Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
G |
A |
5: 109,885,259 (GRCm39) |
R200C |
probably benign |
Het |
Ak7 |
G |
A |
12: 105,679,834 (GRCm39) |
V123M |
probably benign |
Het |
Aoc1l1 |
A |
T |
6: 48,952,090 (GRCm39) |
Q5L |
probably benign |
Het |
Apc |
T |
C |
18: 34,451,618 (GRCm39) |
L2804P |
probably damaging |
Het |
Apob |
C |
A |
12: 8,061,331 (GRCm39) |
A3271E |
probably damaging |
Het |
Asl |
G |
T |
5: 130,047,157 (GRCm39) |
A147E |
probably damaging |
Het |
Atp1a1 |
A |
G |
3: 101,494,259 (GRCm39) |
V447A |
probably benign |
Het |
AY358078 |
T |
A |
14: 52,063,532 (GRCm39) |
C393S |
possibly damaging |
Het |
Bcl11b |
T |
C |
12: 107,882,789 (GRCm39) |
K509E |
probably damaging |
Het |
Btnl1 |
T |
C |
17: 34,598,699 (GRCm39) |
I105T |
probably damaging |
Het |
Btnl10 |
A |
G |
11: 58,811,183 (GRCm39) |
T169A |
probably damaging |
Het |
C8b |
T |
C |
4: 104,647,841 (GRCm39) |
I278T |
probably damaging |
Het |
Ccdc66 |
T |
C |
14: 27,222,377 (GRCm39) |
N122S |
probably damaging |
Het |
Cd8b1 |
T |
C |
6: 71,309,459 (GRCm39) |
V181A |
probably benign |
Het |
Cdan1 |
A |
T |
2: 120,561,201 (GRCm39) |
V189D |
probably damaging |
Het |
Celf2 |
G |
T |
2: 6,590,831 (GRCm39) |
N279K |
possibly damaging |
Het |
Cfap52 |
T |
C |
11: 67,817,247 (GRCm39) |
N549D |
probably damaging |
Het |
Cmklr1 |
C |
T |
5: 113,752,930 (GRCm39) |
V24M |
probably benign |
Het |
Cntnap4 |
G |
T |
8: 113,500,371 (GRCm39) |
|
probably null |
Het |
Col27a1 |
G |
A |
4: 63,211,743 (GRCm39) |
G91R |
probably damaging |
Het |
Col5a3 |
A |
G |
9: 20,726,192 (GRCm39) |
|
probably benign |
Het |
Dcc |
C |
T |
18: 71,682,069 (GRCm39) |
|
probably null |
Het |
Deaf1 |
T |
A |
7: 140,890,884 (GRCm39) |
T433S |
possibly damaging |
Het |
Dnah8 |
T |
A |
17: 30,903,211 (GRCm39) |
L950H |
probably damaging |
Het |
Dnajc7 |
A |
T |
11: 100,481,803 (GRCm39) |
Y228* |
probably null |
Het |
Eno1b |
T |
C |
18: 48,180,770 (GRCm39) |
V316A |
probably damaging |
Het |
Exoc4 |
T |
C |
6: 33,415,340 (GRCm39) |
M404T |
possibly damaging |
Het |
Fignl1 |
A |
T |
11: 11,751,268 (GRCm39) |
C596S |
probably benign |
Het |
Fn1 |
A |
C |
1: 71,663,337 (GRCm39) |
Y1050* |
probably null |
Het |
Frem2 |
A |
G |
3: 53,455,228 (GRCm39) |
L2116S |
possibly damaging |
Het |
Gba2 |
T |
A |
4: 43,568,092 (GRCm39) |
S732C |
probably damaging |
Het |
Gcnt4 |
C |
A |
13: 97,082,990 (GRCm39) |
S95R |
probably benign |
Het |
Gpr37 |
A |
G |
6: 25,669,623 (GRCm39) |
V407A |
probably benign |
Het |
Gria2 |
A |
T |
3: 80,599,799 (GRCm39) |
M695K |
probably damaging |
Het |
Hoxa9 |
T |
C |
6: 52,202,690 (GRCm39) |
K132R |
probably damaging |
Het |
Ifi213 |
T |
A |
1: 173,417,480 (GRCm39) |
T311S |
possibly damaging |
Het |
Itgb2 |
T |
A |
10: 77,385,884 (GRCm39) |
N282K |
probably damaging |
Het |
Kcnh8 |
A |
T |
17: 52,909,864 (GRCm39) |
Q11L |
probably benign |
Het |
Klk14 |
T |
C |
7: 43,343,781 (GRCm39) |
C163R |
probably damaging |
