Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810009A15Rik |
A |
G |
19: 8,866,587 (GRCm39) |
T47A |
probably damaging |
Het |
Acsm2 |
A |
T |
7: 119,179,939 (GRCm39) |
I386F |
probably benign |
Het |
Actn4 |
A |
T |
7: 28,606,397 (GRCm39) |
D305E |
probably benign |
Het |
Anln |
A |
G |
9: 22,274,136 (GRCm39) |
V567A |
probably damaging |
Het |
Arhgap35 |
A |
G |
7: 16,297,343 (GRCm39) |
I574T |
probably benign |
Het |
Baz1b |
C |
A |
5: 135,233,971 (GRCm39) |
S166Y |
probably damaging |
Het |
Ccdc191 |
T |
C |
16: 43,764,192 (GRCm39) |
L551P |
probably damaging |
Het |
Cdk5rap2 |
T |
C |
4: 70,210,110 (GRCm39) |
T713A |
probably benign |
Het |
Cep290 |
C |
A |
10: 100,330,785 (GRCm39) |
A155E |
possibly damaging |
Het |
Chst8 |
G |
A |
7: 34,447,496 (GRCm39) |
Q41* |
probably null |
Het |
Cyp2j6 |
C |
A |
4: 96,406,344 (GRCm39) |
E476* |
probably null |
Het |
Des |
T |
C |
1: 75,343,434 (GRCm39) |
V439A |
probably benign |
Het |
Dimt1 |
A |
G |
13: 107,093,656 (GRCm39) |
T283A |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 50,024,567 (GRCm39) |
V1747D |
possibly damaging |
Het |
Fhod1 |
G |
A |
8: 106,064,694 (GRCm39) |
R137* |
probably null |
Het |
Gab2 |
A |
T |
7: 96,953,448 (GRCm39) |
D608V |
probably damaging |
Het |
Gdpd1 |
T |
C |
11: 86,950,264 (GRCm39) |
D103G |
possibly damaging |
Het |
Hspa5 |
T |
C |
2: 34,664,610 (GRCm39) |
S355P |
probably benign |
Het |
Ide |
A |
T |
19: 37,265,536 (GRCm39) |
F619L |
|
Het |
Ifrd1 |
A |
C |
12: 40,267,225 (GRCm39) |
D70E |
probably benign |
Het |
Il18r1 |
T |
A |
1: 40,513,884 (GRCm39) |
V30E |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kcng1 |
A |
G |
2: 168,111,152 (GRCm39) |
L4S |
probably damaging |
Het |
Lrfn4 |
A |
G |
19: 4,664,357 (GRCm39) |
F59S |
probably damaging |
Het |
Lrrc15 |
T |
C |
16: 30,092,829 (GRCm39) |
D170G |
probably damaging |
Het |
Mettl21e |
T |
A |
1: 44,245,536 (GRCm39) |
M237L |
probably benign |
Het |
Myh1 |
A |
G |
11: 67,102,049 (GRCm39) |
K810E |
probably benign |
Het |
Nbea |
T |
C |
3: 55,573,011 (GRCm39) |
D2524G |
probably damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Or10g3b |
A |
T |
14: 52,586,678 (GRCm39) |
L275H |
probably damaging |
Het |
Or2a5 |
G |
T |
6: 42,873,835 (GRCm39) |
C150F |
probably benign |
Het |
Or2t49 |
T |
C |
11: 58,392,576 (GRCm39) |
T275A |
possibly damaging |
Het |
Or51q1 |
T |
G |
7: 103,629,198 (GRCm39) |
F266L |
probably damaging |
Het |
Or6k2 |
T |
A |
1: 173,986,552 (GRCm39) |
I71K |
possibly damaging |
Het |
Or7a39 |
A |
G |
10: 78,715,597 (GRCm39) |
H197R |
probably benign |
Het |
Pate4 |
A |
G |
9: 35,519,538 (GRCm39) |
S51P |
probably damaging |
Het |
Rbm19 |
T |
C |
5: 120,265,232 (GRCm39) |
|
probably null |
Het |
Rnf139 |
A |
G |
15: 58,770,664 (GRCm39) |
K230E |
probably damaging |
Het |
Rpia |
G |
A |
6: 70,754,377 (GRCm39) |
Q134* |
probably null |
Het |
Rsf1 |
GC |
GCGGCGGCGCC |
7: 97,229,141 (GRCm39) |
|
probably benign |
Het |
Sbk2 |
G |
A |
7: 4,960,277 (GRCm39) |
P298S |
possibly damaging |
Het |
Scrt1 |
A |
G |
15: 76,403,292 (GRCm39) |
S233P |
unknown |
Het |
Sh2b1 |
CGGGGACCAGCTC |
CGGGGACCAGCTCAGCCAAGGGGACCAGCTC |
7: 126,066,760 (GRCm39) |
|
probably benign |
Het |
Sppl2c |
T |
A |
11: 104,078,153 (GRCm39) |
Y318N |
probably benign |
Het |
St6galnac4 |
G |
A |
2: 32,485,739 (GRCm39) |
W215* |
probably null |
Het |
Stxbp6 |
A |
G |
12: 45,066,360 (GRCm39) |
L15P |
probably benign |
Het |
Tmem104 |
T |
C |
11: 115,091,699 (GRCm39) |
L74P |
probably damaging |
Het |
Tnfrsf10b |
A |
G |
14: 70,015,221 (GRCm39) |
D233G |
probably benign |
Het |
Trmt11 |
A |
C |
10: 30,434,938 (GRCm39) |
Y369* |
probably null |
Het |
Tusc1 |
T |
A |
4: 93,223,245 (GRCm39) |
H138L |
probably benign |
Het |
Ush2a |
T |
A |
1: 188,596,937 (GRCm39) |
Y3892* |
probably null |
Het |
Xirp2 |
A |
T |
2: 67,344,280 (GRCm39) |
I2174F |
