Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
T |
C |
8: 87,275,388 (GRCm39) |
D430G |
probably damaging |
Het |
Adgrf1 |
T |
C |
17: 43,621,580 (GRCm39) |
S606P |
possibly damaging |
Het |
Afap1 |
A |
G |
5: 36,141,540 (GRCm39) |
N475D |
probably damaging |
Het |
Ahnak2 |
A |
G |
12: 112,739,468 (GRCm39) |
S1535P |
possibly damaging |
Het |
Akt1 |
G |
T |
12: 112,624,885 (GRCm39) |
H194N |
possibly damaging |
Het |
Api5 |
T |
A |
2: 94,251,812 (GRCm39) |
Q396L |
possibly damaging |
Het |
Aplp2 |
T |
C |
9: 31,083,303 (GRCm39) |
N148S |
probably benign |
Het |
Asb3 |
A |
G |
11: 31,031,400 (GRCm39) |
Y340C |
probably damaging |
Het |
Bbox1 |
A |
T |
2: 110,098,581 (GRCm39) |
M332K |
probably damaging |
Het |
Cabin1 |
A |
T |
10: 75,579,090 (GRCm39) |
S449T |
probably benign |
Het |
Carns1 |
A |
G |
19: 4,216,007 (GRCm39) |
V725A |
possibly damaging |
Het |
Cdkn1b |
A |
G |
6: 134,898,058 (GRCm39) |
K59R |
possibly damaging |
Het |
Cdv3 |
A |
T |
9: 103,233,539 (GRCm39) |
I212K |
probably damaging |
Het |
Clec14a |
T |
A |
12: 58,314,432 (GRCm39) |
I397F |
probably damaging |
Het |
Cnnm1 |
A |
G |
19: 43,483,469 (GRCm39) |
I950V |
possibly damaging |
Het |
Ddi2 |
A |
G |
4: 141,422,734 (GRCm39) |
M326T |
probably benign |
Het |
Dhx30 |
T |
C |
9: 109,914,103 (GRCm39) |
T1065A |
probably benign |
Het |
Eif3c |
A |
T |
7: 126,146,674 (GRCm39) |
M808K |
possibly damaging |
Het |
Evi2 |
G |
T |
11: 79,406,971 (GRCm39) |
H201Q |
possibly damaging |
Het |
Exoc4 |
A |
G |
6: 33,452,991 (GRCm39) |
T494A |
unknown |
Het |
Fam83f |
T |
A |
15: 80,574,819 (GRCm39) |
M242K |
probably damaging |
Het |
Fat4 |
T |
C |
3: 39,055,374 (GRCm39) |
Y4198H |
probably benign |
Het |
Fcgbp |
C |
A |
7: 27,793,000 (GRCm39) |
N1001K |
probably benign |
Het |
Gda |
G |
T |
19: 21,400,449 (GRCm39) |
A164E |
probably damaging |
Het |
Gm19410 |
T |
C |
8: 36,279,493 (GRCm39) |
V1786A |
possibly damaging |
Het |
Gm45871 |
A |
G |
18: 90,609,069 (GRCm39) |
N82S |
probably benign |
Het |
Gnas |
T |
A |
2: 174,141,392 (GRCm39) |
S580T |
unknown |
Het |
Gprin1 |
G |
A |
13: 54,886,714 (GRCm39) |
P520L |
probably benign |
Het |
Gramd4 |
C |
T |
15: 86,014,751 (GRCm39) |
R433C |
probably damaging |
Het |
Ighv5-12 |
T |
A |
12: 113,665,958 (GRCm39) |
T47S |
probably benign |
Het |
Itprid1 |
T |
G |
6: 55,864,018 (GRCm39) |
S115A |
probably damaging |
Het |
Kdm5a |
T |
A |
6: 120,367,658 (GRCm39) |
L451Q |
probably damaging |
Het |
Kif12 |
T |
A |
4: 63,084,126 (GRCm39) |
R624S |
probably benign |
Het |
Lepr |
T |
A |
4: 101,592,851 (GRCm39) |
Y155* |
probably null |
Het |
Lnx2 |
T |
A |
5: 146,961,376 (GRCm39) |
I519F |
probably damaging |
Het |
Marchf7 |
T |
A |
2: 60,060,175 (GRCm39) |
S101T |
probably damaging |
Het |
Miox |
A |
G |
15: 89,220,785 (GRCm39) |
D230G |
probably damaging |
Het |
Morc2a |
T |
A |
11: 3,600,381 (GRCm39) |
M1K |
probably null |
Het |
Mtus1 |
T |
C |
8: 41,536,222 (GRCm39) |
N498S |
probably damaging |
Het |
Mxd1 |
T |
A |
6: 86,645,554 (GRCm39) |