Het |
Klk1b3 |
T |
A |
7: 43,850,689 (GRCm39) |
W74R |
possibly damaging |
Het |
Krtap13-1 |
G |
T |
16: 88,526,142 (GRCm39) |
C122F |
possibly damaging |
Het |
Luzp2 |
T |
C |
7: 54,713,104 (GRCm39) |
|
probably null |
Het |
Mbtps1 |
A |
T |
8: 120,262,086 (GRCm39) |
D354E |
probably damaging |
Het |
Mcpt9 |
C |
T |
14: 56,266,049 (GRCm39) |
V60M |
probably damaging |
Het |
Mical3 |
C |
A |
6: 120,911,799 (GRCm39) |
E1083* |
probably null |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Mtor |
T |
A |
4: 148,570,576 (GRCm39) |
V1211E |
probably benign |
Het |
Myb |
T |
A |
10: 21,021,223 (GRCm39) |
D402V |
probably damaging |
Het |
Ncor2 |
G |
A |
5: 125,107,923 (GRCm39) |
T1593I |
probably damaging |
Het |
Ndst3 |
A |
G |
3: 123,465,198 (GRCm39) |
I258T |
probably benign |
Het |
Npy6r |
C |
A |
18: 44,409,468 (GRCm39) |
H296Q |
probably damaging |
Het |
Olfml2b |
T |
A |
1: 170,472,516 (GRCm39) |
L9H |
probably damaging |
Het |
Or10a3n |
A |
G |
7: 108,493,324 (GRCm39) |
C97R |
probably damaging |
Het |
Or1a1b |
A |
T |
11: 74,097,361 (GRCm39) |
V227D |
possibly damaging |
Het |
Or2w2 |
A |
T |
13: 21,757,744 (GRCm39) |
V294D |
probably damaging |
Het |
Or4k15 |
C |
A |
14: 50,364,530 (GRCm39) |
N165K |
probably benign |
Het |
Or5b119 |
C |
T |
19: 13,457,376 (GRCm39) |
C62Y |
probably damaging |
Het |
Or5b94 |
T |
A |
19: 12,652,318 (GRCm39) |
Y250N |
probably damaging |
Het |
Or6c207 |
G |
A |
10: 129,104,274 (GRCm39) |
A306V |
probably benign |
Het |
Or8b8 |
T |
A |
9: 37,809,622 (GRCm39) |
S307R |
probably benign |
Het |
Ovgp1 |
T |
C |
3: 105,893,883 (GRCm39) |
|
probably benign |
Het |
Parg |
G |
A |
14: 31,996,821 (GRCm39) |
R304Q |
probably damaging |
Het |
Pdf |
T |
G |
8: 107,775,167 (GRCm39) |
S22R |
probably benign |
Het |
Phlpp2 |
A |
T |
8: 110,603,515 (GRCm39) |
R60S |
possibly damaging |
Het |
Piwil2 |
C |
T |
14: 70,639,646 (GRCm39) |
E401K |
probably benign |
Het |
Pla2g4e |
T |
G |
2: 120,016,863 (GRCm39) |
H226P |
possibly damaging |
Het |
Polr3a |
T |
C |
14: 24,502,576 (GRCm39) |
|
probably null |
Het |
Ppp3cb |
T |
C |
14: 20,570,714 (GRCm39) |
N339S |
possibly damaging |
Het |
Ptch2 |
G |
A |
4: 116,967,575 (GRCm39) |
D748N |
probably benign |
Het |
Rai14 |
A |
C |
15: 10,592,224 (GRCm39) |
Y224D |
probably damaging |
Het |
Rft1 |
A |
G |
14: 30,411,747 (GRCm39) |
I432V |
probably damaging |
Het |
Rictor |
C |
T |
15: 6,816,625 (GRCm39) |
A1299V |
possibly damaging |
Het |
Sall2 |
A |
G |
14: 52,551,210 (GRCm39) |
C662R |
probably damaging |
Het |
Scn4b |
A |
G |
9: 45,061,737 (GRCm39) |
N208D |
probably damaging |
Het |
Sdhb |
G |
A |
4: 140,700,226 (GRCm39) |
G109R |
probably damaging |
Het |
Sec16a |
A |
G |
2: 26,331,817 (GRCm39) |
V66A |
probably benign |
Het |
Sema4g |
A |
G |
19: 44,990,051 (GRCm39) |
Y710C |
probably damaging |
Het |
Serpinb12 |
T |
A |
1: 106,876,883 (GRCm39) |
D66E |
probably benign |
Het |
Shc4 |
T |
A |
2: 125,497,602 (GRCm39) |