possibly damaging |
Het |
Zfp947 |
C |
T |
17: 22,364,582 (GRCm39) |
G364D |
probably benign |
Het |
|
Other mutations in Nutm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00885:Nutm2
|
APN |
13 |
50,628,896 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01087:Nutm2
|
APN |
13 |
50,623,665 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01707:Nutm2
|
APN |
13 |
50,623,753 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02085:Nutm2
|
APN |
13 |
50,627,829 (GRCm39) |
splice site |
probably null |
|
IGL02238:Nutm2
|
APN |
13 |
50,625,075 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02369:Nutm2
|
APN |
13 |
50,623,944 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02429:Nutm2
|
APN |
13 |
50,623,516 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03083:Nutm2
|
APN |
13 |
50,621,480 (GRCm39) |
missense |
probably damaging |
0.98 |
R0233:Nutm2
|
UTSW |
13 |
50,621,441 (GRCm39) |
missense |
probably benign |
0.41 |
R0233:Nutm2
|
UTSW |
13 |
50,621,441 (GRCm39) |
missense |
probably benign |
0.41 |
R0321:Nutm2
|
UTSW |
13 |
50,626,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R1481:Nutm2
|
UTSW |
13 |
50,623,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R1605:Nutm2
|
UTSW |
13 |
50,623,955 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1679:Nutm2
|
UTSW |
13 |
50,623,422 (GRCm39) |
missense |
probably benign |
0.17 |
R1744:Nutm2
|
UTSW |
13 |
50,623,390 (GRCm39) |
missense |
probably benign |
0.03 |
R1768:Nutm2
|
UTSW |
13 |
50,627,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Nutm2
|
UTSW |
13 |
50,627,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R2026:Nutm2
|
UTSW |
13 |
50,628,856 (GRCm39) |
missense |
probably benign |
0.00 |
R2187:Nutm2
|
UTSW |
13 |
50,621,453 (GRCm39) |
missense |
probably benign |
0.00 |
R3912:Nutm2
|
UTSW |
13 |
50,626,976 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4025:Nutm2
|
UTSW |
13 |
50,623,389 (GRCm39) |
missense |
probably benign |
|
R4367:Nutm2
|
UTSW |
13 |
50,623,920 (GRCm39) |
missense |
probably benign |
0.01 |
R4668:Nutm2
|
UTSW |
13 |
50,627,033 (GRCm39) |
missense |
probably benign |
0.18 |
R4940:Nutm2
|
UTSW |
13 |
50,628,909 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4987:Nutm2
|
UTSW |
13 |
50,626,379 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4988:Nutm2
|
UTSW |
13 |
50,626,379 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5821:Nutm2
|
UTSW |
13 |
50,623,891 (GRCm39) |
missense |
probably benign |
0.01 |
R5986:Nutm2
|
UTSW |
13 |
50,628,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R6189:Nutm2
|
UTSW |
13 |
50,623,774 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7101:Nutm2
|
UTSW |
13 |
50,626,934 (GRCm39) |
missense |
probably benign |
0.00 |
R7192:Nutm2
|
UTSW |
13 |
50,627,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R7394:Nutm2
|
UTSW |
13 |
50,624,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R7591:Nutm2
|
UTSW |
13 |
50,627,903 (GRCm39) |
missense |
probably damaging |
0.98 |
R8217:Nutm2
|
UTSW |
13 |
50,623,759 (GRCm39) |
missense |
probably benign |
0.16 |
R8347:Nutm2
|
UTSW |
13 |
50,626,373 (GRCm39) |
missense |
probably benign |
0.05 |
R8811:Nutm2
|
UTSW |
13 |
50,623,989 (GRCm39) |
missense |
probably benign |
0.02 |
R9093:Nutm2
|
UTSW |
13 |
50,628,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R9420:Nutm2
|
UTSW |
13 |
50,626,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R9532:Nutm2
|
UTSW |
13 |
50,628,475 (GRCm39) |
missense |
probably benign |
0.00 |
R9632:Nutm2
|
UTSW |
13 |
50,628,901 (GRCm39) |
missense |
probably benign |
0.10 |
R9650:Nutm2
|
UTSW |
13 |
50,623,755 (GRCm39) |
missense |
probably benign |
0.25 |
R9683:Nutm2
|
UTSW |
13 |
50,629,017 (GRCm39) |
missense |
possibly damaging |
0.92 |
X0028:Nutm2
|
UTSW |
13 |
50,626,990 (GRCm39) |
missense |
probably benign |
0.04 |
|