably benign |
Het |
Csf1r |
A |
G |
18: 61,260,957 (GRCm39) |
Q716R |
possibly damaging |
Het |
Cyp2u1 |
T |
C |
3: 131,087,133 (GRCm39) |
T483A |
possibly damaging |
Het |
D930020B18Rik |
T |
C |
10: 121,503,565 (GRCm39) |
F247L |
probably benign |
Het |
Dcaf13 |
T |
C |
15: 39,008,586 (GRCm39) |
L396P |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,353,240 (GRCm39) |
M2798V |
probably benign |
Het |
E030018B13Rik |
A |
T |
7: 63,569,125 (GRCm39) |
T58S |
unknown |
Het |
Eipr1 |
T |
C |
12: 28,897,657 (GRCm39) |
|
probably null |
Het |
Elf1 |
C |
T |
14: 79,817,948 (GRCm39) |
T526M |
possibly damaging |
Het |
Got1 |
A |
G |
19: 43,504,284 (GRCm39) |
S46P |
probably benign |
Het |
Inpp4b |
T |
C |
8: 82,775,160 (GRCm39) |
I786T |
probably benign |
Het |
Kdm1a |
T |
C |
4: 136,279,892 (GRCm39) |
I703M |
probably damaging |
Het |
Krt222 |
A |
T |
11: 99,125,838 (GRCm39) |
S264R |
probably benign |
Het |
Lrrd1 |
A |
C |
5: 3,899,982 (GRCm39) |
S96R |
possibly damaging |
Het |
Ltb |
C |
A |
17: 35,414,906 (GRCm39) |
Y235* |
probably null |
Het |
Mbd2 |
T |
A |
18: 70,751,050 (GRCm39) |
C362S |
probably damaging |
Het |
Mlycd |
T |
A |
8: 120,129,325 (GRCm39) |
I264N |
probably damaging |
Het |
Mri1 |
C |
T |
8: 84,980,933 (GRCm39) |
C199Y |
possibly damaging |
Het |
Muc5ac |
A |
T |
7: 141,349,021 (GRCm39) |
K487* |
probably null |
Het |
Myh13 |
T |
C |
11: 67,249,016 (GRCm39) |
I1274T |
probably damaging |
Het |
Ncdn |
G |
A |
4: 126,642,467 (GRCm39) |
R397W |
probably damaging |
Het |
Ncf1 |
T |
A |
5: 134,258,444 (GRCm39) |
|
probably benign |
Het |
Nipbl |
C |
A |
15: 8,321,032 (GRCm39) |
A2692S |
probably benign |
Het |
Odf2l |
C |
T |
3: 144,854,789 (GRCm39) |
T542I |
possibly damaging |
Het |
Or10a49 |
A |
G |
7: 108,467,698 (GRCm39) |
I221T |
probably damaging |
Het |
Or10al2 |
T |
A |
17: 37,983,145 (GRCm39) |
I77N |
probably damaging |
Het |
Oxsm |
T |
C |
14: 16,242,629 (GRCm38) |
T47A |
possibly damaging |
Het |
Pcdhga3 |
A |
T |
18: 37,807,786 (GRCm39) |
S80C |
probably benign |
Het |
Pcnx2 |
T |
C |
8: 126,512,176 (GRCm39) |
T1377A |
probably benign |
Het |
Phactr3 |
C |
A |
2: 177,924,805 (GRCm39) |
Q252K |
possibly damaging |
Het |
Phf2 |
T |
C |
13: 48,973,101 (GRCm39) |
H385R |
unknown |
Het |
Pkd1l3 |
A |
T |
8: 110,357,937 (GRCm39) |
T820S |
probably benign |
Het |
Plekhg1 |
T |
A |
10: 3,887,966 (GRCm39) |
H353Q |
|
Het |
Prss37 |
T |
A |
6: 40,494,713 (GRCm39) |
E24V |
probably damaging |
Het |
Reln |
A |
G |
5: 22,155,943 (GRCm39) |
F2183S |
probably damaging |
Het |
Slc20a2 |
A |
G |
8: 23,051,407 (GRCm39) |
D480G |
probably damaging |
Het |
Slc8a2 |
C |
T |
7: 15,887,124 (GRCm39) |
T672M |
probably damaging |
Het |
Slf2 |
A |
G |
19: 44,961,666 (GRCm39) |
T1062A |
probably benign |
Het |
Snx29 |
A |
G |
16: 11,223,609 (GRCm39) |
E18G |
possibly damaging |
Het |
Spata31e1 |
C |
T |
13: 49,939,542 (GRCm39) |
V723M |
possibly damaging |
Het |
Srf |
C |
A |
17: 46,860,079 (GRCm39) |
G482V |
possibly damaging |
Het |
Styk1 |
G |
A |
6: 131,287,992 (GRCm39) |
Q124* |
probably null |
Het |
Tcf7l1 |
G |
T |
6: 72,608,226 (GRCm39) |
A385E |
probably damaging |
Het |
Thbs4 |
A |
G |
13: 92,913,495 (GRCm39) |
S142P |
