Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700128F08Rik |
A |
G |
9: 8,222,066 (GRCm39) |
|
noncoding transcript |
Het |
Aars1 |
A |
G |
8: 111,770,311 (GRCm39) |
M370V |
probably benign |
Het |
Abca2 |
A |
G |
2: 25,328,383 (GRCm39) |
K846R |
probably damaging |
Het |
Acad9 |
A |
T |
3: 36,139,674 (GRCm39) |
I425F |
probably damaging |
Het |
Adhfe1 |
C |
A |
1: 9,628,463 (GRCm39) |
D278E |
possibly damaging |
Het |
Afg3l1 |
G |
A |
8: 124,225,392 (GRCm39) |
V532I |
probably benign |
Het |
Anks6 |
C |
T |
4: 47,030,795 (GRCm39) |
G601S |
probably damaging |
Het |
Ano7 |
G |
A |
1: 93,325,085 (GRCm39) |
V546M |
possibly damaging |
Het |
Aox1 |
G |
A |
1: 58,349,254 (GRCm39) |
|
probably null |
Het |
Asah1 |
G |
T |
8: 41,813,314 (GRCm39) |
S33* |
probably null |
Het |
Astn1 |
C |
T |
1: 158,484,763 (GRCm39) |
S15F |
possibly damaging |
Het |
Bag4 |
A |
T |
8: 26,261,272 (GRCm39) |
Y156* |
probably null |
Het |
Bmpr1b |
T |
C |
3: 141,550,948 (GRCm39) |
E381G |
probably damaging |
Het |
Btnl7-ps |
A |
G |
17: 34,756,092 (GRCm39) |
|
noncoding transcript |
Het |
Caap1 |
A |
T |
4: 94,409,297 (GRCm39) |
|
probably null |
Het |
Card10 |
C |
T |
15: 78,686,580 (GRCm39) |
|
probably null |
Het |
Ccp110 |
T |
C |
7: 118,321,614 (GRCm39) |
V423A |
possibly damaging |
Het |
Cdc123 |
A |
G |
2: 5,809,748 (GRCm39) |
L221P |
possibly damaging |
Het |
Cdh19 |
A |
G |
1: 110,882,354 (GRCm39) |
V46A |
possibly damaging |
Het |
Cfap57 |
A |
G |
4: 118,477,568 (GRCm39) |
F12S |
probably damaging |
Het |
Clvs1 |
A |
G |
4: 9,350,857 (GRCm39) |
|
probably benign |
Het |
Dhx32 |
T |
A |
7: 133,340,384 (GRCm39) |
|
probably benign |
Het |
Dpf3 |
G |
T |
12: 83,417,385 (GRCm39) |
S29* |
probably null |
Het |
Efcab7 |
C |
A |
4: 99,719,780 (GRCm39) |
S87R |
probably damaging |
Het |
Fam81a |
G |
A |
9: 70,000,872 (GRCm39) |
Q291* |
probably null |
Het |
Fbxo41 |
G |
T |
6: 85,454,906 (GRCm39) |
N667K |
probably damaging |
Het |
Flacc1 |
T |
C |
1: 58,698,441 (GRCm39) |
T326A |
probably benign |
Het |
Gm10313 |
A |
T |
8: 46,708,462 (GRCm39) |
|
noncoding transcript |
Het |
Gm28051 |
G |
A |
12: 102,686,430 (GRCm39) |
Q77* |
probably null |
Het |
Gm5535 |
T |
A |
2: 144,016,569 (GRCm39) |
|
noncoding transcript |
Het |
Gtf2ird1 |
A |
T |
5: 134,431,038 (GRCm39) |
D339E |
probably damaging |
Het |
Gvin3 |
A |
T |
7: 106,199,864 (GRCm39) |
|
noncoding transcript |
Het |
Igfbp7 |
A |
G |
5: 77,555,608 (GRCm39) |
M85T |
possibly damaging |
Het |
Il20ra |
A |
G |
10: 19,634,691 (GRCm39) |
T311A |
possibly damaging |
Het |
Il24 |
T |
C |
1: 130,811,179 (GRCm39) |
|
probably null |
Het |
Itch |
T |
C |
2: 155,027,513 (GRCm39) |
F379L |
possibly damaging |
Het |
Itgad |
T |
A |
7: 127,789,015 (GRCm39) |
V488D |
possibly damaging |
Het |
Itpr2 |
A |
T |
6: 146,135,489 (GRCm39) |
M1814K |
possibly damaging |
Het |
Kirrel3 |
A |
G |
9: 34,855,735 (GRCm39) |
E92G |
possibly damaging |
Het |
Lpin2 |
T |
C |
17: 71,538,329 (GRCm39) |
V325A |
probably damaging |
Het |
Lrba |
C |
T |
3: 86,132,678 (GRCm39) |
T28M |