D369V |
probably benign |
Het |
Siglech |
T |
C |
7: 55,421,441 (GRCm39) |
L285P |
probably damaging |
Het |
Skint6 |
A |
G |
4: 112,931,273 (GRCm39) |
M506T |
probably benign |
Het |
Slco1a6 |
C |
A |
6: 142,047,378 (GRCm39) |
C404F |
probably benign |
Het |
Slfn14 |
T |
A |
11: 83,174,140 (GRCm39) |
K284* |
probably null |
Het |
Sox14 |
A |
G |
9: 99,757,715 (GRCm39) |
I8T |
probably damaging |
Het |
Srpk3 |
A |
G |
X: 72,818,547 (GRCm39) |
H79R |
possibly damaging |
Het |
Tdpoz3 |
A |
T |
3: 93,734,330 (GRCm39) |
H335L |
probably damaging |
Het |
Tdrd5 |
T |
A |
1: 156,111,944 (GRCm39) |
T479S |
probably benign |
Het |
Tnik |
T |
C |
3: 28,596,249 (GRCm39) |
|
probably null |
Het |
Tnpo2 |
T |
C |
8: 85,780,432 (GRCm39) |
S720P |
probably benign |
Het |
Tpst1 |
A |
G |
5: 130,130,547 (GRCm39) |
K6E |
probably damaging |
Het |
Trank1 |
T |
A |
9: 111,191,329 (GRCm39) |
I446N |
probably damaging |
Het |
Trmt44 |
A |
T |
5: 35,732,351 (GRCm39) |
D13E |
probably benign |
Het |
Ubr4 |
T |
A |
4: 139,126,890 (GRCm39) |
V471E |
possibly damaging |
Het |
Ubtd1 |
A |
G |
19: 42,022,030 (GRCm39) |
T101A |
probably benign |
Het |
Zbtb7c |
C |
T |
18: 76,269,918 (GRCm39) |
A2V |
possibly damaging |
Het |
Zfp423 |
C |
T |
8: 88,414,709 (GRCm39) |
G1182D |
possibly damaging |
Het |
Zfp618 |
G |
A |
4: 63,051,216 (GRCm39) |
V666M |
probably damaging |
Het |
Zmat1 |
A |
T |
X: 133,873,694 (GRCm39) |
S566T |
probably damaging |
Homo |
Zscan20 |
T |
C |
4: 128,481,899 (GRCm39) |
T588A |
probably benign |
Het |
Zscan25 |
G |
A |
5: 145,227,926 (GRCm39) |
R530H |
probably damaging |
Het |
|
Other mutations in Ugt3a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00912:Ugt3a1
|
APN |
15 |
9,310,698 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01109:Ugt3a1
|
APN |
15 |
9,367,354 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01131:Ugt3a1
|
APN |
15 |
9,365,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01627:Ugt3a1
|
APN |
15 |
9,335,806 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01746:Ugt3a1
|
APN |
15 |
9,361,754 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01752:Ugt3a1
|
APN |
15 |
9,306,232 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01949:Ugt3a1
|
APN |
15 |
9,335,815 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02213:Ugt3a1
|
APN |
15 |
9,370,310 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02407:Ugt3a1
|
APN |
15 |
9,365,316 (GRCm39) |
nonsense |
probably null |
|
IGL02438:Ugt3a1
|
APN |
15 |
9,292,062 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02588:Ugt3a1
|
APN |
15 |
9,361,542 (GRCm39) |
missense |
probably benign |
|
IGL02894:Ugt3a1
|
APN |
15 |
9,367,487 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02966:Ugt3a1
|
APN |
15 |
9,370,154 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03385:Ugt3a1
|
APN |
15 |
9,338,824 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03493:Ugt3a1
|
APN |
15 |
