Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl2 |
T |
C |
3: 148,533,190 (GRCm39) |
T35A |
|
Het |
Adgrv1 |
C |
T |
13: 81,593,462 (GRCm39) |
R4175H |
probably damaging |
Het |
Akt3 |
T |
C |
1: 176,877,611 (GRCm39) |
N386D |
possibly damaging |
Het |
Aox1 |
A |
T |
1: 58,335,046 (GRCm39) |
H282L |
probably benign |
Het |
Asb7 |
G |
T |
7: 66,309,675 (GRCm39) |
N180K |
possibly damaging |
Het |
Cdh23 |
T |
C |
10: 60,274,591 (GRCm39) |
S500G |
possibly damaging |
Het |
Cubn |
C |
T |
2: 13,311,274 (GRCm39) |
E3084K |
probably benign |
Het |
Cyp2r1 |
G |
A |
7: 114,152,405 (GRCm39) |
T184I |
probably damaging |
Het |
Dclk3 |
A |
G |
9: 111,296,602 (GRCm39) |
R49G |
probably damaging |
Het |
Dcp1a |
C |
T |
14: 30,241,527 (GRCm39) |
Q446* |
probably null |
Het |
Dnah9 |
A |
G |
11: 66,008,452 (GRCm39) |
I791T |
probably benign |
Het |
Dock10 |
A |
T |
1: 80,583,892 (GRCm39) |
V189D |
possibly damaging |
Het |
Dsg4 |
A |
G |
18: 20,582,788 (GRCm39) |
E142G |
probably benign |
Het |
Dsp |
A |
T |
13: 38,375,611 (GRCm39) |
D1132V |
probably damaging |
Het |
Dync2h1 |
A |
G |
9: 7,147,771 (GRCm39) |
M953T |
probably benign |
Het |
Ecpas |
G |
T |
4: 58,847,093 (GRCm39) |
Q490K |
probably damaging |
Het |
Ero1a |
T |
C |
14: 45,531,805 (GRCm39) |
H251R |
probably damaging |
Het |
Fer1l5 |
A |
G |
1: 36,415,841 (GRCm39) |
Y124C |
probably benign |
Het |
Frmpd2 |
C |
A |
14: 33,232,992 (GRCm39) |
P404Q |
probably damaging |
Het |
Gpr87 |
G |
T |
3: 59,102,395 (GRCm39) |
|
probably benign |
Het |
Gse1 |
T |
C |
8: 121,305,319 (GRCm39) |
Y1217H |
unknown |
Het |
Heatr5a |
AGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGTGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGAGCACACTGCAGGAAGCTCA |
AGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGAGCACACTGCAGGAAGCTCA |
12: 51,934,702 (GRCm39) |
|
probably benign |
Het |
Irf9 |
T |
A |
14: 55,843,210 (GRCm39) |
D137E |
probably benign |
Het |
Jup |
G |
T |
11: 100,272,571 (GRCm39) |
N280K |
probably benign |
Het |
Kcna7 |
T |
C |
7: 45,058,765 (GRCm39) |
F351L |
probably damaging |
Het |
Klk13 |
A |
T |
7: 43,376,136 (GRCm39) |
R270S |
probably benign |
Het |
Msh6 |
C |
T |
17: 88,294,340 (GRCm39) |
R1032C |
probably damaging |
Het |
Myo5a |
T |
C |
9: 75,125,271 (GRCm39) |
V1855A |
probably damaging |
Het |
Neb |
T |
C |
2: 52,111,714 (GRCm39) |
T138A |
probably damaging |
Het |
Nfkbie |
C |
A |
17: 45,870,234 (GRCm39) |
T193K |
probably damaging |
Het |
Nlrp4b |
A |
G |
7: 10,452,471 (GRCm39) |
K613E |
probably benign |
Het |
Obox6 |
T |
C |
7: 15,567,481 (GRCm39) |
E322G |
possibly damaging |
Het |
Or51ai2 |
A |
G |
7: 103,586,809 (GRCm39) |
D74G |
probably damaging |
Het |
Or5v1b |
T |
G |
17: 37,841,470 (GRCm39) |
S201A |
probably benign |
Het |
Or8b36 |
T |
C |
9: 37,938,014 (GRCm39) |
M304T |
probably benign |
Het |
Parn |
A |
T |
16: 13,483,835 (GRCm39) |
N36K |
probably benign |
Het |
Ppp6r2 |
A |
G |
15: 89,164,650 (GRCm39) |
E618G |
probably benign |
Het |
Prkaa2 |
T |
C |
4: 104,893,495 (GRCm39) |
T485A |
possibly damaging |
Het |
Prmt2 |
G |
T |
10: 76,053,247 (GRCm39) |
T256K |
probably benign |
Het |
Rspry1 |
T |
C |
8: 95,366,217 (GRCm39) |
Y362H |
probably damaging |
Het |
Slc16a14 |
A |
T |
1: 84,890,066 (GRCm39) |
I413N |
possibly damaging |
Het |
Slc8a1 |
T |
C |
17: 81,715,535 (GRCm39) |
T821A |
probably damaging |
Het |
Spock2 |
A |
T |
10: 59,962,777 (GRCm39) |
K276N |
probably damaging |
Het |
Synj1 |
A |
T |
16: 90,785,084 (GRCm39) |
N257K |
probably benign |
Het |
Taar7f |
T |
C |
10: 23,925,811 (GRCm39) |
L135P |