probably benign |
Het |
Tlr1 |
G |
A |
5: 65,083,371 (GRCm39) |
S402F |
probably damaging |
Het |
Tnrc6a |
A |
G |
7: 122,769,635 (GRCm39) |
H475R |
probably benign |
Het |
Trmt10b |
A |
T |
4: 45,314,374 (GRCm39) |
N272I |
probably damaging |
Het |
Ubxn7 |
A |
T |
16: 32,200,471 (GRCm39) |
N409I |
probably benign |
Het |
Vcan |
T |
C |
13: 89,837,930 (GRCm39) |
E2538G |
probably damaging |
Het |
Vmn1r65 |
C |
T |
7: 6,011,387 (GRCm39) |
W282* |
probably null |
Het |
Vmn2r4 |
A |
G |
3: 64,322,497 (GRCm39) |
I74T |
probably benign |
Het |
Wdr97 |
T |
A |
15: 76,241,125 (GRCm39) |
F574I |
|
Het |
Zfp949 |
T |
C |
9: 88,449,340 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Gm8369 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1013:Gm8369
|
UTSW |
19 |
11,489,147 (GRCm39) |
frame shift |
probably null |
|
R4192:Gm8369
|
UTSW |
19 |
11,479,596 (GRCm39) |
missense |
probably damaging |
0.97 |
R5445:Gm8369
|
UTSW |
19 |
11,482,170 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5809:Gm8369
|
UTSW |
19 |
11,482,248 (GRCm39) |
intron |
probably benign |
|
R6258:Gm8369
|
UTSW |
19 |
11,488,973 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6791:Gm8369
|
UTSW |
19 |
11,489,200 (GRCm39) |
unclassified |
probably benign |
|
R9565:Gm8369
|
UTSW |
19 |
11,489,015 (GRCm39) |
missense |
probably benign |
0.00 |
R9683:Gm8369
|
UTSW |
19 |
11,489,097 (GRCm39) |
missense |
probably damaging |
0.97 |
RF004:Gm8369
|
UTSW |
19 |
11,489,118 (GRCm39) |
small insertion |
probably benign |
|
RF006:Gm8369
|
UTSW |
19 |
11,489,128 (GRCm39) |
small insertion |
probably benign |
|
RF008:Gm8369
|
UTSW |
19 |
11,489,118 (GRCm39) |
frame shift |
probably null |
|
RF016:Gm8369
|
UTSW |
19 |
11,489,118 (GRCm39) |
frame shift |
probably null |
|
RF017:Gm8369
|
UTSW |
19 |
11,489,106 (GRCm39) |
frame shift |
probably null |
|
RF018:Gm8369
|
UTSW |
19 |
11,489,106 (GRCm39) |
frame shift |
probably null |
|
RF025:Gm8369
|
UTSW |
19 |
11,489,137 (GRCm39) |
frame shift |
probably null |
|
RF028:Gm8369
|
UTSW |
19 |
11,489,137 (GRCm39) |
nonsense |
probably null |
|
RF032:Gm8369
|
UTSW |
19 |
11,489,142 (GRCm39) |
small insertion |
probably benign |
|
RF033:Gm8369
|
UTSW |
19 |
11,489,142 (GRCm39) |
small insertion |
probably benign |
|
RF035:Gm8369
|
UTSW |
19 |
11,489,137 (GRCm39) |
small insertion |
probably benign |
|
RF036:Gm8369
|
UTSW |
19 |
11,489,142 (GRCm39) |
small insertion |
probably benign |
|
RF037:Gm8369
|
UTSW |
19 |
11,489,146 (GRCm39) |
small insertion |
probably benign |
|
RF039:Gm8369
|
UTSW |
19 |
11,489,146 (GRCm39) |
small insertion |
probably benign |
|
RF039:Gm8369
|
UTSW |
19 |
11,489,122 (GRCm39) |
small insertion |
probably benign |
|
RF041:Gm8369
|
UTSW |
19 |
11,489,122 (GRCm39) |
small insertion |
probably benign |
|
RF042:Gm8369
|
UTSW |
19 |
11,489,142 (GRCm39) |
small insertion |
probably benign |
|
RF042:Gm8369
|
UTSW |
19 |
11,489,137 (GRCm39) |
frame shift |
probably null |
|
RF054:Gm8369
|
UTSW |
19 |
11,489,128 (GRCm39) |
frame shift |
probably null |
|
RF055:Gm8369
|
UTSW |
19 |
11,489,112 (GRCm39) |
frame shift |
probably null |
|
Z1176:Gm8369
|
UTSW |
19 |
11,488,988 (GRCm39) |
missense |
probably damaging |
0.99 |
|