Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
A |
G |
7: 40,644,149 (GRCm39) |
Y606C |
probably benign |
Het |
Acad9 |
A |
G |
3: 36,139,630 (GRCm39) |
Y410C |
probably damaging |
Het |
Acot6 |
C |
T |
12: 84,156,149 (GRCm39) |
P366S |
probably damaging |
Het |
Adrm1b |
T |
C |
3: 92,336,315 (GRCm39) |
|
probably benign |
Het |
Anks1 |
G |
T |
17: 28,273,273 (GRCm39) |
G964V |
probably damaging |
Het |
Apol7a |
A |
T |
15: 77,274,176 (GRCm39) |
|
probably benign |
Het |
Arid3c |
G |
A |
4: 41,725,087 (GRCm39) |
A320V |
probably damaging |
Het |
Bnip3l |
A |
T |
14: 67,237,101 (GRCm39) |
N50K |
probably benign |
Het |
C1qtnf4 |
C |
A |
2: 90,720,297 (GRCm39) |
A190D |
probably benign |
Het |
Calhm5 |
A |
T |
10: 33,972,189 (GRCm39) |
M82K |
probably benign |
Het |
Cdcp3 |
G |
T |
7: 130,824,400 (GRCm39) |
W165L |
probably damaging |
Het |
Cdh1 |
G |
T |
8: 107,387,545 (GRCm39) |
V482L |
probably benign |
Het |
Cdrt4 |
A |
C |
11: 62,883,486 (GRCm39) |
I63L |
probably benign |
Het |
Cic |
A |
T |
7: 24,970,736 (GRCm39) |
T156S |
possibly damaging |
Het |
Ckm |
A |
G |
7: 19,154,156 (GRCm39) |
N301S |
probably benign |
Het |
Colgalt1 |
C |
T |
8: 72,076,165 (GRCm39) |
R539C |
probably damaging |
Het |
Cop1 |
A |
G |
1: 159,134,154 (GRCm39) |
D132G |
probably damaging |
Het |
Cpd |
G |
T |
11: 76,675,881 (GRCm39) |
N1257K |
probably benign |
Het |
Cyp2c67 |
T |
C |
19: 39,604,123 (GRCm39) |
H411R |
probably damaging |
Het |
Cyp2r1 |
A |
T |
7: 114,152,316 (GRCm39) |
F5I |
probably damaging |
Het |
Dnah7c |
A |
T |
1: 46,494,973 (GRCm39) |
Q67L |
probably benign |
Het |
Dnm1l |
C |
A |
16: 16,147,671 (GRCm39) |
E365* |
probably null |
Het |
Dst |
A |
T |
1: 34,205,315 (GRCm39) |
I502F |
probably damaging |
Het |
Espl1 |
T |
C |
15: 102,212,535 (GRCm39) |
V547A |
possibly damaging |
Het |
Foxa1 |
C |
T |
12: 57,589,264 (GRCm39) |
A319T |
probably benign |
Het |
Frem1 |
G |
T |
4: 82,904,838 (GRCm39) |
H859N |
probably damaging |
Het |
Frem3 |
T |
A |
8: 81,339,208 (GRCm39) |
D500E |
probably damaging |
Het |
Gpatch2l |
G |
A |
12: 86,290,958 (GRCm39) |
R47H |
probably damaging |
Het |
Grip1 |
A |
G |
10: 119,822,375 (GRCm39) |
D394G |
probably damaging |
Het |
Gsap |
C |
A |
5: 21,476,235 (GRCm39) |
T589K |
possibly damaging |
Het |
Gsg1l |
A |
G |
7: 125,522,658 (GRCm39) |
V190A |
probably damaging |
Het |
Kcnmb1 |
A |
T |
11: 33,920,131 (GRCm39) |
T115S |
probably benign |
Het |
Kirrel2 |
A |
C |
7: 30,154,604 (GRCm39) |
F169C |
probably damaging |
Het |
L3mbtl1 |
C |
T |
2: 162,803,368 (GRCm39) |
T397M |
probably damaging |
Het |
Lama1 |
G |
A |
17: 68,060,820 (GRCm39) |
C716Y |
|
Het |
Lamc2 |
G |
A |
1: 153,012,508 (GRCm39) |
T722M |
probably benign |
Het |
Lrig1 |
T |
C |
6: 94,588,610 (GRCm39) |
D513G |
possibly damaging |
Het |
Lrrk1 |
T |
C |
7: 65,942,090 (GRCm39) |
D716G |
probably damaging |
Het |
Matn4 |
G |
A |
2: 164,231,584 (GRCm39) |
R582* |
probably null |
Het |
Mdn1 |
A |
T |
4: 32,733,374 (GRCm39) |
R3133W |
probably benign |
Het |
Mmp7 |
A |
G |
9: 7,695,489 (GRCm39) |
D122G |
probably damaging |
Het |
Naaladl1 |
A |
G |
19: 6,165,578 (GRCm39) |
D744G |
possibly damaging |
Het |
Nampt |
T |
G |
12: 32,898,742 (GRCm39) |
Y453D |
probably benign |
Het |
Nlrp12 |
A |
G |
7: 3,288,481 (GRCm39) |
V677A |
probably benign |
Het |
Ntng2 |
T |
C |
2: 29,087,080 (GRCm39) |
N414S |
probably damaging |
Het |
Or1e16 |
A |
G |
11: 73,286,410 (GRCm39) |
V146A |
probably benign |
Het |
Or4g17 |
A |
G |
2: 111,209,708 (GRCm39) |
D121G |
probably damaging |
Het |
Or5p52 |
A |
G |
7: 107,502,829 (GRCm39) |
R302G |
