Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
C |
T |
3: 124,200,095 (GRCm39) |
G499D |
probably benign |
Het |
Acr |
T |
A |
15: 89,457,440 (GRCm39) |
Y229* |
probably null |
Het |
Adam6b |
G |
T |
12: 113,454,176 (GRCm39) |
C331F |
probably benign |
Het |
Ahnak |
T |
C |
19: 8,984,719 (GRCm39) |
V2001A |
possibly damaging |
Het |
Ankrd11 |
C |
T |
8: 123,617,682 (GRCm39) |
A2057T |
probably benign |
Het |
Anln |
A |
T |
9: 22,283,536 (GRCm39) |
C432* |
probably null |
Het |
Aox4 |
T |
C |
1: 58,278,462 (GRCm39) |
|
probably null |
Het |
Astn1 |
A |
G |
1: 158,491,619 (GRCm39) |
I1007V |
possibly damaging |
Het |
Bicral |
T |
C |
17: 47,122,944 (GRCm39) |
D649G |
possibly damaging |
Het |
C1qbp |
G |
A |
11: 70,873,749 (GRCm39) |
R10C |
probably damaging |
Het |
Cass4 |
C |
T |
2: 172,268,656 (GRCm39) |
P246L |
probably damaging |
Het |
Celsr3 |
T |
A |
9: 108,704,522 (GRCm39) |
V335E |
probably damaging |
Het |
Cfap52 |
T |
A |
11: 67,822,639 (GRCm39) |
T411S |
probably benign |
Het |
Cnot6 |
A |
T |
11: 49,580,164 (GRCm39) |
L43I |
possibly damaging |
Het |
Col9a3 |
G |
A |
2: 180,248,322 (GRCm39) |
|
probably null |
Het |
Dnah14 |
A |
G |
1: 181,426,509 (GRCm39) |
R210G |
probably benign |
Het |
Fat4 |
A |
G |
3: 38,943,332 (GRCm39) |
S742G |
possibly damaging |
Het |
Fbn2 |
C |
T |
18: 58,186,099 (GRCm39) |
V1750M |
probably benign |
Het |
Glrx2 |
A |
G |
1: 143,622,292 (GRCm39) |
D96G |
probably damaging |
Het |
Gm8369 |
T |
C |
19: 11,489,097 (GRCm39) |
L128P |
probably damaging |
Het |
Gpr155 |
A |
G |
2: 73,192,780 (GRCm39) |
I585T |
probably benign |
Het |
Heatr1 |
T |
C |
13: 12,449,140 (GRCm39) |
S1907P |
probably damaging |
Het |
Hscb |
T |
C |
5: 110,983,881 (GRCm39) |
T129A |
possibly damaging |
Het |
Itgb5 |
T |
A |
16: 33,740,335 (GRCm39) |
Y482N |
probably damaging |
Het |
Kmt5b |
T |
A |
19: 3,865,587 (GRCm39) |
*884R |
probably null |
Het |
L3mbtl1 |
A |
T |
2: 162,812,228 (GRCm39) |
T758S |
possibly damaging |
Het |
Mindy1 |
A |
T |
3: 95,202,176 (GRCm39) |
H351L |
probably benign |
Het |
Mmel1 |
A |
T |
4: 154,977,285 (GRCm39) |
I552F |
probably damaging |
Het |
Mos |
T |
C |
4: 3,871,186 (GRCm39) |
D210G |
probably benign |
Het |
Npl |
A |
C |
1: 153,421,030 (GRCm39) |
I16S |
possibly damaging |
Het |
Or1e1c |
G |
A |
11: 73,265,811 (GRCm39) |
V82I |
probably damaging |
Het |
Or52ae7 |
A |
G |
7: 103,119,157 (GRCm39) |
|
probably benign |
Het |
Plekhg4 |
T |
C |
8: 106,102,923 (GRCm39) |
F261L |
probably benign |
Het |
Ppfia3 |
T |
A |
7: 45,005,999 (GRCm39) |
N331I |
probably benign |
Het |
Ppp1r12a |
T |
A |
10: 108,096,747 (GRCm39) |
S712R |
possibly damaging |
Het |
Psg20 |
T |
A |
7: 18,416,508 (GRCm39) |
K203* |
probably null |
Het |
Recql |
C |
T |
6: 142,305,646 (GRCm39) |
R234Q |
|
Het |
Rerg |
A |
G |
6: 137,033,252 (GRCm39) |
F160S |
probably damaging |
Het |
Rp1l1 |
A |
G |
14: 64,269,126 (GRCm39) |
K1571E |
probably damaging |
Het |
Rsrc1 |
T |
A |
3: 67,257,328 (GRCm39) |
S247T |
probably damaging |
Het |
Sacs |
T |
A |
14: 61,450,881 (GRCm39) |
I4309N |
possibly damaging |
Het |
Setd7 |
A |
T |
3: 51,450,111 (GRCm39) |
I105N |
possibly damaging |
Het |
Sgk1 |
AAGA |
AAGAGA |
10: 21,868,290 (GRCm39) |
|
probably null |
Het |
Siglec1 |
T |
A |
2: 130,921,236 (GRCm39) |
H645L |
probably damaging |
Het |
Slain1 |
A |
T |
14: 103,925,621 (GRCm39) |
D323V |
probably damaging |
Het |
Slc25a10 |
A |
G |
11: 120,386,312 (GRCm39) |
N139D |
probably damaging |
Het |
Slc9a9 |
T |
G |
9: 94,552,235 (GRCm39) |
F41V |
probably damaging |
Het |
Spag9 |
A |
C |
11: 93,988,568 (GRCm39) |
E879D |
probably damaging |
Het |
Tdrd7 |
T |
A |
4: 46,025,946 (GRCm39) |
L922Q |
probably damaging |
Het |
Tiprl |
A |
G |
1: 165,050,147 (GRCm39) |
F156S |
probably damaging |
Het |
Tmem185b |
G |
C |
1: 119,454,748 (GRCm39) |
V170L |
probably damaging |
Het |
Top2a |
G |
A |
11: 98,887,683 (GRCm39) |
T1275I |
probably benign |
Het |
Tpp1 |
A |
G |
7: 105,398,104 (GRCm39) |
L353P |
probably damaging |
Het |
Twnk |
T |
A |
19: 44,998,622 (GRCm39) |
H513Q |
probably damaging |
Het |
Ubr5 |
C |
T |
15: 37,978,271 (GRCm39) |
V2467I |
|
Het |
Vmn2r16 |
T |
A |
5: 109,511,677 (GRCm39) |
I628N |
probably damaging |
Het |
Zan |
T |
C |
5: 137,462,776 (GRCm39) |
E801G |
unknown |
Het |
Zfp810 |
T |
C |
9: 22,189,799 (GRCm39) |
R370G |
possibly damaging |
Het |
Zfp955a |
A |
G |
17: 33,461,587 (GRCm39) |
S182P |
probably benign |
Het |
Znrf3 |
T |
C |
11: 5,394,465 (GRCm39) |
T72A |
possibly damaging |
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 |
R9507:Nutm2
|
UTSW |
13 |
50,621,455 (GRCm39) |
missense |
probably benign |
|
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 |
X0028:Nutm2
|
UTSW |
13 |
50,626,990 (GRCm39) |
missense |
probably benign |
0.04 |
|