Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
A |
T |
8: 87,293,168 (GRCm39) |
Y7N |
probably damaging |
Het |
Adcy1 |
A |
C |
11: 7,111,351 (GRCm39) |
I881L |
probably benign |
Het |
Aftph |
T |
C |
11: 20,676,994 (GRCm39) |
D205G |
probably damaging |
Het |
Aldh7a1 |
T |
A |
18: 56,667,325 (GRCm39) |
N316Y |
possibly damaging |
Het |
Ankrd36 |
A |
G |
11: 5,639,340 (GRCm39) |
|
probably benign |
Het |
Ccdc88a |
T |
G |
11: 29,448,416 (GRCm39) |
N1465K |
possibly damaging |
Het |
Ccpg1 |
G |
A |
9: 72,920,326 (GRCm39) |
S647N |
probably benign |
Het |
Cep70 |
T |
A |
9: 99,163,128 (GRCm39) |
L325Q |
probably damaging |
Het |
Cfap46 |
A |
G |
7: 139,193,423 (GRCm39) |
|
probably null |
Het |
Cftr |
C |
T |
6: 18,226,128 (GRCm39) |
Q359* |
probably null |
Het |
Chrne |
A |
T |
11: 70,505,913 (GRCm39) |
N457K |
possibly damaging |
Het |
Cntn2 |
A |
G |
1: 132,451,415 (GRCm39) |
I438T |
probably benign |
Het |
Cntn4 |
T |
C |
6: 106,158,765 (GRCm39) |
L10P |
possibly damaging |
Het |
Copg1 |
G |
T |
6: 87,867,189 (GRCm39) |
M87I |
possibly damaging |
Het |
Cyfip1 |
A |
T |
7: 55,574,883 (GRCm39) |
M1045L |
possibly damaging |
Het |
Cyp2c29 |
C |
T |
19: 39,318,816 (GRCm39) |
P432L |
probably damaging |
Het |
Dcaf11 |
T |
A |
14: 55,800,833 (GRCm39) |
D96E |
probably damaging |
Het |
Dmxl2 |
A |
G |
9: 54,286,041 (GRCm39) |
S2715P |
probably benign |
Het |
Dnhd1 |
G |
A |
7: 105,363,644 (GRCm39) |
E4069K |
possibly damaging |
Het |
Duox2 |
A |
G |
2: 122,125,617 (GRCm39) |
V330A |
probably benign |
Het |
Dusp11 |
T |
C |
6: 85,924,587 (GRCm39) |
*322W |
probably null |
Het |
Dusp8 |
T |
A |
7: 141,643,730 (GRCm39) |
Q61L |
possibly damaging |
Het |
Eml3 |
G |
A |
19: 8,916,638 (GRCm39) |
G720S |
probably damaging |
Het |
F11 |
A |
G |
8: 45,699,833 (GRCm39) |
S418P |
probably damaging |
Het |
Fam91a1 |
G |
A |
15: 58,320,243 (GRCm39) |
S645N |
probably benign |
Het |
Fat2 |
G |
A |
11: 55,158,482 (GRCm39) |
T3412I |
probably benign |
Het |
Fbxo38 |
A |
G |
18: 62,674,042 (GRCm39) |
M13T |
probably benign |
Het |
Fbxo48 |
G |
T |
11: 16,904,329 (GRCm39) |
L160F |
possibly damaging |
Het |
Gm10134 |
T |
A |
2: 28,396,372 (GRCm39) |
|
probably benign |
Het |
Gm11787 |
T |
C |
4: 3,511,795 (GRCm39) |
|
noncoding transcript |
Het |
Gpatch8 |
A |
T |
11: 102,399,053 (GRCm39) |
|
probably null |
Het |
Gucy2g |
G |
A |
19: 55,203,548 (GRCm39) |
A750V |
probably damaging |
Het |
Hephl1 |
T |
C |
9: 14,988,150 (GRCm39) |
T653A |
possibly damaging |
Het |
Herc3 |
T |
A |
6: 58,851,263 (GRCm39) |
M504K |
probably damaging |
Het |
Hmcn2 |
A |
G |
2: 31,350,333 (GRCm39) |
T5077A |
probably benign |
Het |
Ifitm3 |
T |
C |
7: 140,590,554 (GRCm39) |
N2S |
probably benign |
Het |
Ighe |
T |
C |
12: 113,235,092 (GRCm39) |
H356R |
probably benign |
Het |
Ighv10-3 |
T |
A |
12: 114,487,125 (GRCm39) |
M99L |
probably benign |
Het |
Izumo4 |
C |
A |
10: 80,538,639 (GRCm39) |
C30* |
probably null |
Het |
Jag1 |
A |
T |
2: 136,937,464 (GRCm39) |
H303Q |
possibly damaging |
Het |
Kif24 |
T |
C |
4: 41,395,373 (GRCm39) |
E500G |
probably benign |
Het |
Kng1 |
A |
T |
16: 22,897,842 (GRCm39) |
D414V |
probably damaging |
Het |
Loxhd1 |
A |
C |
18: 77,451,308 (GRCm39) |
D410A |
probably damaging |
Het |
Ltn1 |
T |
C |
16: 87,212,899 (GRCm39) |
K554R |
possibly damaging |
Het |
Ly75 |
A |
G |
2: 60,133,985 (GRCm39) |
C1547R |
