Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acat1 |
A |
C |
9: 53,506,062 (GRCm39) |
V86G |
probably benign |
Het |
Adgra3 |
A |
T |
5: 50,174,194 (GRCm39) |
W115R |
probably benign |
Het |
Ahr |
G |
A |
12: 35,554,709 (GRCm39) |
A470V |
probably benign |
Het |
Aoah |
A |
T |
13: 21,000,752 (GRCm39) |
Q62L |
possibly damaging |
Het |
Arhgef12 |
A |
T |
9: 42,937,524 (GRCm39) |
D100E |
possibly damaging |
Het |
Asic1 |
A |
G |
15: 99,570,038 (GRCm39) |
N120D |
probably benign |
Het |
Atp2b2 |
A |
G |
6: 113,736,103 (GRCm39) |
L988P |
probably damaging |
Het |
Atxn2 |
T |
A |
5: 121,948,972 (GRCm39) |
H789Q |
probably damaging |
Het |
Clk1 |
G |
T |
1: 58,460,261 (GRCm39) |
S123* |
probably null |
Het |
Col10a1 |
C |
T |
10: 34,271,012 (GRCm39) |
A328V |
probably benign |
Het |
Col26a1 |
G |
T |
5: 136,771,972 (GRCm39) |
D415E |
possibly damaging |
Het |
Ctla2a |
A |
G |
13: 61,083,273 (GRCm39) |
|
probably benign |
Het |
Cwf19l2 |
A |
G |
9: 3,430,622 (GRCm39) |
E318G |
probably benign |
Het |
Dnajc16 |
C |
T |
4: 141,495,043 (GRCm39) |
W523* |
probably null |
Het |
Ehhadh |
T |
C |
16: 21,581,144 (GRCm39) |
E616G |
probably damaging |
Het |
F5 |
A |
T |
1: 164,020,569 (GRCm39) |
K1015* |
probably null |
Het |
Fam78a |
A |
G |
2: 31,972,894 (GRCm39) |
W9R |
possibly damaging |
Het |
Frs2 |
A |
T |
10: 116,909,838 (GRCm39) |
M508K |
possibly damaging |
Het |
Gm3164 |
A |
T |
14: 4,440,111 (GRCm38) |
M200L |
probably benign |
Het |
Gm44511 |
T |
C |
6: 128,757,358 (GRCm39) |
S179G |
probably damaging |
Het |
Gpr25 |
G |
A |
1: 136,188,550 (GRCm39) |
S21L |
probably benign |
Het |
Hsdl2 |
A |
G |
4: 59,594,471 (GRCm39) |
D34G |
probably damaging |
Het |
Kcnt1 |
A |
G |
2: 25,799,215 (GRCm39) |
|
probably null |
Het |
Kl |
A |
G |
5: 150,915,015 (GRCm39) |
Y914C |
probably damaging |
Het |
Map3k3 |
T |
G |
11: 106,001,577 (GRCm39) |
V45G |
probably damaging |
Het |
Mppe1 |
A |
C |
18: 67,360,755 (GRCm39) |
C261W |
probably damaging |
Het |
Nin |
T |
C |
12: 70,082,044 (GRCm39) |
T1640A |
probably benign |
Het |
Or51a8 |
T |
A |
7: 102,550,036 (GRCm39) |
I154N |
possibly damaging |
Het |
Or51ac3 |
A |
G |
7: 103,213,796 (GRCm39) |
|
probably null |
Het |
Or5c1 |
C |
T |
2: 37,221,968 (GRCm39) |
L70F |
probably damaging |
Het |
Or5p59 |
T |
A |
7: 107,703,380 (GRCm39) |
M288K |
probably damaging |
Het |
Or7g26 |
A |
T |
9: 19,230,664 (GRCm39) |
Y284F |
probably damaging |
Het |
Oxr1 |
A |
G |
15: 41,680,559 (GRCm39) |
N166D |
probably damaging |
Het |
Pank4 |
T |
A |
4: 155,054,442 (GRCm39) |
|
probably benign |
Het |
Pgd |
A |
G |
4: 149,246,084 (GRCm39) |
|
probably null |
Het |
Pitrm1 |
C |
T |
13: 6,624,429 (GRCm39) |
H831Y |
probably benign |
Het |
Pkd1l2 |
G |
A |
8: 117,792,484 (GRCm39) |
T436I |
probably benign |
Het |
Rad51 |
A |
C |
2: 118,946,795 (GRCm39) |
M1L |
possibly damaging |
Het |
Recql5 |
G |
T |
11: 115,785,257 (GRCm39) |
S746R |
possibly damaging |
Het |
Rhbdl3 |
C |
T |
11: 80,214,287 (GRCm39) |
Q133* |
probably null |
Het |
Rpp40 |
A |
T |
13: 36,088,494 (GRCm39) |
L59Q |
probably damaging |
Het |
Rtca |
C |
A |
3: 116,286,741 (GRCm39) |
|
probably benign |
Het |
Rtkn |
C |
T |
6: 83,124,853 (GRCm39) |
Q108* |
probably null |
Het |
Shoc1 |
A |
C |
4: 59,094,274 (GRCm39) |
I150S |
possibly damaging |
Het |
Sirt6 |
C |
T |
10: 81,463,375 (GRCm39) |
|
probably benign |
Het |
Slc9a4 |
G |
A |
1: 40,649,537 (GRCm39) |
V517M |
probably benign |
Het |
Smarca2 |
G |
T |
19: 26,655,712 (GRCm39) |
|
probably benign |
Het |
Snx33 |
A |
T |
9: 56,833,735 (GRCm39) |