probably benign |
Het |
Or9m1b |
A |
C |
2: 87,836,529 (GRCm39) |
F189V |
probably benign |
Het |
Parp4 |
A |
C |
14: 56,851,196 (GRCm39) |
Q733P |
probably damaging |
Het |
Pdcl3 |
G |
A |
1: 39,034,417 (GRCm39) |
V56I |
probably benign |
Het |
Pepd |
A |
G |
7: 34,721,144 (GRCm39) |
Y256C |
probably damaging |
Het |
Plg |
G |
T |
17: 12,637,938 (GRCm39) |
R788L |
probably benign |
Het |
Plod1 |
A |
T |
4: 148,000,675 (GRCm39) |
|
probably benign |
Het |
Ptprc |
A |
G |
1: 138,016,482 (GRCm39) |
V513A |
probably damaging |
Het |
Pxdn |
T |
C |
12: 30,045,370 (GRCm39) |
I373T |
possibly damaging |
Het |
Qrfprl |
A |
T |
6: 65,418,285 (GRCm39) |
K151I |
probably damaging |
Het |
Rbbp8 |
G |
A |
18: 11,851,965 (GRCm39) |
G262E |
probably damaging |
Het |
Rfc2 |
T |
A |
5: 134,623,104 (GRCm39) |
Y240* |
probably null |
Het |
Rps15 |
A |
G |
10: 80,129,598 (GRCm39) |
E71G |
possibly damaging |
Het |
Rsrc1 |
C |
T |
3: 66,901,982 (GRCm39) |
P44L |
unknown |
Het |
Ryr1 |
A |
C |
7: 28,793,607 (GRCm39) |
M1287R |
probably damaging |
Het |
Scart2 |
G |
A |
7: 139,841,514 (GRCm39) |
D273N |
probably benign |
Het |
Serpina9 |
A |
G |
12: 103,967,495 (GRCm39) |
L300P |
probably damaging |
Het |
Sh3rf2 |
G |
A |
18: 42,234,606 (GRCm39) |
A130T |
probably damaging |
Het |
Slc12a8 |
G |
A |
16: 33,355,263 (GRCm39) |
W26* |
probably null |
Het |
Snx18 |
A |
T |
13: 113,731,265 (GRCm39) |
H576Q |
probably damaging |
Het |
Tagln3 |
G |
A |
16: 45,543,321 (GRCm39) |
T107I |
probably benign |
Het |
Thap1 |
C |
A |
8: 26,652,679 (GRCm39) |
T139K |
probably damaging |
Het |
Tle4 |
T |
A |
19: 14,541,817 (GRCm39) |
|
probably null |
Het |
Tmem87a |
A |
T |
2: 120,193,409 (GRCm39) |
M502K |
possibly damaging |
Het |
Tpcn2 |
A |
T |
7: 144,810,522 (GRCm39) |
V605E |
probably benign |
Het |
Trgj1 |
C |
A |
13: 19,394,529 (GRCm39) |
|
probably benign |
Het |
Tsc2 |
A |
T |
17: 24,847,028 (GRCm39) |
V179E |
probably damaging |
Het |
Ubap2l |
T |
C |
3: 89,916,548 (GRCm39) |
T909A |
probably damaging |
Het |
Ubl4b |
T |
G |
3: 107,462,140 (GRCm39) |
Q40P |
probably damaging |
Het |
Vmn1r229 |
A |
G |
17: 21,035,277 (GRCm39) |
D174G |
probably damaging |
Het |
Vmn2r50 |
A |
T |
7: 9,779,964 (GRCm39) |
Y472* |
probably null |
Het |
Vmn2r74 |
T |
A |
7: 85,601,943 (GRCm39) |
D565V |
probably benign |
Het |
Vmn2r74 |
T |
A |
7: 85,606,860 (GRCm39) |
|
probably null |
Het |
Vmn2r82 |
T |
A |
10: 79,232,377 (GRCm39) |
V792E |
probably damaging |
Het |
Zfp335 |
G |
A |
2: 164,735,210 (GRCm39) |
Q1179* |
probably null |
Het |
Zmynd12 |
A |
C |
4: 119,310,772 (GRCm39) |
K327Q |
probably benign |
Het |
Zwilch |
G |
A |
9: 64,072,731 (GRCm39) |
Q27* |
probably null |
Het |
|
Other mutations in Dclk3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02027:Dclk3
|
APN |
9 |
111,296,911 (GRCm39) |
nonsense |
probably null |
|
IGL02125:Dclk3
|
APN |
9 |
111,298,175 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02547:Dclk3
|
APN |
9 |
111,298,091 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03393:Dclk3
|
APN |
9 |
111,317,741 (GRCm39) |
utr 3 prime |
probably benign |
|
G1citation:Dclk3
|
UTSW |
9 |
111,268,405 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02984:Dclk3
|
UTSW |
9 |
111,317,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Dclk3
|
UTSW |
9 |
111,296,738 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0109:Dclk3
|
UTSW |
9 |
111,296,738 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0238:Dclk3
|
UTSW |
9 |
111,311,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R0238:Dclk3
|
UTSW |
9 |
