Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
Areg |
A |
T |
5: 91,291,456 (GRCm39) |
K133M |
probably damaging |
Het |
Atxn2l |
A |
T |
7: 126,091,689 (GRCm39) |
D1076E |
possibly damaging |
Het |
Barhl1 |
T |
C |
2: 28,805,231 (GRCm39) |
Y154C |
probably damaging |
Het |
BC048507 |
A |
G |
13: 68,011,823 (GRCm39) |
T67A |
probably benign |
Het |
Cacna1g |
T |
A |
11: 94,307,491 (GRCm39) |
I1746F |
probably damaging |
Het |
Ccdc34 |
T |
C |
2: 109,874,580 (GRCm39) |
I313T |
possibly damaging |
Het |
Cma1 |
T |
A |
14: 56,179,771 (GRCm39) |
I138F |
probably damaging |
Het |
Col5a2 |
A |
G |
1: 45,542,008 (GRCm39) |
S23P |
unknown |
Het |
Csmd2 |
C |
A |
4: 128,380,658 (GRCm39) |
S2071R |
probably benign |
Het |
Cyp2j11 |
T |
G |
4: 96,233,322 (GRCm39) |
N125H |
probably benign |
Het |
Dchs2 |
A |
G |
3: 83,262,368 (GRCm39) |
R2879G |
possibly damaging |
Het |
Dnah11 |
A |
T |
12: 118,068,586 (GRCm39) |
C1591S |
probably damaging |
Het |
Dock9 |
C |
T |
14: 121,783,385 (GRCm39) |
R2038H |
probably benign |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Fbxo21 |
G |
A |
5: 118,126,948 (GRCm39) |
R233H |
probably damaging |
Het |
Firrm |
T |
C |
1: 163,805,656 (GRCm39) |
Y316C |
probably damaging |
Het |
Gm6526 |
A |
G |
14: 43,986,331 (GRCm39) |
I86V |
probably damaging |
Het |
Gpr107 |
T |
A |
2: 31,042,384 (GRCm39) |
V5E |
probably benign |
Het |
Hat1 |
A |
T |
2: 71,240,585 (GRCm39) |
D93V |
probably benign |
Het |
Kl |
C |
G |
5: 150,876,466 (GRCm39) |
F95L |
probably damaging |
Het |
Lsamp |
A |
G |
16: 41,954,788 (GRCm39) |
K229E |
probably benign |
Het |
Mcm5 |
A |
G |
8: 75,840,825 (GRCm39) |
D210G |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,689,581 (GRCm39) |
V930A |
possibly damaging |
Het |
Megf6 |
T |
A |
4: 154,347,056 (GRCm39) |
C652* |
probably null |
Het |
Nae1 |
A |
T |
8: 105,251,001 (GRCm39) |
L196H |
possibly damaging |
Het |
Ncor1 |
G |
T |
11: 62,208,675 (GRCm39) |
D156E |
probably damaging |
Het |
Nop14 |
A |
T |
5: 34,817,235 (GRCm39) |
V52E |
probably damaging |
Het |
Nova2 |
G |
A |
7: 18,691,794 (GRCm39) |
A244T |
unknown |
Het |
Parp14 |
A |
T |
16: 35,677,389 (GRCm39) |
C860S |
probably damaging |
Het |
Ptpn4 |
T |
C |
1: 119,692,866 (GRCm39) |
Y161C |
probably damaging |
Het |
Ptpn9 |
T |
A |
9: 56,968,430 (GRCm39) |
M590K |
probably benign |
Het |
Ptprq |
A |
G |
10: 107,361,621 (GRCm39) |
I2130T |
probably damaging |
Het |
Pudp |
C |
A |
18: 50,701,299 (GRCm39) |
G145W |
probably damaging |
Het |
Pxk |
A |
G |
14: 8,150,964 (GRCm38) |
K423R |
probably benign |
Het |
Ryr1 |
A |
G |
7: 28,786,863 (GRCm39) |
S1584P |
probably damaging |
Het |
Scap |
G |
A |
9: 110,207,845 (GRCm39) |
R518H |
probably damaging |
Het |
Slc5a12 |
T |
C |
2: 110,447,092 (GRCm39) |
L200P |
probably damaging |
Het |
Sntg1 |
T |
A |
1: 8,749,338 (GRCm39) |
*72Y |
probably null |
Het |
Speer4f1 |
A |
C |
5: 17,684,482 (GRCm39) |
Q170P |
possibly damaging |
Het |
Taar7d |
A |
C |
10: 23,903,558 (GRCm39) |
I147L |
probably benign |
Het |
Tet2 |
T |
C |
3: 133,177,196 (GRCm39) |
K1284E |
possibly damaging |
Het |
Trpm2 |
A |
C |
10: 77,770,877 (GRCm39) |
|
probably null |
Het |
Washc2 |
T |
A |
6: 116,204,327 (GRCm39) |
S412T |
probably benign |
Het |
Zfyve26 |
A |
G |
12: 79,340,628 (GRCm39) |
V82A |
possibly damaging |
Het |
|
Other mutations in Kctd21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01358:Kctd21
|
APN |
7 |
96,996,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R0123:Kctd21
|
UTSW |
7 |
96,997,298 (GRCm39) |
missense |
probably benign |
0.04 |
R0134:Kctd21
|
UTSW |
7 |
96,997,298 (GRCm39) |
missense |
probably benign |
0.04 |
R0225:Kctd21
|
UTSW |
7 |
96,997,298 (GRCm39) |
missense |
probably benign |
0.04 |
R0469:Kctd21
|
UTSW |
7 |
96,996,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0510:Kctd21
|
UTSW |
7 |
96,996,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0606:Kctd21
|
UTSW |
7 |
96,996,808 (GRCm39) |
missense |
probably benign |
0.01 |
R1438:Kctd21
|
UTSW |
7 |
96,996,704 (GRCm39) |
missense |
probably damaging |
0.98 |
R4625:Kctd21
|
UTSW |
7 |
96,996,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R4626:Kctd21
|
UTSW |
7 |
96,996,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R4628:Kctd21
|
UTSW |
7 |
96,996,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R4629:Kctd21
|
UTSW |
7 |
96,996,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R5348:Kctd21
|
UTSW |
7 |
96,997,177 (GRCm39) |
missense |
probably benign |
0.33 |
R6452:Kctd21
|
UTSW |
7 |
96,996,869 (GRCm39) |
missense |
probably benign |
0.04 |
R6736:Kctd21
|
UTSW |
7 |
96,997,291 (GRCm39) |
missense |
probably damaging |
0.99 |
R7402:Kctd21
|
UTSW |
7 |
96,996,970 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7782:Kctd21
|
UTSW |
7 |
96,997,297 (GRCm39) |
missense |
probably benign |
|
R8214:Kctd21
|
UTSW |
7 |
96,996,548 (GRCm39) |
missense |
probably damaging |
1.00 |
|