D111E |
probably benign |
Het |
Tgfb1 |
T |
C |
7: 25,403,621 (GRCm39) |
I311T |
probably damaging |
Het |
Tgfb2 |
C |
T |
1: 186,362,806 (GRCm39) |
|
probably null |
Het |
Tmem232 |
T |
C |
17: 65,563,384 (GRCm39) |
T670A |
probably benign |
Het |
Tnfsf4 |
T |
C |
1: 161,223,213 (GRCm39) |
F21L |
possibly damaging |
Het |
Unc79 |
T |
C |
12: 103,139,785 (GRCm39) |
V2515A |
possibly damaging |
Het |
Utp6 |
T |
C |
11: 79,844,450 (GRCm39) |
K192E |
probably damaging |
Het |
Vmn2r102 |
T |
C |
17: 19,914,328 (GRCm39) |
F631S |
possibly damaging |
Het |
Zfp516 |
A |
C |
18: 82,974,038 (GRCm39) |
I79L |
possibly damaging |
Het |
|
Other mutations in Ubr5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Ubr5
|
APN |
15 |
37,984,280 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00548:Ubr5
|
APN |
15 |
38,004,565 (GRCm39) |
missense |
probably benign |
0.11 |
IGL00675:Ubr5
|
APN |
15 |
38,018,528 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL00770:Ubr5
|
APN |
15 |
38,006,785 (GRCm39) |
missense |
probably benign |
0.27 |
IGL00774:Ubr5
|
APN |
15 |
38,006,785 (GRCm39) |
missense |
probably benign |
0.27 |
IGL00919:Ubr5
|
APN |
15 |
38,041,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00962:Ubr5
|
APN |
15 |
37,986,178 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01328:Ubr5
|
APN |
15 |
37,981,767 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01359:Ubr5
|
APN |
15 |
37,973,250 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01394:Ubr5
|
APN |
15 |
38,009,875 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01674:Ubr5
|
APN |
15 |
37,998,623 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01981:Ubr5
|
APN |
15 |
37,996,842 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01993:Ubr5
|
APN |
15 |
37,973,256 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02159:Ubr5
|
APN |
15 |
37,991,623 (GRCm39) |
splice site |
probably benign |
|
IGL02252:Ubr5
|
APN |
15 |
38,025,138 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02442:Ubr5
|
APN |
15 |
38,038,145 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02502:Ubr5
|
APN |
15 |
38,030,933 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02503:Ubr5
|
APN |
15 |
38,018,558 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02503:Ubr5
|
APN |
15 |
38,018,564 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02546:Ubr5
|
APN |
15 |
38,008,991 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02556:Ubr5
|
APN |
15 |
38,002,692 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02647:Ubr5
|
APN |
15 |
37,992,326 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02679:Ubr5
|
APN |
15 |
38,002,558 (GRCm39) |
missense |
probably benign |
0.36 |
IGL02726:Ubr5
|
APN |
15 |
38,000,806 (GRCm39) |
splice site |
probably benign |
|
IGL02884:Ubr5
|
APN |
15 |
37,998,620 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02972:Ubr5
|
APN |
15 |
38,042,196 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03000:Ubr5
|
APN |
15 |
38,025,096 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03057:Ubr5
|
APN |
15 |
38,041,150 (GRCm39) |
splice site |
probably benign |
|
IGL03085:Ubr5
|
APN |
15 |
38,029,812 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03198:Ubr5
|
APN |
15 |
38,045,964 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03368:Ubr5
|
APN |
15 |
37,998,560 (GRCm39) |
missense |
probably damaging |
0.96 |
Anchovy
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
P0016:Ubr5
|
UTSW |
15 |
38,000,822 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4142001:Ubr5