possibly damaging |
Het |
Tmem132b |
T |
C |
5: 125,864,618 (GRCm39) |
F908S |
probably damaging |
Het |
Tmem202 |
A |
T |
9: 59,426,500 (GRCm39) |
V222D |
probably benign |
Het |
Trim33 |
T |
A |
3: 103,218,770 (GRCm39) |
C302* |
probably null |
Het |
Tuba4a |
G |
A |
1: 75,195,265 (GRCm39) |
S1L |
|
Het |
Tyrp1 |
G |
A |
4: 80,768,921 (GRCm39) |
E472K |
probably benign |
Het |
V1ra8 |
A |
G |
6: 90,180,246 (GRCm39) |
I150V |
possibly damaging |
Het |
Vmn2r87 |
A |
T |
10: 130,308,180 (GRCm39) |
M686K |
possibly damaging |
Het |
Zscan5b |
C |
T |
7: 6,236,946 (GRCm39) |
P232S |
possibly damaging |
Het |
|
Other mutations in Prdm13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02940:Prdm13
|
APN |
4 |
21,683,421 (GRCm39) |
nonsense |
probably null |
|
IGL03211:Prdm13
|
APN |
4 |
21,678,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R0363:Prdm13
|
UTSW |
4 |
21,679,737 (GRCm39) |
missense |
unknown |
|
R0512:Prdm13
|
UTSW |
4 |
21,678,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R0726:Prdm13
|
UTSW |
4 |
21,683,914 (GRCm39) |
missense |
unknown |
|
R1056:Prdm13
|
UTSW |
4 |
21,678,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R1433:Prdm13
|
UTSW |
4 |
21,678,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R2005:Prdm13
|
UTSW |
4 |
21,685,695 (GRCm39) |
utr 5 prime |
probably benign |
|
R2292:Prdm13
|
UTSW |
4 |
21,683,914 (GRCm39) |
missense |
unknown |
|
R2382:Prdm13
|
UTSW |
4 |
21,678,277 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3620:Prdm13
|
UTSW |
4 |
21,683,532 (GRCm39) |
missense |
unknown |
|
R4039:Prdm13
|
UTSW |
4 |
21,685,774 (GRCm39) |
utr 5 prime |
probably benign |
|
R4417:Prdm13
|
UTSW |
4 |
21,678,756 (GRCm39) |
missense |
probably benign |
0.39 |
R4453:Prdm13
|
UTSW |
4 |
21,679,464 (GRCm39) |
missense |
unknown |
|
R4850:Prdm13
|
UTSW |
4 |
21,678,243 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4864:Prdm13
|
UTSW |
4 |
21,685,543 (GRCm39) |
missense |
unknown |
|
R4934:Prdm13
|
UTSW |
4 |
21,678,223 (GRCm39) |
utr 3 prime |
probably benign |
|
R5138:Prdm13
|
UTSW |
4 |
21,679,507 (GRCm39) |
missense |
unknown |
|
R5304:Prdm13
|
UTSW |
4 |
21,678,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R5394:Prdm13
|
UTSW |
4 |
21,679,455 (GRCm39) |
missense |
unknown |
|
R5909:Prdm13
|
UTSW |
4 |
21,683,894 (GRCm39) |
missense |
unknown |
|
R5964:Prdm13
|
UTSW |
4 |
21,683,852 (GRCm39) |
nonsense |
probably null |
|
R6261:Prdm13
|
UTSW |
4 |
21,678,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R7166:Prdm13
|
UTSW |
4 |
21,683,528 (GRCm39) |
missense |
unknown |
|
R7175:Prdm13
|
UTSW |
4 |
21,679,473 (GRCm39) |
missense |
unknown |
|
R7549:Prdm13
|
UTSW |
4 |
21,679,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R7966:Prdm13
|
UTSW |
4 |
21,679,932 (GRCm39) |
missense |
unknown |
|
R8319:Prdm13
|
UTSW |
4 |
21,679,327 (GRCm39) |
missense |
unknown |
|
R8701:Prdm13
|
UTSW |
4 |
21,678,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R8924:Prdm13
|
UTSW |
4 |
21,679,125 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8947:Prdm13
|
UTSW |
4 |
21,678,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R9165:Prdm13
|
UTSW |
4 |
21,679,659 (GRCm39) |
missense |
unknown |
|
R9168:Prdm13
|
UTSW |
4 |
21,679,659 (GRCm39) |
missense |
unknown |
|
R9170:Prdm13
|
UTSW |
4 |
21,679,659 (GRCm39) |
missense |
unknown |
|
R9171:Prdm13
|
UTSW |
4 |
21,679,659 (GRCm39) |
missense |
unknown |
|
Z1176:Prdm13
|
UTSW |
4 |
21,679,518 (GRCm39) |
missense |
unknown |
|
Z1177:Prdm13
|
UTSW |
4 |
21,679,623 (GRCm39) |
missense |
unknown |
|
|