Other mutations in this stock |
Total: 111 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
C |
T |
13: 77,418,039 (GRCm39) |
T741I |
possibly damaging |
Het |
Aadacl4fm2 |
A |
T |
4: 144,281,976 (GRCm39) |
I272K |
probably damaging |
Het |
Acot3 |
A |
T |
12: 84,100,347 (GRCm39) |
Q41L |
probably damaging |
Het |
Actl7b |
G |
A |
4: 56,740,165 (GRCm39) |
Q398* |
probably null |
Het |
Adgrb2 |
C |
A |
4: 129,886,417 (GRCm39) |
Q186K |
probably damaging |
Het |
Akr1a1 |
A |
G |
4: 116,495,171 (GRCm39) |
|
probably null |
Het |
Ap3s2 |
A |
T |
7: 79,530,238 (GRCm39) |
F192L |
probably damaging |
Het |
Apobr |
T |
G |
7: 126,184,151 (GRCm39) |
|
probably null |
Het |
Arhgap5 |
A |
G |
12: 52,566,128 (GRCm39) |
N1033S |
probably damaging |
Het |
Arid3c |
G |
T |
4: 41,725,947 (GRCm39) |
R219S |
probably damaging |
Het |
Bves |
C |
T |
10: 45,223,961 (GRCm39) |
T207M |
probably damaging |
Het |
Cacna1d |
T |
C |
14: 29,788,013 (GRCm39) |
K1619R |
probably damaging |
Het |
Caps2 |
A |
T |
10: 112,026,883 (GRCm39) |
D223V |
possibly damaging |
Het |
Cd3g |
A |
C |
9: 44,885,640 (GRCm39) |
L35R |
probably damaging |
Het |
Cdh23 |
A |
T |
10: 60,359,315 (GRCm39) |
V261E |
probably benign |
Het |
Cfap54 |
T |
G |
10: 92,846,882 (GRCm39) |
T1028P |
probably damaging |
Het |
Ch25h |
C |
A |
19: 34,451,686 (GRCm39) |
V281L |
probably benign |
Het |
Cip2a |
A |
C |
16: 48,837,849 (GRCm39) |
I850L |
probably benign |
Het |
Clu |
G |
T |
14: 66,218,354 (GRCm39) |
V405L |
possibly damaging |
Het |
Col6a3 |
A |
T |
1: 90,757,935 (GRCm39) |
H6Q |
probably damaging |
Het |
Cps1 |
G |
A |
1: 67,207,533 (GRCm39) |
|
probably null |
Het |
Ctr9 |
T |
C |
7: 110,654,870 (GRCm39) |
S1134P |
unknown |
Het |
Cts7 |
C |
T |
13: 61,500,624 (GRCm39) |
G308S |
probably damaging |
Het |
Cyp2c39 |
C |
A |
19: 39,555,335 (GRCm39) |
T385K |
probably damaging |
Het |
Dennd5a |
A |
T |
7: 109,517,919 (GRCm39) |
D596E |
probably benign |
Het |
Disc1 |
T |
A |
8: 125,851,349 (GRCm39) |
I413K |
probably benign |
Het |
Dnah3 |
A |
G |
7: 119,677,794 (GRCm39) |
W377R |
probably damaging |
Het |
Dop1b |
A |
G |
16: 93,596,814 (GRCm39) |
D1792G |
probably damaging |
Het |
Dpep3 |
T |
A |
8: 106,700,325 (GRCm39) |
R460S |
probably benign |
Het |
Ebf4 |
A |
G |
2: 130,200,751 (GRCm39) |
N302S |
probably damaging |
Het |
Efcab3 |
A |
G |
11: 104,611,514 (GRCm39) |
K452R |
probably benign |
Het |
Egflam |
T |
C |
15: 7,319,396 (GRCm39) |
E194G |
possibly damaging |
Het |
Ep400 |
A |
T |
5: 110,841,174 (GRCm39) |
|
probably benign |
Het |
Ercc6 |
T |
C |
14: 32,248,133 (GRCm39) |
M228T |
probably damaging |
Het |
Fbxo9 |
T |
C |
