Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arc |
C |
A |
15: 74,544,098 (GRCm39) |
V42L |
possibly damaging |
Het |
Clip1 |
C |
T |
5: 123,779,848 (GRCm39) |
E433K |
probably damaging |
Het |
Cmya5 |
T |
C |
13: 93,225,723 (GRCm39) |
T3122A |
probably damaging |
Het |
Ctf2 |
G |
T |
7: 127,318,603 (GRCm39) |
A92E |
probably damaging |
Het |
Ctsw |
G |
T |
19: 5,516,322 (GRCm39) |
R184S |
possibly damaging |
Het |
D130043K22Rik |
A |
G |
13: 25,061,918 (GRCm39) |
E629G |
probably damaging |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Fanci |
T |
C |
7: 79,090,446 (GRCm39) |
I982T |
probably benign |
Het |
Fnbp1 |
T |
C |
2: 30,986,139 (GRCm39) |
D3G |
probably damaging |
Het |
Gm10770 |
G |
A |
2: 150,020,830 (GRCm39) |
T229I |
probably benign |
Het |
Gm35315 |
G |
A |
5: 110,226,578 (GRCm39) |
T287I |
probably benign |
Het |
Itgb3 |
T |
A |
11: 104,524,318 (GRCm39) |
D151E |
probably damaging |
Het |
Lcn8 |
A |
T |
2: 25,544,990 (GRCm39) |
|
probably null |
Het |
Ninl |
A |
G |
2: 150,808,098 (GRCm39) |
L310P |
probably damaging |
Het |
Nop2 |
A |
G |
6: 125,114,274 (GRCm39) |
D215G |
probably benign |
Het |
Or4d10c |
T |
C |
19: 12,065,299 (GRCm39) |
T286A |
probably benign |
Het |
Or6c3 |
A |
G |
10: 129,308,773 (GRCm39) |
T71A |
probably damaging |
Het |
Parg |
T |
C |
14: 31,993,634 (GRCm39) |
W289R |
probably damaging |
Het |
Pdcd4 |
A |
G |
19: 53,915,362 (GRCm39) |
|
probably null |
Het |
Plk2 |
G |
T |
13: 110,532,570 (GRCm39) |
E95* |
probably null |
Het |
Pold1 |
G |
A |
7: 44,188,202 (GRCm39) |
R559C |
probably damaging |
Het |
Ptprc |
T |
C |
1: 138,011,377 (GRCm39) |
D560G |
possibly damaging |
Het |
Rasal3 |
T |
C |
17: 32,616,478 (GRCm39) |
Y290C |
probably damaging |
Het |
Rcsd1 |
T |
A |
1: 165,485,184 (GRCm39) |
S90C |
probably damaging |
Het |
Rttn |
T |
C |
18: 89,128,853 (GRCm39) |
L1935P |
probably damaging |
Het |
Smc1b |
C |
T |
15: 84,976,232 (GRCm39) |
R825Q |
probably benign |
Het |
Srsf11 |
C |
T |
3: 157,728,981 (GRCm39) |
|
probably benign |
Homo |
Tmc3 |
T |
C |
7: 83,247,695 (GRCm39) |
Y230H |
probably damaging |
Het |
Tnfrsf25 |
A |
T |
4: 152,204,084 (GRCm39) |
|
probably null |
Het |
Ubl7 |
T |
C |
9: 57,827,793 (GRCm39) |
L160P |
probably damaging |
Het |
Vmn2r106 |
C |
T |
17: 20,488,725 (GRCm39) |
C558Y |
probably damaging |
Het |
Zfp646 |
T |
A |
7: 127,479,113 (GRCm39) |
V430E |
probably benign |
Het |
|
Other mutations in Dmbt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Dmbt1
|
APN |
7 |
130,681,270 (GRCm39) |
intron |
probably benign |
|
IGL00161:Dmbt1
|
APN |
7 |
130,711,357 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00331:Dmbt1
|
APN |
7 |
130,701,020 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL00769:Dmbt1
|
APN |
7 |
130,684,230 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00792:Dmbt1
|
APN |
7 |
130,699,337 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL00823:Dmbt1
|
APN |
7 |
130,659,888 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01072:Dmbt1
|
APN |
7 |
130,687,098 (GRCm39) |
splice site |
probably benign |
|
IGL01317:Dmbt1
|
APN |
7 |
130,642,921 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01335:Dmbt1
|
APN |
7 |
130,690,497 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01372:Dmbt1
|
APN |
7 |
130,705,409 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01511:Dmbt1
|
APN |
7 |
130,718,457 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01627:Dmbt1
|
APN |
7 |
130,682,915 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01890:Dmbt1
|
APN |
7 |
130,676,149 (GRCm39) |
intron |
probably benign |
|
IGL02160:Dmbt1
|
APN |
7 |
130,684,418 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02186:Dmbt1
|
APN |
7 |
130,694,986 (GRCm39) |
splice site |
probably benign |
|
IGL02197:Dmbt1
|
APN |
7 |
130,687,152 (GRCm39) |
splice site |
probably benign |