111,311,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R0432:Dclk3
|
UTSW |
9 |
111,314,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R0440:Dclk3
|
UTSW |
9 |
111,298,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R0530:Dclk3
|
UTSW |
9 |
111,311,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R1024:Dclk3
|
UTSW |
9 |
111,298,138 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1443:Dclk3
|
UTSW |
9 |
111,298,088 (GRCm39) |
missense |
probably benign |
0.01 |
R1474:Dclk3
|
UTSW |
9 |
111,298,304 (GRCm39) |
missense |
probably benign |
0.43 |
R1479:Dclk3
|
UTSW |
9 |
111,297,614 (GRCm39) |
missense |
probably benign |
|
R1482:Dclk3
|
UTSW |
9 |
111,296,888 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1543:Dclk3
|
UTSW |
9 |
111,297,122 (GRCm39) |
missense |
probably benign |
0.04 |
R1552:Dclk3
|
UTSW |
9 |
111,317,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R1559:Dclk3
|
UTSW |
9 |
111,298,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:Dclk3
|
UTSW |
9 |
111,297,422 (GRCm39) |
missense |
probably benign |
0.00 |
R2369:Dclk3
|
UTSW |
9 |
111,317,610 (GRCm39) |
missense |
probably benign |
0.16 |
R4111:Dclk3
|
UTSW |
9 |
111,298,148 (GRCm39) |
missense |
probably damaging |
0.99 |
R4510:Dclk3
|
UTSW |
9 |
111,297,060 (GRCm39) |
missense |
probably benign |
0.01 |
R4511:Dclk3
|
UTSW |
9 |
111,297,060 (GRCm39) |
missense |
probably benign |
0.01 |
R4592:Dclk3
|
UTSW |
9 |
111,296,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4604:Dclk3
|
UTSW |
9 |
111,298,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Dclk3
|
UTSW |
9 |
111,297,716 (GRCm39) |
missense |
probably benign |
|
R4932:Dclk3
|
UTSW |
9 |
111,297,110 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5045:Dclk3
|
UTSW |
9 |
111,296,856 (GRCm39) |
missense |
probably damaging |
0.99 |
R5233:Dclk3
|
UTSW |
9 |
111,297,749 (GRCm39) |
missense |
probably benign |
|
R5338:Dclk3
|
UTSW |
9 |
111,298,127 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5463:Dclk3
|
UTSW |
9 |
111,298,328 (GRCm39) |
missense |
probably benign |
0.26 |
R6822:Dclk3
|
UTSW |
9 |
111,268,405 (GRCm39) |
missense |
probably benign |
0.03 |
R7187:Dclk3
|
UTSW |
9 |
111,314,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R7532:Dclk3
|
UTSW |
9 |
111,296,596 (GRCm39) |
missense |
probably benign |
0.03 |
R7534:Dclk3
|
UTSW |
9 |
111,297,286 (GRCm39) |
missense |
probably benign |
|
R7734:Dclk3
|
UTSW |
9 |
111,298,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R8326:Dclk3
|
UTSW |
9 |
111,296,602 (GRCm39) |
missense |
probably damaging |
0.96 |
R8372:Dclk3
|
UTSW |
9 |
111,314,081 (GRCm39) |
missense |
probably damaging |
0.98 |
R8388:Dclk3
|
UTSW |
9 |
111,311,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R8423:Dclk3
|
UTSW |
9 |
111,297,787 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8493:Dclk3
|
UTSW |
9 |
111,297,215 (GRCm39) |
missense |
probably benign |
0.06 |
R9013:Dclk3
|
UTSW |
9 |
111,297,566 (GRCm39) |
missense |
probably benign |
0.31 |
R9114:Dclk3
|
UTSW |
9 |
111,317,683 (GRCm39) |
missense |
probably benign |
0.06 |
R9338:Dclk3
|
UTSW |
9 |
111,268,373 (GRCm39) |
missense |
unknown |
|
R9412:Dclk3
|
UTSW |
9 |
111,311,819 (GRCm39) |
critical splice donor site |
probably null |
|
R9701:Dclk3
|
UTSW |
9 |
111,298,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R9776:Dclk3
|
UTSW |
9 |
111,298,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R9802:Dclk3
|
UTSW |
9 |
111,298,244 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Dclk3
|
UTSW |
9 |
111,314,143 (GRCm39) |
missense |
probably damaging |
1.00 |
|