9,361,569 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4354001:Ugt3a1
|
UTSW |
15 |
9,306,446 (GRCm39) |
nonsense |
probably null |
|
R0127:Ugt3a1
|
UTSW |
15 |
9,306,342 (GRCm39) |
missense |
probably benign |
0.01 |
R0554:Ugt3a1
|
UTSW |
15 |
9,351,206 (GRCm39) |
missense |
probably benign |
0.14 |
R0647:Ugt3a1
|
UTSW |
15 |
9,310,635 (GRCm39) |
missense |
probably benign |
0.00 |
R0833:Ugt3a1
|
UTSW |
15 |
9,370,236 (GRCm39) |
missense |
probably damaging |
0.96 |
R0841:Ugt3a1
|
UTSW |
15 |
9,306,214 (GRCm39) |
missense |
probably benign |
0.07 |
R1071:Ugt3a1
|
UTSW |
15 |
9,367,454 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1395:Ugt3a1
|
UTSW |
15 |
9,306,378 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1513:Ugt3a1
|
UTSW |
15 |
9,361,610 (GRCm39) |
missense |
probably benign |
0.07 |
R1616:Ugt3a1
|
UTSW |
15 |
9,306,330 (GRCm39) |
nonsense |
probably null |
|
R1844:Ugt3a1
|
UTSW |
15 |
9,351,254 (GRCm39) |
missense |
probably benign |
0.07 |
R1874:Ugt3a1
|
UTSW |
15 |
9,365,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R2305:Ugt3a1
|
UTSW |
15 |
9,351,203 (GRCm39) |
missense |
probably benign |
|
R2338:Ugt3a1
|
UTSW |
15 |
9,292,059 (GRCm39) |
splice site |
probably benign |
|
R3052:Ugt3a1
|
UTSW |
15 |
9,365,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R3755:Ugt3a1
|
UTSW |
15 |
9,367,498 (GRCm39) |
missense |
probably benign |
0.21 |
R3797:Ugt3a1
|
UTSW |
15 |
9,310,727 (GRCm39) |
nonsense |
probably null |
|
R3945:Ugt3a1
|
UTSW |
15 |
9,370,184 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4135:Ugt3a1
|
UTSW |
15 |
9,338,810 (GRCm39) |
missense |
probably damaging |
0.98 |
R4261:Ugt3a1
|
UTSW |
15 |
9,335,879 (GRCm39) |
splice site |
probably null |
|
R4305:Ugt3a1
|
UTSW |
15 |
9,306,360 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4385:Ugt3a1
|
UTSW |
15 |
9,306,565 (GRCm39) |
missense |
probably benign |
0.15 |
R4438:Ugt3a1
|
UTSW |
15 |
9,351,283 (GRCm39) |
missense |
probably benign |
0.01 |
R4570:Ugt3a1
|
UTSW |
15 |
9,338,807 (GRCm39) |
missense |
probably benign |
0.12 |
R4572:Ugt3a1
|
UTSW |
15 |
9,306,479 (GRCm39) |
missense |
probably benign |
0.00 |
R4744:Ugt3a1
|
UTSW |
15 |
9,310,639 (GRCm39) |
missense |
probably benign |
0.36 |
R4791:Ugt3a1
|
UTSW |
15 |
9,361,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R4957:Ugt3a1
|
UTSW |
15 |
9,365,274 (GRCm39) |
missense |
probably benign |
0.27 |
R5011:Ugt3a1
|
UTSW |
15 |
9,365,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R5035:Ugt3a1
|
UTSW |
15 |
9,361,704 (GRCm39) |
missense |
probably benign |
0.01 |
R5554:Ugt3a1
|
UTSW |
15 |
9,370,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R5573:Ugt3a1
|
UTSW |
15 |
9,361,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R5631:Ugt3a1
|
UTSW |
15 |
9,361,971 (GRCm39) |
missense |
probably damaging |
0.98 |
R5696:Ugt3a1
|
UTSW |
15 |
9,361,534 (GRCm39) |
splice site |
silent |
|
R5715:Ugt3a1
|
UTSW |
15 |