probably damaging |
Het |
Ms4a6d |
A |
T |
19: 11,564,500 (GRCm39) |
S124T |
possibly damaging |
Het |
Mtcl3 |
A |
G |
10: 29,072,766 (GRCm39) |
D686G |
probably benign |
Het |
Mtfr2 |
A |
G |
10: 20,233,448 (GRCm39) |
D339G |
probably damaging |
Het |
Myh10 |
T |
A |
11: 68,692,434 (GRCm39) |
L1369Q |
probably damaging |
Het |
Myh11 |
A |
T |
16: 14,025,872 (GRCm39) |
V1366D |
possibly damaging |
Het |
Nadsyn1 |
A |
G |
7: 143,357,023 (GRCm39) |
V491A |
possibly damaging |
Het |
Nav3 |
T |
C |
10: 109,688,966 (GRCm39) |
N437S |
probably benign |
Het |
Ncf1 |
A |
G |
5: 134,250,659 (GRCm39) |
L373P |
probably damaging |
Het |
Neb |
A |
T |
2: 52,079,873 (GRCm39) |
I85N |
probably damaging |
Het |
Nktr |
A |
G |
9: 121,577,659 (GRCm39) |
K576E |
probably benign |
Het |
Nmur2 |
T |
A |
11: 55,931,040 (GRCm39) |
I224F |
probably damaging |
Het |
Oas3 |
A |
G |
5: 120,895,055 (GRCm39) |
F978S |
probably damaging |
Het |
Or10ag53 |
C |
T |
2: 87,082,827 (GRCm39) |
P182L |
probably benign |
Het |
Or10ak9 |
T |
C |
4: 118,726,772 (GRCm39) |
S264P |
probably damaging |
Het |
Or2r3 |
T |
A |
6: 42,448,186 (GRCm39) |
I309F |
probably benign |
Het |
Or2t48 |
A |
T |
11: 58,420,308 (GRCm39) |
M168K |
probably damaging |
Het |
Or5p60 |
T |
C |
7: 107,724,375 (GRCm39) |
T32A |
probably benign |
Het |
Pcyox1 |
A |
T |
6: 86,369,336 (GRCm39) |
|
probably null |
Het |
Pdcd7 |
G |
A |
9: 65,265,974 (GRCm39) |
W477* |
probably null |
Het |
Pitpnm1 |
T |
C |
19: 4,153,435 (GRCm39) |
F197S |
probably damaging |
Het |
Plce1 |
C |
A |
19: 38,748,535 (GRCm39) |
N1755K |
probably damaging |
Het |
Pnpla7 |
C |
A |
2: 24,931,031 (GRCm39) |
P882Q |
probably damaging |
Het |
Pold2 |
A |
G |
11: 5,826,760 (GRCm39) |
L58P |
probably damaging |
Het |
Pomt1 |
C |
G |
2: 32,134,311 (GRCm39) |
Y277* |
probably null |
Het |
Pou4f2 |
A |
G |
8: 79,162,958 (GRCm39) |
Y26H |
unknown |
Het |
Pphln1-ps1 |
T |
G |
16: 13,495,622 (GRCm39) |
N240K |
probably benign |
Het |
Ppm1e |
A |
T |
11: 87,249,377 (GRCm39) |
L118Q |
possibly damaging |
Het |
Pramel34 |
C |
T |
5: 93,785,607 (GRCm39) |
M224I |
possibly damaging |
Het |
Prdx2 |
T |
A |
8: 85,698,302 (GRCm39) |
Y164* |
probably null |
Het |
Prkra |
T |
G |
2: 76,469,622 (GRCm39) |
T146P |
probably damaging |
Het |
Prpf8 |
A |
G |
11: 75,386,625 (GRCm39) |
D1038G |
probably damaging |
Het |
Rab4a |
A |
T |
8: 124,554,113 (GRCm39) |
I16L |
probably benign |
Het |
Rai2 |
A |
G |
X: 160,561,636 (GRCm39) |
N363S |
probably benign |
Het |
Ranbp17 |
A |
T |
11: 33,169,241 (GRCm39) |
V991D |
possibly damaging |
Het |
Rimbp2 |
G |
A |
5: 128,865,656 (GRCm39) |
T557M |
probably benign |
Het |
Rmi1 |
G |
A |
13: 58,557,280 (GRCm39) |
G510R |
probably damaging |
Het |
Sdad1 |
A |
G |
5: 92,434,684 (GRCm39) |
*687Q |
probably null |
Het |
Sema6d |
T |
C |
2: 124,506,166 (GRCm39) |
L720P |
probably damaging |
Het |
Setx |
T |
G |
2: 29,024,045 (GRCm39) |
|
probably null |
Het |
Sgsm3 |
T |
C |
15: 80,892,200 (GRCm39) |
V256A |
probably benign |
Het |
Slc28a2b |
C |
A |
2: 122,353,259 (GRCm39) |
L480I |
probably benign |
Het |
Sppl2c |
T |
A |
11: 104,078,127 (GRCm39) |
I309K |
possibly damaging |
Het |
Stard9 |
A |
G |
2: 120,531,111 (GRCm39) |
E2456G |
probably damaging |
Het |
Strn3 |
C |
G |
12: 51,694,803 (GRCm39) |
R320P |
probably damaging |
Het |
Supv3l1 |
A |
T |
10: 62,266,375 (GRCm39) |
N600K |
possibly damaging |
