Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930474N05Rik |
C |
T |
14: 35,818,649 (GRCm39) |
R216C |
probably benign |
Het |
Acsl3 |
C |
T |
1: 78,671,988 (GRCm39) |
P294L |
probably damaging |
Het |
Alox12b |
T |
C |
11: 69,059,663 (GRCm39) |
Y572H |
probably damaging |
Het |
Arid1b |
A |
G |
17: 5,377,959 (GRCm39) |
D1236G |
probably damaging |
Het |
Astl |
T |
C |
2: 127,192,419 (GRCm39) |
L254P |
probably damaging |
Het |
Btbd7 |
A |
C |
12: 102,761,499 (GRCm39) |
L562R |
probably damaging |
Het |
Chl1 |
T |
C |
6: 103,706,250 (GRCm39) |
V1195A |
probably benign |
Het |
Ciao2b |
T |
A |
8: 105,367,668 (GRCm39) |
S94C |
probably damaging |
Het |
Cib1 |
A |
T |
7: 79,878,162 (GRCm39) |
Y105* |
probably null |
Het |
Cog3 |
G |
T |
14: 75,984,533 (GRCm39) |
S94Y |
possibly damaging |
Het |
Cpne6 |
A |
C |
14: 55,753,751 (GRCm39) |
Q403P |
probably damaging |
Het |
Csn1s1 |
A |
G |
5: 87,822,087 (GRCm39) |
N119S |
possibly damaging |
Het |
Cux2 |
T |
C |
5: 122,006,648 (GRCm39) |
D874G |
possibly damaging |
Het |
Dicer1 |
A |
T |
12: 104,670,328 (GRCm39) |
F1079Y |
probably damaging |
Het |
Dsc2 |
T |
A |
18: 20,167,720 (GRCm39) |
Q724H |
possibly damaging |
Het |
Fbxw16 |
A |
G |
9: 109,265,766 (GRCm39) |
V351A |
probably damaging |
Het |
G2e3 |
A |
T |
12: 51,400,624 (GRCm39) |
E59D |
probably benign |
Het |
Gm10800 |
A |
AC |
2: 98,497,378 (GRCm39) |
|
probably null |
Het |
Gm10837 |
G |
T |
14: 122,728,053 (GRCm39) |
|
probably benign |
Het |
Gpr137b |
T |
C |
13: 13,533,991 (GRCm39) |
Y355C |
|
Het |
Gpr18 |
T |
C |
14: 122,149,393 (GRCm39) |
I211V |
probably benign |
Het |
Gstm7 |
T |
A |
3: 107,837,657 (GRCm39) |
D98V |
probably damaging |
Het |
Hspa8 |
A |
G |
9: 40,715,810 (GRCm39) |
Y525C |
probably damaging |
Het |
Itga7 |
T |
C |
10: 128,770,020 (GRCm39) |
S55P |
probably damaging |
Het |
Itpr1 |
T |
C |
6: 108,394,909 (GRCm39) |
V1674A |
possibly damaging |
Het |
Itsn1 |
G |
T |
16: 91,647,824 (GRCm39) |
G893C |
unknown |
Het |
Kcnc1 |
A |
G |
7: 46,047,223 (GRCm39) |
D41G |
probably benign |
Het |
Larp6 |
A |
G |
9: 60,631,638 (GRCm39) |
K137E |
probably damaging |
Het |
Leo1 |
G |
T |
9: 75,352,558 (GRCm39) |
G34C |
probably benign |
Het |
Map4 |
G |
A |
9: 109,908,929 (GRCm39) |
V1050M |
probably damaging |
Het |
Mast3 |
A |
G |
8: 71,236,214 (GRCm39) |
V722A |
probably benign |
Het |
Med28 |
T |
A |
5: 45,682,541 (GRCm39) |
V69D |
probably damaging |
Het |
Mier1 |
T |
C |
4: 103,019,812 (GRCm39) |
F512S |
probably benign |
Het |
Mix23 |
T |
A |
16: 35,905,403 (GRCm39) |
V65D |
probably benign |
Het |
Mov10l1 |
T |
A |
15: 88,937,642 (GRCm39) |
V1147E |
probably damaging |
Het |
Mroh7 |
T |
C |
4: 106,568,478 (GRCm39) |
E409G |
probably benign |
Het |
Muc16 |
G |
T |
9: 18,551,188 (GRCm39) |
P5035Q |
probably benign |
Het |
Npffr2 |
T |
C |
5: 89,731,149 (GRCm39) |
Y360H |
probably damaging |
Het |
Nrxn2 |
T |
C |
19: 6,559,905 (GRCm39) |
V1221A |
probably damaging |
Het |
Nup107 |
A |
G |
10: 117,593,899 (GRCm39) |
F765L |
probably damaging |
Het |
Nup188 |
T |
C |
2: 30,220,983 (GRCm39) |
L991P |
probably damaging |
Het |
Or13f5 |
A |
T |
4: 52,825,970 (GRCm39) |
D191V |
possibly damaging |
Het |
Or5ac23 |
T |
A |
16: 59,149,633 (GRCm39) |
M80L |
probably benign |
Het |
Pla2g7 |
A |
T |
17: 43,922,209 (GRCm39) |
I363L |
probably benign |
Het |
Ppp2r1a |
T |
C |
17: 21,181,901 (GRCm39) |
F473S |
possibly damaging |
Het |
Prex1 |
A |
G |
2: 166,428,965 (GRCm39) |
|
probably null |
Het |
Ptov1 |
A |
G |
7: 44,514,353 (GRCm39) |
V263A |
probably damaging |
Het |
Reg3a |
T |
C |
6: 78,358,132 (GRCm39) |
V21A |
probably benign |
Het |
Sdk2 |
T |
A |
11: 113,750,764 (GRCm39) |
I550F |
probably benign |