probably benign |
Het |
Lrch3 |
T |
C |
16: 32,818,883 (GRCm39) |
Y661H |
probably damaging |
Het |
Lrfn5 |
C |
A |
12: 61,886,461 (GRCm39) |
S83Y |
probably damaging |
Het |
Lrp1 |
A |
C |
10: 127,375,389 (GRCm39) |
L4435R |
probably benign |
Het |
Lrrn1 |
A |
G |
6: 107,546,305 (GRCm39) |
D701G |
probably benign |
Het |
Map4k3 |
A |
T |
17: 80,961,332 (GRCm39) |
Y125N |
probably benign |
Het |
Mau2 |
A |
T |
8: 70,480,353 (GRCm39) |
H273Q |
possibly damaging |
Het |
Med16 |
A |
C |
10: 79,742,871 (GRCm39) |
|
probably null |
Het |
Mmp17 |
A |
G |
5: 129,679,229 (GRCm39) |
H376R |
possibly damaging |
Het |
Nlrp12 |
G |
A |
7: 3,289,613 (GRCm39) |
H300Y |
possibly damaging |
Het |
Nlrp3 |
A |
T |
11: 59,439,554 (GRCm39) |
Y377F |
probably damaging |
Het |
Notch2 |
T |
C |
3: 98,008,952 (GRCm39) |
|
probably null |
Het |
Nudcd1 |
A |
T |
15: 44,240,039 (GRCm39) |
C500* |
probably null |
Het |
Or52z14 |
T |
C |
7: 103,253,197 (GRCm39) |
I112T |
probably damaging |
Het |
Or5d37 |
A |
G |
2: 87,923,353 (GRCm39) |
V309A |
probably damaging |
Het |
Or6b6 |
T |
A |
7: 106,570,778 (GRCm39) |
M258L |
probably benign |
Het |
Or8g23 |
A |
T |
9: 38,971,827 (GRCm39) |
M45K |
probably benign |
Het |
Or8h9 |
A |
T |
2: 86,789,698 (GRCm39) |
Y35N |
probably damaging |
Het |
Pcdhb20 |
T |
A |
18: 37,639,824 (GRCm39) |
N783K |
probably benign |
Het |
Pclo |
T |
A |
5: 14,727,896 (GRCm39) |
|
probably benign |
Het |
Pdyn |
T |
A |
2: 129,530,021 (GRCm39) |
D216V |
probably damaging |
Het |
Phldb3 |
A |
T |
7: 24,324,110 (GRCm39) |
I495F |
possibly damaging |
Het |
Pmpca |
A |
T |
2: 26,285,178 (GRCm39) |
I468F |
probably damaging |
Het |
Pmpcb |
G |
A |
5: 21,961,441 (GRCm39) |
R399H |
probably damaging |
Het |
Polrmt |
G |
T |
10: 79,572,421 (GRCm39) |
H1145N |
probably damaging |
Het |
Proser1 |
A |
G |
3: 53,371,727 (GRCm39) |
D11G |
probably damaging |
Het |
Ptprc |
A |
G |
1: 138,022,037 (GRCm39) |
S544P |
probably damaging |
Het |
Ptprn2 |
G |
A |
12: 117,240,215 (GRCm39) |
E991K |
probably damaging |
Het |
Pwp2 |
A |
C |
10: 78,009,527 (GRCm39) |
L797R |
possibly damaging |
Het |
Rbm20 |
G |
A |
19: 53,840,100 (GRCm39) |
A1030T |
probably damaging |
Het |
Rdh7 |
T |
C |
10: 127,721,691 (GRCm39) |
Y195C |
probably benign |
Het |
Rev3l |
T |
A |
10: 39,699,326 (GRCm39) |
D1274E |
probably benign |
Het |
Scfd2 |
G |
T |
5: 74,366,982 (GRCm39) |
H639Q |
probably benign |
Het |
Sell |
T |
A |
1: 163,892,887 (GRCm39) |
H34Q |
possibly damaging |
Het |
Senp8 |
A |
C |
9: 59,644,504 (GRCm39) |
D204E |
probably benign |
Het |
Setd2 |
A |
G |
9: 110,377,226 (GRCm39) |
D347G |
probably benign |
Het |
Sh2b1 |
T |
A |
7: 126,067,975 (GRCm39) |
R560W |
probably damaging |
Het |
Slc36a3 |
T |
A |
11: 55,039,399 (GRCm39) |
K76N |
probably damaging |
Het |
Slc6a9 |
A |
T |
4: 117,713,205 (GRCm39) |
Y60F |
probably damaging |
Het |
Slfn10-ps |
C |
T |
11: 82,921,207 (GRCm39) |
|
noncoding transcript |
Het |
Spata31d1d |
G |
A |
13: 59,875,334 (GRCm39) |
H734Y |
probably benign |
Het |
Spmip10 |
G |
T |