|
UTSW |
15 |
38,042,153 (GRCm39) |
missense |
|
|
R0133:Ubr5
|
UTSW |
15 |
37,996,815 (GRCm39) |
missense |
probably damaging |
0.98 |
R0173:Ubr5
|
UTSW |
15 |
38,004,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Ubr5
|
UTSW |
15 |
37,968,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Ubr5
|
UTSW |
15 |
37,968,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R0314:Ubr5
|
UTSW |
15 |
37,997,431 (GRCm39) |
missense |
probably damaging |
0.99 |
R0379:Ubr5
|
UTSW |
15 |
38,019,201 (GRCm39) |
missense |
probably benign |
0.00 |
R0390:Ubr5
|
UTSW |
15 |
38,030,916 (GRCm39) |
missense |
probably benign |
0.19 |
R0415:Ubr5
|
UTSW |
15 |
37,973,224 (GRCm39) |
missense |
probably damaging |
0.98 |
R0531:Ubr5
|
UTSW |
15 |
37,991,588 (GRCm39) |
missense |
probably benign |
0.34 |
R0650:Ubr5
|
UTSW |
15 |
38,031,051 (GRCm39) |
splice site |
probably benign |
|
R0720:Ubr5
|
UTSW |
15 |
37,973,235 (GRCm39) |
missense |
probably damaging |
0.98 |
R1183:Ubr5
|
UTSW |
15 |
37,997,419 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1302:Ubr5
|
UTSW |
15 |
38,041,723 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1442:Ubr5
|
UTSW |
15 |
38,015,168 (GRCm39) |
splice site |
probably benign |
|
R1507:Ubr5
|
UTSW |
15 |
37,981,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R1575:Ubr5
|
UTSW |
15 |
38,041,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R1577:Ubr5
|
UTSW |
15 |
38,030,974 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1622:Ubr5
|
UTSW |
15 |
38,009,357 (GRCm39) |
unclassified |
probably benign |
|
R1721:Ubr5
|
UTSW |
15 |
38,042,090 (GRCm39) |
missense |
probably benign |
0.18 |
R1799:Ubr5
|
UTSW |
15 |
37,989,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Ubr5
|
UTSW |
15 |
37,981,161 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1867:Ubr5
|
UTSW |
15 |
38,042,090 (GRCm39) |
missense |
probably benign |
0.18 |
R1868:Ubr5
|
UTSW |
15 |
38,042,090 (GRCm39) |
missense |
probably benign |
0.18 |
R2065:Ubr5
|
UTSW |
15 |
38,041,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R2107:Ubr5
|
UTSW |
15 |
37,989,546 (GRCm39) |
missense |
probably benign |
0.00 |
R2201:Ubr5
|
UTSW |
15 |
38,002,543 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2261:Ubr5
|
UTSW |
15 |
37,988,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R2441:Ubr5
|
UTSW |
15 |
37,989,589 (GRCm39) |
missense |
probably damaging |
0.99 |
R2512:Ubr5
|
UTSW |
15 |
38,002,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R3008:Ubr5
|
UTSW |
15 |
38,031,089 (GRCm39) |
missense |
probably benign |
|
R3412:Ubr5
|
UTSW |
15 |
38,004,479 (GRCm39) |
splice site |
probably benign |
|
R3898:Ubr5
|
UTSW |
15 |
37,997,983 (GRCm39) |
missense |
probably benign |
0.02 |
R3900:Ubr5
|
UTSW |
15 |
38,019,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R4032:Ubr5
|
UTSW |
15 |
38,025,081 (GRCm39) |
missense |
|
|
R4352:Ubr5
|
UTSW |
15 |
38,041,817 (GRCm39) |
missense |
probably benign |
0.31 |
R4362:Ubr5
|
UTSW |
15 |
38,078,647 (GRCm39) |
missense |
probably damaging |
0.99 |
R4467:Ubr5
|
UTSW |
15 |
38,004,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R4507:Ubr5
|
UTSW |
15 |
38,013,786 (GRCm39) |
missense |
probably damaging |
0.96 |
R4683:Ubr5
|
UTSW |
15 |
38,038,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Ubr5
|
UTSW |
15 |
38,018,541 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4878:Ubr5
|
UTSW |
15 |
38,006,808 (GRCm39) |
missense |
probably benign |
0.01 |
R4999:Ubr5
|
UTSW |
15 |
38,009,912 (GRCm39) |
missense |
probably benign |