9: 77,994,529 (GRCm39) |
T264A |
probably damaging |
Het |
Fcrl5 |
C |
A |
3: 87,364,721 (GRCm39) |
P486T |
possibly damaging |
Het |
Fyb1 |
T |
C |
15: 6,609,960 (GRCm39) |
F178L |
probably damaging |
Het |
Gaa |
T |
A |
11: 119,171,286 (GRCm39) |
I646N |
probably damaging |
Het |
Gm5431 |
A |
T |
11: 48,785,853 (GRCm39) |
V174E |
possibly damaging |
Het |
Gnpat |
T |
G |
8: 125,613,691 (GRCm39) |
|
probably null |
Het |
Gucy1a2 |
G |
T |
9: 3,759,622 (GRCm39) |
R476I |
probably benign |
Het |
Hars1 |
A |
G |
18: 36,904,156 (GRCm39) |
L241P |
probably damaging |
Het |
Haus5 |
G |
A |
7: 30,357,328 (GRCm39) |
Q399* |
probably null |
Het |
Hephl1 |
T |
C |
9: 14,970,542 (GRCm39) |
E984G |
probably damaging |
Het |
Hmces |
C |
T |
6: 87,898,574 (GRCm39) |
Q132* |
probably null |
Het |
Hsp90b1 |
G |
T |
10: 86,530,389 (GRCm39) |
T490K |
probably damaging |
Het |
Idh2 |
T |
G |
7: 79,748,906 (GRCm39) |
E125A |
probably damaging |
Het |
Ipo13 |
G |
T |
4: 117,761,719 (GRCm39) |
H465Q |
probably benign |
Het |
Isca2 |
C |
A |
12: 84,820,393 (GRCm39) |
T31K |
probably damaging |
Het |
Itga9 |
T |
C |
9: 118,527,529 (GRCm39) |
V560A |
probably benign |
Het |
Jhy |
G |
A |
9: 40,822,453 (GRCm39) |
Q562* |
probably null |
Het |
Kcnj5 |
A |
G |
9: 32,233,865 (GRCm39) |
I150T |
probably damaging |
Het |
Kmt2a |
A |
G |
9: 44,752,918 (GRCm39) |
I1419T |
unknown |
Het |
Lix1 |
T |
C |
17: 17,666,320 (GRCm39) |
F160L |
possibly damaging |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Map4k1 |
A |
T |
7: 28,688,777 (GRCm39) |
Q276L |
possibly damaging |
Het |
Mmp9 |
G |
A |
2: 164,791,342 (GRCm39) |
G171S |
probably damaging |
Het |
Mvp |
C |
A |
7: 126,594,907 (GRCm39) |
|
probably null |
Het |
Mylk3 |
T |
A |
8: 86,091,460 (GRCm39) |
E115V |
probably damaging |
Het |
Nebl |
T |
A |
2: 17,393,565 (GRCm39) |
T603S |
probably damaging |
Het |
Nudt15 |
T |
C |
14: 73,760,776 (GRCm39) |
D105G |
probably benign |
Het |
Or12j2 |
A |
C |
7: 139,915,912 (GRCm39) |
T46P |
possibly damaging |
Het |
Or2w1b |
G |
A |
13: 21,300,476 (GRCm39) |
V205I |
probably benign |
Het |
Or51b6 |
T |
A |
7: 103,555,906 (GRCm39) |
W87R |
probably damaging |
Het |
Or52i2 |
G |
T |
7: 102,319,369 (GRCm39) |
V81L |
probably damaging |
Het |
Or52l1 |
A |
T |
7: 104,829,967 (GRCm39) |
H199Q |
probably damaging |
Het |
Or8g2b |
A |
G |
9: 39,751,581 (GRCm39) |
M284V |
probably benign |
Het |
Osbpl9 |
A |
T |
4: 108,923,415 (GRCm39) |
C495S |
probably damaging |
Het |
Pamr1 |
A |
G |
2: 102,471,197 (GRCm39) |
T507A |
probably benign |
Het |
Pcdhb9 |
T |
A |
18: 37,536,380 (GRCm39) |
C791* |
probably null |
Het |
Pcgf6 |
T |
C |
19: 47,038,957 (GRCm39) |