Het |
Shprh |
T |
A |
10: 11,061,085 (GRCm39) |
W1133R |
probably damaging |
Het |
Slc28a2b |
T |
C |
2: 122,324,839 (GRCm39) |
L137P |
probably damaging |
Het |
Syne2 |
T |
C |
12: 76,134,632 (GRCm39) |
V1297A |
probably damaging |
Het |
Themis2 |
A |
G |
4: 132,519,875 (GRCm39) |
I50T |
probably damaging |
Het |
Tmprss15 |
C |
A |
16: 78,798,731 (GRCm39) |
L650F |
possibly damaging |
Het |
Ttc41 |
C |
A |
10: 86,572,711 (GRCm39) |
N694K |
probably benign |
Het |
Ttll9 |
T |
C |
2: 152,833,546 (GRCm39) |
Y215H |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,733,653 (GRCm39) |
V4541L |
unknown |
Het |
Usp32 |
G |
T |
11: 84,885,252 (GRCm39) |
A1265E |
probably damaging |
Het |
Vcan |
T |
A |
13: 89,852,446 (GRCm39) |
D838V |
probably damaging |
Het |
Vmn2r88 |
T |
C |
14: 51,651,565 (GRCm39) |
I293T |
|
Het |
Wdr36 |
T |
G |
18: 32,985,572 (GRCm39) |
D496E |
probably damaging |
Het |
Wrn |
T |
C |
8: 33,782,671 (GRCm39) |
N753S |
probably benign |
Het |
Zmat3 |
T |
C |
3: 32,395,815 (GRCm39) |
R231G |
possibly damaging |
Het |
|
Other mutations in Nemp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02172:Nemp1
|
APN |
10 |
127,528,868 (GRCm39) |
missense |
probably benign |
0.02 |
Assassin
|
UTSW |
10 |
127,525,212 (GRCm39) |
nonsense |
probably null |
|
Brightside
|
UTSW |
10 |
127,525,319 (GRCm39) |
splice site |
probably null |
|
Cheery
|
UTSW |
10 |
127,513,067 (GRCm39) |
missense |
possibly damaging |
0.86 |
kidon
|
UTSW |
10 |
127,525,227 (GRCm39) |
missense |
possibly damaging |
0.85 |
PIT4453001:Nemp1
|
UTSW |
10 |
127,532,123 (GRCm39) |
missense |
probably benign |
0.00 |
R0815:Nemp1
|
UTSW |
10 |
127,528,893 (GRCm39) |
missense |
probably damaging |
0.99 |
R1719:Nemp1
|
UTSW |
10 |
127,532,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R2007:Nemp1
|
UTSW |
10 |
127,529,446 (GRCm39) |
missense |
probably benign |
0.02 |
R2042:Nemp1
|
UTSW |
10 |
127,532,203 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3938:Nemp1
|
UTSW |
10 |
127,531,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R4548:Nemp1
|
UTSW |
10 |
127,532,213 (GRCm39) |
missense |
probably benign |
0.00 |
R4726:Nemp1
|
UTSW |
10 |
127,530,462 (GRCm39) |
missense |
probably benign |
0.01 |
R4981:Nemp1
|
UTSW |
10 |
127,529,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R5048:Nemp1
|
UTSW |
10 |
127,526,804 (GRCm39) |
critical splice donor site |
probably null |
|
R5784:Nemp1
|
UTSW |
10 |
127,513,067 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6073:Nemp1
|
UTSW |
10 |
127,525,112 (GRCm39) |
missense |
probably benign |
0.01 |
R6171:Nemp1
|
UTSW |
10 |
127,525,319 (GRCm39) |
splice site |
probably null |
|
R6294:Nemp1
|
UTSW |
10 |
127,530,391 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7249:Nemp1
|
UTSW |
10 |
127,529,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R7269:Nemp1
|
UTSW |
10 |
127,531,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R7316:Nemp1
|
UTSW |
10 |
127,525,212 (GRCm39) |
nonsense |
probably null |
|
R7468:Nemp1
|
UTSW |
10 |
127,528,923 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8342:Nemp1
|
UTSW |
10 |
127,528,898 (GRCm39) |
missense |
probably benign |
0.00 |
R8672:Nemp1
|
UTSW |
10 |
127,512,988 (GRCm39) |
missense |
probably benign |
|
R8756:Nemp1
|
UTSW |
10 |
127,528,845 (GRCm39) |
missense |
probably benign |
0.30 |
R9228:Nemp1
|
UTSW |
10 |
127,525,227 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9749:Nemp1
|
UTSW |
10 |
127,524,198 (GRCm39) |
missense |
probably benign |
0.44 |
X0011:Nemp1
|
UTSW |
10 |
127,525,180 (GRCm39) |
nonsense |
probably null |
|
Z1177:Nemp1
|
UTSW |
10 |
127,529,388 (GRCm39) |
missense |
probably damaging |
0.98 |
|