0.06 |
R5057:Ubr5
|
UTSW |
15 |
38,004,353 (GRCm39) |
missense |
probably damaging |
0.98 |
R5177:Ubr5
|
UTSW |
15 |
38,006,761 (GRCm39) |
missense |
probably benign |
0.22 |
R5186:Ubr5
|
UTSW |
15 |
37,998,160 (GRCm39) |
missense |
probably damaging |
0.99 |
R5378:Ubr5
|
UTSW |
15 |
37,989,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R5486:Ubr5
|
UTSW |
15 |
38,008,983 (GRCm39) |
missense |
probably benign |
0.00 |
R5494:Ubr5
|
UTSW |
15 |
38,019,525 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5617:Ubr5
|
UTSW |
15 |
38,030,901 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5636:Ubr5
|
UTSW |
15 |
37,984,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Ubr5
|
UTSW |
15 |
38,015,337 (GRCm39) |
missense |
probably damaging |
0.99 |
R5715:Ubr5
|
UTSW |
15 |
38,002,477 (GRCm39) |
missense |
probably benign |
0.06 |
R5781:Ubr5
|
UTSW |
15 |
38,006,785 (GRCm39) |
missense |
probably benign |
0.27 |
R6645:Ubr5
|
UTSW |
15 |
38,029,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R6774:Ubr5
|
UTSW |
15 |
38,015,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R6823:Ubr5
|
UTSW |
15 |
37,989,842 (GRCm39) |
missense |
probably benign |
0.08 |
R6877:Ubr5
|
UTSW |
15 |
38,002,814 (GRCm39) |
missense |
probably damaging |
0.98 |
R7105:Ubr5
|
UTSW |
15 |
38,009,019 (GRCm39) |
missense |
|
|
R7166:Ubr5
|
UTSW |
15 |
37,976,389 (GRCm39) |
missense |
|
|
R7514:Ubr5
|
UTSW |
15 |
37,988,481 (GRCm39) |
missense |
|
|
R7523:Ubr5
|
UTSW |
15 |
38,004,299 (GRCm39) |
missense |
|
|
R7631:Ubr5
|
UTSW |
15 |
38,029,751 (GRCm39) |
missense |
|
|
R7709:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7710:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7712:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7803:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7816:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7817:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7821:Ubr5
|
UTSW |
15 |
37,997,431 (GRCm39) |
missense |
probably damaging |
0.96 |
R7824:Ubr5
|
UTSW |
15 |
37,991,566 (GRCm39) |
missense |
probably damaging |
0.97 |
R7841:Ubr5
|
UTSW |
15 |
37,981,150 (GRCm39) |
missense |
|
|
R7869:Ubr5
|
UTSW |
15 |
37,980,076 (GRCm39) |
missense |
probably null |
|
R7896:Ubr5
|
UTSW |
15 |
38,041,817 (GRCm39) |
missense |
probably benign |
0.31 |
R8191:Ubr5
|
UTSW |
15 |
38,006,751 (GRCm39) |
missense |
|
|
R8342:Ubr5
|
UTSW |
15 |
38,025,081 (GRCm39) |
missense |
|
|
R8745:Ubr5
|
UTSW |
15 |
38,025,039 (GRCm39) |
missense |
|
|
R8811:Ubr5
|
UTSW |
15 |
38,041,123 (GRCm39) |
missense |
|
|
R8904:Ubr5
|
UTSW |
15 |
38,042,153 (GRCm39) |
missense |
|
|
R8955:Ubr5
|
UTSW |
15 |
38,029,825 (GRCm39) |
missense |
|
|
R8956:Ubr5
|
UTSW |
15 |
38,015,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R9051:Ubr5
|
UTSW |
15 |
38,002,503 (GRCm39) |
missense |
|
|
R9102:Ubr5
|
UTSW |
15 |
38,018,596 (GRCm39) |
missense |
|
|
R9183:Ubr5
|
UTSW |
15 |
37,997,420 (GRCm39) |
missense |
|
|
R9235:Ubr5
|
UTSW |
15 |
38,045,982 (GRCm39) |
missense |
|
|
R9392:Ubr5
|
UTSW |
15 |
37,984,251 (GRCm39) |
missense |
|
|
R9473:Ubr5
|
UTSW |
15 |
38,002,617 (GRCm39) |
missense |
|
|
R9596:Ubr5
|
UTSW |
15 |
37,986,213 (GRCm39) |
missense |
|
|
R9659:Ubr5
|
UTSW |
15 |
37,984,254 (GRCm39) |
missense |
|
|
R9683:Ubr5
|
UTSW |
15 |
37,978,271 (GRCm39) |
missense |
|
|
RF024:Ubr5
|
UTSW |
15 |
38,028,896 (GRCm39) |
missense |
|
|
X0024:Ubr5
|
UTSW |
15 |
37,992,304 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ubr5
|
UTSW |
15 |
38,040,999 (GRCm39) |
missense |
|
|
|