Het |
Syne2 |
T |
A |
12: 76,146,112 (GRCm39) |
S6377T |
possibly damaging |
Het |
Tas2r123 |
A |
T |
6: 132,824,190 (GRCm39) |
H29L |
probably benign |
Het |
Tbl3 |
C |
T |
17: 24,924,944 (GRCm39) |
V52M |
possibly damaging |
Het |
Tbp |
A |
G |
17: 15,727,609 (GRCm39) |
I145V |
probably benign |
Het |
Tcf20 |
A |
T |
15: 82,739,910 (GRCm39) |
S514T |
possibly damaging |
Het |
Tgm4 |
A |
G |
9: 122,885,559 (GRCm39) |
Y367C |
probably damaging |
Het |
Tle1 |
C |
T |
4: 72,060,081 (GRCm39) |
V258M |
probably damaging |
Het |
Tln1 |
C |
T |
4: 43,540,661 (GRCm39) |
V1447I |
probably benign |
Het |
Tnfrsf11b |
C |
T |
15: 54,141,622 (GRCm39) |
A8T |
probably benign |
Het |
Trim80 |
A |
T |
11: 115,338,843 (GRCm39) |
T558S |
probably benign |
Het |
Trmt6 |
C |
A |
2: 132,650,703 (GRCm39) |
A302S |
probably benign |
Het |
Tsen15 |
C |
T |
1: 152,259,131 (GRCm39) |
V76I |
probably damaging |
Het |
Ttc17 |
A |
T |
2: 94,133,985 (GRCm39) |
W1067R |
probably damaging |
Het |
Ucn3 |
A |
T |
13: 3,991,474 (GRCm39) |
F59L |
probably benign |
Het |
Ulk3 |
T |
A |
9: 57,498,023 (GRCm39) |
I108N |
possibly damaging |
Het |
Vmn2r94 |
A |
C |
17: 18,464,728 (GRCm39) |
Y521D |
probably damaging |
Het |
Vps45 |
T |
C |
3: 95,965,086 (GRCm39) |
M1V |
probably null |
Het |
Vta1 |
C |
A |
10: 14,581,143 (GRCm39) |
L21F |
probably damaging |
Het |
Zdhhc21 |
C |
T |
4: 82,765,929 (GRCm39) |
G2D |
probably damaging |
Het |
Zfp169 |
A |
T |
13: 48,643,751 (GRCm39) |
C459S |
possibly damaging |
Het |
Zfp90 |
C |
T |
8: 107,152,000 (GRCm39) |
T571M |
probably damaging |
Het |
Zswim8 |
A |
T |
14: 20,768,939 (GRCm39) |
N1119I |
possibly damaging |
Het |
|
Other mutations in Dpy19l4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00479:Dpy19l4
|
APN |
4 |
11,290,411 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01402:Dpy19l4
|
APN |
4 |
11,273,006 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01404:Dpy19l4
|
APN |
4 |
11,273,006 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01643:Dpy19l4
|
APN |
4 |
11,290,184 (GRCm39) |
splice site |
probably benign |
|
IGL01758:Dpy19l4
|
APN |
4 |
11,265,846 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01896:Dpy19l4
|
APN |
4 |
11,267,752 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02222:Dpy19l4
|
APN |
4 |
11,281,116 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02314:Dpy19l4
|
APN |
4 |
11,267,720 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02422:Dpy19l4
|
APN |
4 |
11,265,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02565:Dpy19l4
|
APN |
4 |
11,309,440 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03121:Dpy19l4
|
APN |
4 |
11,303,334 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03357:Dpy19l4
|
APN |
4 |
11,267,615 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03368:Dpy19l4
|
APN |
4 |
11,290,253 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0003:Dpy19l4
|
UTSW |
4 |
11,267,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R0481:Dpy19l4
|
UTSW |
4 |
11,272,993 (GRCm39) |
splice site |
probably benign |
|
R0506:Dpy19l4
|
UTSW |
4 |
11,289,715 (GRCm39) |
missense |
probably benign |
0.07 |
R1114:Dpy19l4
|
UTSW |
4 |
11,287,643 (GRCm39) |
splice site |
probably benign |
|
R1332:Dpy19l4
|
UTSW |
4 |
11,276,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R1336:Dpy19l4
|
UTSW |
4 |