E101G |
probably damaging |
Het |
Pdgfrl |
A |
T |
8: 41,438,831 (GRCm39) |
I256F |
probably benign |
Het |
Pdzd7 |
T |
C |
19: 45,033,950 (GRCm39) |
R45G |
possibly damaging |
Het |
Pecr |
C |
T |
1: 72,316,568 (GRCm39) |
V46I |
possibly damaging |
Het |
Pgr |
A |
G |
9: 8,922,715 (GRCm39) |
|
probably null |
Het |
Pik3c2a |
A |
T |
7: 116,017,162 (GRCm39) |
Y198* |
probably null |
Het |
Pp2d1 |
T |
A |
17: 53,822,338 (GRCm39) |
M243L |
possibly damaging |
Het |
Ppp1r1a |
T |
A |
15: 103,441,919 (GRCm39) |
I50L |
possibly damaging |
Het |
Proc |
T |
C |
18: 32,260,459 (GRCm39) |
D222G |
probably benign |
Het |
Ptprq |
T |
A |
10: 107,370,560 (GRCm39) |
R2044* |
probably null |
Het |
Ranbp2 |
T |
C |
10: 58,296,341 (GRCm39) |
V326A |
probably benign |
Het |
Reep6 |
T |
A |
10: 80,169,815 (GRCm39) |
F122I |
possibly damaging |
Het |
Rubcn |
C |
A |
16: 32,663,471 (GRCm39) |
R388S |
probably damaging |
Het |
Rusc1 |
A |
G |
3: 88,996,600 (GRCm39) |
L62P |
probably damaging |
Het |
Satb2 |
T |
C |
1: 56,889,448 (GRCm39) |
N423S |
probably damaging |
Het |
Scart1 |
G |
T |
7: 139,800,522 (GRCm39) |
C101F |
probably damaging |
Het |
Serpinb9d |
A |
G |
13: 33,384,731 (GRCm39) |
K236R |
probably benign |
Het |
Slc4a7 |
A |
G |
14: 14,765,709 (GRCm38) |
R680G |
probably benign |
Het |
Slitrk1 |
T |
A |
14: 109,150,528 (GRCm39) |
Y61F |
probably benign |
Het |
Son |
A |
G |
16: 91,457,114 (GRCm39) |
|
probably benign |
Het |
Sparc |
T |
A |
11: 55,286,602 (GRCm39) |
|
probably null |
Het |
Spon2 |
A |
G |
5: 33,373,729 (GRCm39) |
F194S |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,068,608 (GRCm39) |
E2136G |
probably damaging |
Het |
Stat4 |
T |
C |
1: 52,146,084 (GRCm39) |
S746P |
probably damaging |
Het |
Stk31 |
T |
A |
6: 49,446,238 (GRCm39) |
S958R |
probably benign |
Het |
Stom |
T |
A |
2: 35,205,929 (GRCm39) |
I267F |
probably damaging |
Het |
Stx12 |
A |
T |
4: 132,585,788 (GRCm39) |
D197E |
probably damaging |
Het |
Taok3 |
A |
T |
5: 117,393,991 (GRCm39) |
N588I |
possibly damaging |
Het |
Tgs1 |
A |
G |
4: 3,598,658 (GRCm39) |
D657G |
probably damaging |
Het |
Trim6 |
A |
G |
7: 103,882,044 (GRCm39) |
T432A |
probably damaging |
Het |
Trim72 |
C |
G |
7: 127,603,757 (GRCm39) |
C34W |
probably damaging |
Het |
Trpc4ap |
A |
T |
2: 155,499,664 (GRCm39) |
I286N |
probably benign |
Het |
Ttn |
A |
G |
2: 76,693,905 (GRCm39) |
V321A |
possibly damaging |
Het |
Utp4 |
T |
A |
8: 107,645,352 (GRCm39) |
I583N |
probably damaging |
Het |
Wdfy2 |
G |
T |
14: 63,181,546 (GRCm39) |
M225I |
probably benign |
Het |
Wfdc1 |
A |
G |
8: 120,407,776 (GRCm39) |
T134A |
probably benign |