R46W |
probably damaging |
Het |
Ndufa11 |
G |
C |
17: 57,024,843 (GRCm39) |
A2P |
possibly damaging |
Het |
Necab2 |
C |
T |
8: 120,198,513 (GRCm39) |
H362Y |
probably damaging |
Het |
Nphp4 |
G |
A |
4: 152,623,434 (GRCm39) |
V703I |
possibly damaging |
Het |
Nup54 |
T |
C |
5: 92,582,218 (GRCm39) |
N31S |
unknown |
Het |
Or13a23-ps1 |
T |
A |
7: 140,118,497 (GRCm39) |
S22R |
probably benign |
Het |
Or1ad6 |
T |
C |
11: 50,860,316 (GRCm39) |
L157P |
probably damaging |
Het |
Or1e34 |
A |
T |
11: 73,778,696 (GRCm39) |
C167* |
probably null |
Het |
Or8b4 |
A |
C |
9: 37,830,066 (GRCm39) |
T38P |
probably damaging |
Het |
P2rx2 |
T |
C |
5: 110,490,388 (GRCm39) |
E109G |
possibly damaging |
Het |
Pcdha7 |
T |
C |
18: 37,107,409 (GRCm39) |
S145P |
probably damaging |
Het |
Pdlim5 |
A |
T |
3: 141,948,529 (GRCm39) |
V586E |
probably damaging |
Het |
Pex5l |
T |
C |
3: 33,136,204 (GRCm39) |
E5G |
probably benign |
Het |
Plch1 |
T |
A |
3: 63,615,176 (GRCm39) |
D774V |
probably damaging |
Het |
Plekhg3 |
A |
T |
12: 76,611,726 (GRCm39) |
D335V |
possibly damaging |
Het |
Pop1 |
A |
G |
15: 34,530,227 (GRCm39) |
H905R |
probably benign |
Het |
Ppm1k |
T |
C |
6: 57,492,720 (GRCm39) |
T189A |
probably damaging |
Het |
Pramel13 |
A |
G |
4: 144,122,517 (GRCm39) |
L9P |
probably damaging |
Het |
Recql5 |
A |
G |
11: 115,784,367 (GRCm39) |
V911A |
probably damaging |
Het |
Rnf145 |
T |
A |
11: 44,415,830 (GRCm39) |
L15* |
probably null |
Het |
Rpl13a |
A |
G |
7: 44,776,673 (GRCm39) |
V29A |
probably benign |
Het |
Rps6ka5 |
A |
G |
12: 100,540,250 (GRCm39) |
V491A |
probably benign |
Het |
Setbp1 |
T |
C |
18: 78,900,142 (GRCm39) |
H1175R |
probably benign |
Het |
Slc1a3 |
T |
C |
15: 8,675,177 (GRCm39) |
E276G |
probably damaging |
Het |
Slc36a2 |
T |
C |
11: 55,070,169 (GRCm39) |
N136S |
probably benign |
Het |
Spag1 |
G |
A |
15: 36,190,683 (GRCm39) |
|
probably null |
Het |
Spon1 |
A |
C |
7: 113,387,685 (GRCm39) |
T81P |
probably damaging |
Het |
Sv2b |
A |
T |
7: 74,856,238 (GRCm39) |
D17E |
probably benign |
Het |
Tasor2 |
A |
G |
13: 3,649,667 (GRCm39) |
V44A |
probably benign |
Het |
Tax1bp1 |
C |
T |
6: 52,704,215 (GRCm39) |
T65I |
probably damaging |
Het |
Tenm2 |
C |
A |
11: 35,915,341 (GRCm39) |
K2065N |
probably damaging |
Het |
Ticam2 |
T |
C |
18: 46,693,658 (GRCm39) |
D143G |
probably damaging |
Het |
Tmem132d |
T |
C |
5: 127,869,579 (GRCm39) |
E585G |
possibly damaging |
Het |
Tnfrsf8 |
C |
T |
4: 145,019,668 (GRCm39) |
|
probably null |
Het |
Trim44 |
C |
T |
2: 102,230,813 (GRCm39) |
G73R |
unknown |
Het |
Trpc3 |
C |
T |
3: 36,692,713 (GRCm39) |
D760N |
possibly damaging |
Het |
Tspan9 |
T |
A |
6: 127,942,715 (GRCm39) |
M171L |
probably benign |
Het |
Ugt2b37 |
A |
G |
5: 87,402,532 (GRCm39) |
F33S |
possibly damaging |
Het |
Vav2 |
A |
T |
2: 27,159,027 (GRCm39) |
V734E |
probably damaging |
Het |
Vmn1r214 |
A |
G |
13: 23,218,508 (GRCm39) |
M1V |
probably null |
Het |
Vmn1r24 |
A |
T |
6: 57,932,804 (GRCm39) |
V238E |