9,306,430 (GRCm39) |
missense |
probably damaging |
0.96 |
R6036:Ugt3a1
|
UTSW |
15 |
9,306,172 (GRCm39) |
missense |
probably benign |
0.01 |
R6036:Ugt3a1
|
UTSW |
15 |
9,306,172 (GRCm39) |
missense |
probably benign |
0.01 |
R6156:Ugt3a1
|
UTSW |
15 |
9,310,762 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6228:Ugt3a1
|
UTSW |
15 |
9,310,726 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6265:Ugt3a1
|
UTSW |
15 |
9,361,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Ugt3a1
|
UTSW |
15 |
9,365,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R6311:Ugt3a1
|
UTSW |
15 |
9,361,604 (GRCm39) |
nonsense |
probably null |
|
R6344:Ugt3a1
|
UTSW |
15 |
9,306,317 (GRCm39) |
missense |
probably damaging |
0.98 |
R6380:Ugt3a1
|
UTSW |
15 |
9,306,541 (GRCm39) |
missense |
probably benign |
0.00 |
R6383:Ugt3a1
|
UTSW |
15 |
9,306,541 (GRCm39) |
missense |
probably benign |
0.00 |
R6680:Ugt3a1
|
UTSW |
15 |
9,370,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6737:Ugt3a1
|
UTSW |
15 |
9,311,895 (GRCm39) |
missense |
probably benign |
0.30 |
R6848:Ugt3a1
|
UTSW |
15 |
9,280,138 (GRCm39) |
splice site |
probably null |
|
R6937:Ugt3a1
|
UTSW |
15 |
9,292,158 (GRCm39) |
missense |
probably benign |
0.00 |
R7061:Ugt3a1
|
UTSW |
15 |
9,306,240 (GRCm39) |
missense |
probably benign |
0.12 |
R7672:Ugt3a1
|
UTSW |
15 |
9,310,779 (GRCm39) |
nonsense |
probably null |
|
R7840:Ugt3a1
|
UTSW |
15 |
9,311,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R7945:Ugt3a1
|
UTSW |
15 |
9,284,261 (GRCm39) |
critical splice donor site |
probably null |
|
R8105:Ugt3a1
|
UTSW |
15 |
9,306,476 (GRCm39) |
missense |
probably benign |
0.00 |
R8229:Ugt3a1
|
UTSW |
15 |
9,367,463 (GRCm39) |
missense |
probably damaging |
0.99 |
R8296:Ugt3a1
|
UTSW |
15 |
9,362,024 (GRCm39) |
missense |
probably benign |
0.18 |
R8414:Ugt3a1
|
UTSW |
15 |
9,310,669 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8809:Ugt3a1
|
UTSW |
15 |
9,367,345 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8981:Ugt3a1
|
UTSW |
15 |
9,312,014 (GRCm39) |
missense |
probably benign |
0.20 |
R9066:Ugt3a1
|
UTSW |
15 |
9,367,384 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9071:Ugt3a1
|
UTSW |
15 |
9,370,224 (GRCm39) |
nonsense |
probably null |
|
R9111:Ugt3a1
|
UTSW |
15 |
9,306,333 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9151:Ugt3a1
|
UTSW |
15 |
9,362,051 (GRCm39) |
missense |
probably benign |
0.03 |
R9451:Ugt3a1
|
UTSW |
15 |
9,292,158 (GRCm39) |
missense |
probably benign |
0.00 |
R9522:Ugt3a1
|
UTSW |
15 |
9,370,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R9567:Ugt3a1
|
UTSW |
15 |
9,306,370 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9609:Ugt3a1
|
UTSW |
15 |
9,361,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R9657:Ugt3a1
|
UTSW |
15 |
9,280,133 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Ugt3a1
|
UTSW |
15 |
9,367,343 (GRCm39) |
missense |
probably benign |
0.02 |
|