Het |
Wnt9b |
A |
G |
11: 103,622,954 (GRCm39) |
S150P |
probably damaging |
Het |
Zbtb46 |
A |
T |
2: 181,053,477 (GRCm39) |
F412I |
probably damaging |
Het |
Zc3h15 |
G |
A |
2: 83,491,492 (GRCm39) |
R240H |
probably benign |
Het |
Zfp11 |
A |
T |
5: 129,733,737 (GRCm39) |
Y575N |
probably benign |
Het |
Zfp687 |
T |
C |
3: 94,919,200 (GRCm39) |
M191V |
probably benign |
Het |
|
Other mutations in Dll3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0024:Dll3
|
UTSW |
7 |
27,999,586 (GRCm39) |
splice site |
probably benign |
|
R0138:Dll3
|
UTSW |
7 |
28,000,746 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0322:Dll3
|
UTSW |
7 |
27,995,793 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0479:Dll3
|
UTSW |
7 |
28,000,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R1742:Dll3
|
UTSW |
7 |
27,993,848 (GRCm39) |
missense |
probably benign |
0.37 |
R1854:Dll3
|
UTSW |
7 |
27,995,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R1920:Dll3
|
UTSW |
7 |
27,998,348 (GRCm39) |
missense |
probably benign |
|
R3037:Dll3
|
UTSW |
7 |
27,998,542 (GRCm39) |
missense |
probably damaging |
0.99 |
R3158:Dll3
|
UTSW |
7 |
27,993,520 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4306:Dll3
|
UTSW |
7 |
28,001,082 (GRCm39) |
splice site |
probably null |
|
R4424:Dll3
|
UTSW |
7 |
27,995,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R4873:Dll3
|
UTSW |
7 |
27,995,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R4875:Dll3
|
UTSW |
7 |
27,995,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R5604:Dll3
|
UTSW |
7 |
27,994,057 (GRCm39) |
missense |
probably benign |
|
R5770:Dll3
|
UTSW |
7 |
27,998,434 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5988:Dll3
|
UTSW |
7 |
27,993,537 (GRCm39) |
missense |
probably damaging |
0.98 |
R7204:Dll3
|
UTSW |
7 |
27,998,330 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7347:Dll3
|
UTSW |
7 |
27,998,536 (GRCm39) |
missense |
probably damaging |
0.99 |
R7373:Dll3
|
UTSW |
7 |
27,994,057 (GRCm39) |
missense |
probably benign |
|
R7694:Dll3
|
UTSW |
7 |
28,001,170 (GRCm39) |
start codon destroyed |
probably null |
0.83 |
R7829:Dll3
|
UTSW |
7 |
27,994,075 (GRCm39) |
missense |
probably damaging |
0.99 |
R7905:Dll3
|
UTSW |
7 |
28,000,960 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8681:Dll3
|
UTSW |
7 |
27,994,270 (GRCm39) |
missense |
probably damaging |
0.99 |
R8988:Dll3
|
UTSW |
7 |
27,995,793 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9519:Dll3
|
UTSW |
7 |
27,995,764 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Dll3
|
UTSW |
7 |
28,000,808 (GRCm39) |
missense |
probably damaging |
0.99 |
|