18: 56,725,494 (GRCm39) |
M46I |
possibly damaging |
Het |
Spsb1 |
T |
A |
4: 149,991,612 (GRCm39) |
|
probably benign |
Het |
Sptbn5 |
T |
A |
2: 119,882,258 (GRCm39) |
|
noncoding transcript |
Het |
Sugp2 |
G |
A |
8: 70,712,462 (GRCm39) |
V1026I |
possibly damaging |
Het |
Syt14 |
T |
A |
1: 192,613,285 (GRCm39) |
|
probably benign |
Het |
Sytl1 |
G |
A |
4: 132,982,893 (GRCm39) |
Q373* |
probably null |
Het |
Trim38 |
T |
A |
13: 23,975,312 (GRCm39) |
L417Q |
probably damaging |
Het |
Ttll1 |
T |
C |
15: 83,380,597 (GRCm39) |
H256R |
probably damaging |
Het |
Ttyh2 |
A |
T |
11: 114,587,583 (GRCm39) |
T195S |
probably benign |
Het |
Unc119b |
A |
G |
5: 115,263,553 (GRCm39) |
L217P |
probably damaging |
Het |
Usp6nl |
A |
G |
2: 6,425,714 (GRCm39) |
K152E |
probably benign |
Het |
Vcam1 |
T |
C |
3: 115,910,941 (GRCm39) |
R486G |
probably benign |
Het |
Vmn1r225 |
G |
A |
17: 20,722,831 (GRCm39) |
G91S |
possibly damaging |
Het |
Vmn2r1 |
A |
C |
3: 63,997,544 (GRCm39) |
Q400P |
possibly damaging |
Het |
Vmn2r87 |
A |
T |
10: 130,314,422 (GRCm39) |
L388Q |
probably damaging |
Het |
Wnk1 |
A |
T |
6: 119,942,696 (GRCm39) |
|
probably benign |
Het |
Zfp239 |
A |
G |
6: 117,847,478 (GRCm39) |
|
probably benign |
Het |
Zfp688 |
T |
C |
7: 127,018,327 (GRCm39) |
Y266C |
probably damaging |
Het |
Zfp850 |
A |
T |
7: 27,689,658 (GRCm39) |
C183* |
probably null |
Het |
Zscan29 |
T |
C |
2: 120,999,676 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Dgkh |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00654:Dgkh
|
APN |
14 |
78,847,033 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00767:Dgkh
|
APN |
14 |
78,824,701 (GRCm39) |
splice site |
probably benign |
|
IGL00787:Dgkh
|
APN |
14 |
78,855,954 (GRCm39) |
splice site |
probably benign |
|
IGL01503:Dgkh
|
APN |
14 |
78,853,710 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02308:Dgkh
|
APN |
14 |
78,825,016 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02707:Dgkh
|
APN |
14 |
78,823,091 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02987:Dgkh
|
APN |
14 |
78,827,312 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03058:Dgkh
|
APN |
14 |
78,865,237 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03341:Dgkh
|
APN |
14 |
78,832,931 (GRCm39) |
splice site |
probably benign |
|
PIT1430001:Dgkh
|
UTSW |
14 |
78,818,953 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4445001:Dgkh
|
UTSW |
14 |
78,813,382 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0153:Dgkh
|
UTSW |
14 |
78,807,569 (GRCm39) |
nonsense |
probably null |
|
R0730:Dgkh
|
UTSW |
14 |
78,821,919 (GRCm39) |
missense |
probably damaging |
0.99 |
R1136:Dgkh
|
UTSW |
14 |
78,862,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R1162:Dgkh
|
UTSW |
14 |
78,861,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R1689:Dgkh
|
UTSW |
14 |
78,855,984 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1771:Dgkh
|
UTSW |
14 |
78,846,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R1861:Dgkh
|
UTSW |
14 |
78,816,232 (GRCm39) |
missense |