probably damaging |
Het |
Vmn2r107 |
A |
G |
17: 20,577,262 (GRCm39) |
Q420R |
probably damaging |
Het |
Vmn2r31 |
G |
A |
7: 7,387,085 (GRCm39) |
P829S |
probably damaging |
Het |
Xpo6 |
A |
G |
7: 125,712,873 (GRCm39) |
F703L |
probably benign |
Het |
Zfp442 |
T |
A |
2: 150,250,207 (GRCm39) |
H565L |
possibly damaging |
Het |
Zfp950 |
A |
T |
19: 61,116,000 (GRCm39) |
D2E |
probably damaging |
Het |
Zfp992 |
T |
A |
4: 146,551,345 (GRCm39) |
S355R |
probably damaging |
Het |
Zwilch |
A |
T |
9: 64,063,303 (GRCm39) |
F309Y |
probably damaging |
Het |
|
Other mutations in Setd5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00816:Setd5
|
APN |
6 |
113,088,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02102:Setd5
|
APN |
6 |
113,127,946 (GRCm39) |
nonsense |
probably null |
|
IGL02105:Setd5
|
APN |
6 |
113,094,541 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02202:Setd5
|
APN |
6 |
113,127,976 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02221:Setd5
|
APN |
6 |
113,098,131 (GRCm39) |
splice site |
probably benign |
|
IGL02382:Setd5
|
APN |
6 |
113,120,601 (GRCm39) |
missense |
probably benign |
|
IGL02394:Setd5
|
APN |
6 |
113,087,859 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02442:Setd5
|
APN |
6 |
113,087,341 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02480:Setd5
|
APN |
6 |
113,120,770 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02940:Setd5
|
APN |
6 |
113,091,899 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0320:Setd5
|
UTSW |
6 |
113,088,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R0479:Setd5
|
UTSW |
6 |
113,091,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R0514:Setd5
|
UTSW |
6 |
113,096,398 (GRCm39) |
nonsense |
probably null |
|
R1528:Setd5
|
UTSW |
6 |
113,098,699 (GRCm39) |
missense |
probably damaging |
0.99 |
R1530:Setd5
|
UTSW |
6 |
113,086,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R2176:Setd5
|
UTSW |
6 |
113,128,114 (GRCm39) |
missense |
probably benign |
0.23 |
R2191:Setd5
|
UTSW |
6 |
113,088,390 (GRCm39) |
nonsense |
probably null |
|
R2286:Setd5
|
UTSW |
6 |
113,096,571 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4163:Setd5
|
UTSW |
6 |
113,096,545 (GRCm39) |
missense |
probably benign |
|
R4294:Setd5
|
UTSW |
6 |
113,088,281 (GRCm39) |
intron |
probably benign |
|
R4300:Setd5
|
UTSW |
6 |
113,127,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R4342:Setd5
|
UTSW |
6 |
113,088,281 (GRCm39) |
intron |
probably benign |
|
R4370:Setd5
|
UTSW |
6 |
113,098,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R4854:Setd5
|
UTSW |
6 |
113,128,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R4858:Setd5
|
UTSW |
6 |
113,126,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Setd5
|
UTSW |
6 |
113,114,922 (GRCm39) |
missense |
probably damaging |
0.96 |
R5345:Setd5
|
UTSW |
6 |
113,092,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R5529:Setd5
|
UTSW |
6 |
113,098,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R5556:Setd5