11,276,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R1355:Dpy19l4
|
UTSW |
4 |
11,303,371 (GRCm39) |
nonsense |
probably null |
|
R1421:Dpy19l4
|
UTSW |
4 |
11,304,011 (GRCm39) |
missense |
probably benign |
0.09 |
R1422:Dpy19l4
|
UTSW |
4 |
11,317,168 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1465:Dpy19l4
|
UTSW |
4 |
11,296,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Dpy19l4
|
UTSW |
4 |
11,296,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R1766:Dpy19l4
|
UTSW |
4 |
11,303,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R1803:Dpy19l4
|
UTSW |
4 |
11,281,020 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2090:Dpy19l4
|
UTSW |
4 |
11,304,344 (GRCm39) |
missense |
probably benign |
0.34 |
R2324:Dpy19l4
|
UTSW |
4 |
11,276,857 (GRCm39) |
unclassified |
probably benign |
|
R2446:Dpy19l4
|
UTSW |
4 |
11,304,143 (GRCm39) |
splice site |
probably null |
|
R3769:Dpy19l4
|
UTSW |
4 |
11,276,868 (GRCm39) |
splice site |
probably null |
|
R4151:Dpy19l4
|
UTSW |
4 |
11,309,485 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4472:Dpy19l4
|
UTSW |
4 |
11,304,053 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4609:Dpy19l4
|
UTSW |
4 |
11,295,999 (GRCm39) |
nonsense |
probably null |
|
R4708:Dpy19l4
|
UTSW |
4 |
11,277,970 (GRCm39) |
missense |
probably benign |
0.00 |
R4722:Dpy19l4
|
UTSW |
4 |
11,290,521 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4997:Dpy19l4
|
UTSW |
4 |
11,287,493 (GRCm39) |
missense |
probably benign |
0.01 |
R5085:Dpy19l4
|
UTSW |
4 |
11,265,943 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5088:Dpy19l4
|
UTSW |
4 |
11,303,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R5288:Dpy19l4
|
UTSW |
4 |
11,304,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R5413:Dpy19l4
|
UTSW |
4 |
11,289,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R5758:Dpy19l4
|
UTSW |
4 |
11,276,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R6024:Dpy19l4
|
UTSW |
4 |
11,276,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R6312:Dpy19l4
|
UTSW |
4 |
11,289,671 (GRCm39) |
nonsense |
probably null |
|
R6339:Dpy19l4
|
UTSW |
4 |
11,285,111 (GRCm39) |
missense |
probably damaging |
0.98 |
R7055:Dpy19l4
|
UTSW |
4 |
11,290,291 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7359:Dpy19l4
|
UTSW |
4 |
11,273,125 (GRCm39) |
missense |
probably benign |
0.00 |
R7525:Dpy19l4
|
UTSW |
4 |
11,317,160 (GRCm39) |
nonsense |
probably null |
|
R7579:Dpy19l4
|
UTSW |
4 |
11,265,909 (GRCm39) |
missense |
probably benign |
0.39 |
R7913:Dpy19l4
|
UTSW |
4 |
11,265,859 (GRCm39) |
nonsense |
probably null |
|
R8047:Dpy19l4
|
UTSW |
4 |
11,317,139 (GRCm39) |
missense |
probably benign |
0.00 |
R8049:Dpy19l4
|
UTSW |
4 |
11,303,982 (GRCm39) |
missense |
probably benign |
0.44 |
R8495:Dpy19l4
|
UTSW |
4 |
11,267,659 (GRCm39) |
missense |
probably benign |
|
R8911:Dpy19l4
|
UTSW |
4 |
11,317,078 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8928:Dpy19l4
|
UTSW |
4 |
11,304,674 (GRCm39) |
intron |
probably benign |
|
R8955:Dpy19l4
|
UTSW |
4 |
11,290,195 (GRCm39) |
missense |
probably benign |
0.00 |
R9332:Dpy19l4
|
UTSW |
4 |
11,304,298 (GRCm39) |
critical splice donor site |
probably null |
|
R9372:Dpy19l4
|
UTSW |
4 |
11,303,343 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9401:Dpy19l4
|
UTSW |
4 |
11,265,806 (GRCm39) |
missense |
probably benign |
0.29 |
|