probably benign |
0.04 |
R1916:Dgkh
|
UTSW |
14 |
78,832,663 (GRCm39) |
missense |
probably damaging |
0.97 |
R1930:Dgkh
|
UTSW |
14 |
78,853,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R1931:Dgkh
|
UTSW |
14 |
78,853,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R1956:Dgkh
|
UTSW |
14 |
78,855,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R2007:Dgkh
|
UTSW |
14 |
78,840,489 (GRCm39) |
missense |
probably benign |
0.09 |
R3747:Dgkh
|
UTSW |
14 |
78,821,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R4446:Dgkh
|
UTSW |
14 |
78,865,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R4475:Dgkh
|
UTSW |
14 |
78,827,318 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4965:Dgkh
|
UTSW |
14 |
78,861,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R5071:Dgkh
|
UTSW |
14 |
78,841,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Dgkh
|
UTSW |
14 |
78,865,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Dgkh
|
UTSW |
14 |
78,862,342 (GRCm39) |
missense |
probably benign |
0.16 |
R5773:Dgkh
|
UTSW |
14 |
78,832,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R5855:Dgkh
|
UTSW |
14 |
78,861,944 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6041:Dgkh
|
UTSW |
14 |
78,825,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Dgkh
|
UTSW |
14 |
78,865,504 (GRCm39) |
nonsense |
probably null |
|
R6868:Dgkh
|
UTSW |
14 |
78,862,293 (GRCm39) |
missense |
probably damaging |
0.99 |
R6981:Dgkh
|
UTSW |
14 |
78,865,182 (GRCm39) |
nonsense |
probably null |
|
R7095:Dgkh
|
UTSW |
14 |
78,865,224 (GRCm39) |
missense |
probably benign |
0.07 |
R7473:Dgkh
|
UTSW |
14 |
78,836,483 (GRCm39) |
missense |
probably benign |
0.00 |
R7495:Dgkh
|
UTSW |
14 |
78,816,239 (GRCm39) |
missense |
probably benign |
|
R7711:Dgkh
|
UTSW |
14 |
78,962,459 (GRCm39) |
missense |
probably benign |
|
R7727:Dgkh
|
UTSW |
14 |
78,832,585 (GRCm39) |
critical splice donor site |
probably null |
|
R7823:Dgkh
|
UTSW |
14 |
78,841,921 (GRCm39) |
missense |
probably benign |
|
R7846:Dgkh
|
UTSW |
14 |
78,856,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R7967:Dgkh
|
UTSW |
14 |
78,857,256 (GRCm39) |
missense |
probably benign |
0.10 |
R8085:Dgkh
|
UTSW |
14 |
78,824,558 (GRCm39) |
critical splice donor site |
probably null |
|
R8285:Dgkh
|
UTSW |
14 |
78,865,566 (GRCm39) |
missense |
probably benign |
0.18 |
R8669:Dgkh
|
UTSW |
14 |
78,962,459 (GRCm39) |
missense |
probably benign |
|
R9069:Dgkh
|
UTSW |
14 |
78,853,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R9187:Dgkh
|
UTSW |
14 |
78,832,601 (GRCm39) |
missense |
probably damaging |
0.97 |
R9225:Dgkh
|
UTSW |
14 |
78,962,507 (GRCm39) |
missense |
probably damaging |
0.98 |
R9410:Dgkh
|
UTSW |
14 |
78,862,293 (GRCm39) |
missense |
probably damaging |
0.99 |
R9615:Dgkh
|
UTSW |
14 |
78,813,370 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9761:Dgkh
|
UTSW |
14 |
78,889,163 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Dgkh
|
UTSW |
14 |
78,832,901 (GRCm39) |
missense |
probably damaging |
1.00 |
|