|
UTSW |
6 |
113,124,463 (GRCm39) |
missense |
probably benign |
0.00 |
R5582:Setd5
|
UTSW |
6 |
113,091,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R5838:Setd5
|
UTSW |
6 |
113,096,396 (GRCm39) |
missense |
probably benign |
0.40 |
R5941:Setd5
|
UTSW |
6 |
113,105,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R6009:Setd5
|
UTSW |
6 |
113,087,480 (GRCm39) |
missense |
probably damaging |
0.99 |
R6146:Setd5
|
UTSW |
6 |
113,098,773 (GRCm39) |
critical splice donor site |
probably null |
|
R6394:Setd5
|
UTSW |
6 |
113,092,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R6694:Setd5
|
UTSW |
6 |
113,120,669 (GRCm39) |
missense |
probably benign |
|
R7058:Setd5
|
UTSW |
6 |
113,092,532 (GRCm39) |
missense |
probably benign |
0.16 |
R7060:Setd5
|
UTSW |
6 |
113,094,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7199:Setd5
|
UTSW |
6 |
113,098,099 (GRCm39) |
missense |
probably benign |
0.03 |
R7238:Setd5
|
UTSW |
6 |
113,098,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R7296:Setd5
|
UTSW |
6 |
113,124,518 (GRCm39) |
missense |
probably benign |
0.21 |
R7438:Setd5
|
UTSW |
6 |
113,092,043 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7515:Setd5
|
UTSW |
6 |
113,087,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R7621:Setd5
|
UTSW |
6 |
113,121,010 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7652:Setd5
|
UTSW |
6 |
113,098,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7986:Setd5
|
UTSW |
6 |
113,105,418 (GRCm39) |
missense |
probably benign |
0.00 |
R8083:Setd5
|
UTSW |
6 |
113,091,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R8175:Setd5
|
UTSW |
6 |
113,091,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R8252:Setd5
|
UTSW |
6 |
113,127,916 (GRCm39) |
missense |
probably benign |
0.01 |
R8268:Setd5
|
UTSW |
6 |
113,126,651 (GRCm39) |
critical splice donor site |
probably null |
|
R8271:Setd5
|
UTSW |
6 |
113,092,031 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8424:Setd5
|
UTSW |
6 |
113,126,644 (GRCm39) |
missense |
probably benign |
0.12 |
R8508:Setd5
|
UTSW |
6 |
113,098,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R8801:Setd5
|
UTSW |
6 |
113,127,853 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8864:Setd5
|
UTSW |
6 |
113,088,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R9227:Setd5
|
UTSW |
6 |
113,098,755 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9522:Setd5
|
UTSW |
6 |
113,091,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R9588:Setd5
|
UTSW |
6 |
113,121,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Setd5
|
UTSW |
6 |
113,128,366 (GRCm39) |
missense |
probably benign |
0.13 |
R9728:Setd5
|
UTSW |
6 |
113,128,366 (GRCm39) |
missense |
probably benign |
0.13 |
X0017:Setd5
|
UTSW |
6 |
113,127,129 (GRCm39) |
missense |
probably null |
1.00 |
Z1176:Setd5
|
UTSW |
6 |
113,115,057 (GRCm39) |
missense |
probably benign |
|
Z1191:Setd5
|
UTSW |
6 |
113,091,957 (GRCm39) |
missense |
probably benign |
0.04 |
|