|
IGL02332:Dmbt1
|
APN |
7 |
130,668,343 (GRCm39) |
intron |
probably benign |
|
IGL02427:Dmbt1
|
APN |
7 |
130,689,815 (GRCm39) |
splice site |
probably null |
|
IGL02726:Dmbt1
|
APN |
7 |
130,676,140 (GRCm39) |
intron |
probably benign |
|
IGL02967:Dmbt1
|
APN |
7 |
130,672,919 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03003:Dmbt1
|
APN |
7 |
130,684,409 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03089:Dmbt1
|
APN |
7 |
130,712,778 (GRCm39) |
missense |
probably damaging |
0.99 |
cavity
|
UTSW |
7 |
130,713,965 (GRCm39) |
missense |
unknown |
|
lacunar
|
UTSW |
7 |
130,699,361 (GRCm39) |
missense |
probably damaging |
0.97 |
BB005:Dmbt1
|
UTSW |
7 |
130,639,620 (GRCm39) |
missense |
probably benign |
0.16 |
BB015:Dmbt1
|
UTSW |
7 |
130,639,620 (GRCm39) |
missense |
probably benign |
0.16 |
H8562:Dmbt1
|
UTSW |
7 |
130,713,805 (GRCm39) |
nonsense |
probably null |
|
K3955:Dmbt1
|
UTSW |
7 |
130,721,293 (GRCm39) |
missense |
probably damaging |
0.98 |
R0051:Dmbt1
|
UTSW |
7 |
130,721,225 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0051:Dmbt1
|
UTSW |
7 |
130,721,225 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0257:Dmbt1
|
UTSW |
7 |
130,708,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R0388:Dmbt1
|
UTSW |
7 |
130,697,779 (GRCm39) |
splice site |
probably benign |
|
R0427:Dmbt1
|
UTSW |
7 |
130,642,632 (GRCm39) |
nonsense |
probably null |
|
R0478:Dmbt1
|
UTSW |
7 |
130,642,917 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0502:Dmbt1
|
UTSW |
7 |
130,699,403 (GRCm39) |
splice site |
probably null |
|
R0538:Dmbt1
|
UTSW |
7 |
130,651,631 (GRCm39) |
splice site |
probably benign |
|
R0626:Dmbt1
|
UTSW |
7 |
130,703,811 (GRCm39) |
missense |
probably damaging |
0.97 |
R0631:Dmbt1
|
UTSW |
7 |
130,699,383 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0948:Dmbt1
|
UTSW |
7 |
130,694,847 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1169:Dmbt1
|
UTSW |
7 |
130,676,254 (GRCm39) |
critical splice donor site |
probably null |
|
R1413:Dmbt1
|
UTSW |
7 |
130,651,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R1458:Dmbt1
|
UTSW |
7 |
130,646,217 (GRCm39) |
splice site |
probably benign |
|
R1463:Dmbt1
|
UTSW |
7 |
130,711,366 (GRCm39) |
critical splice donor site |
probably null |
|
R1509:Dmbt1
|
UTSW |
7 |
130,676,061 (GRCm39) |
intron |
probably benign |
|
R1990:Dmbt1
|
UTSW |
7 |
130,660,018 (GRCm39) |
missense |
probably damaging |
0.98 |
R2018:Dmbt1
|
UTSW |
7 |
130,712,718 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2019:Dmbt1
|
UTSW |
7 |
130,712,718 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2042:Dmbt1
|
UTSW |
7 |
130,708,089 (GRCm39) |
missense |
probably damaging |
0.99 |
R2056:Dmbt1
|
UTSW |
7 |
130,707,900 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2057:Dmbt1
|
UTSW |
7 |
130,707,900 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2058:Dmbt1
|
UTSW |
7 |
130,707,900 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2059:Dmbt1
|
UTSW |
7 |
130,707,900 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2061:Dmbt1
|
UTSW |
7 |
130,700,863 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2092:Dmbt1
|
UTSW |
7 |
130,651,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R2102:Dmbt1
|
UTSW |
7 |
130,703,762 (GRCm39) |
missense |
probably damaging |
0.97 |
R2155:Dmbt1
|
UTSW |
7 |
130,699,305 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2243:Dmbt1
|
UTSW |
7 |
130,648,292 (GRCm39) |
missense |
probably benign |
0.03 |
R2256:Dmbt1
|
UTSW |
7 |
130,692,224 (GRCm39) |
missense |
probably benign |
0.01 |
R2391:Dmbt1
|
UTSW |
7 |
130,708,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R2394:Dmbt1
|
UTSW |
7 |
130,696,464 (GRCm39) |
nonsense |
probably null |
|
R3014:Dmbt1
|
UTSW |
7 |
130,633,827 (GRCm39) |
intron |
probably benign |
|
R3155:Dmbt1
|
UTSW |
7 |
130,651,887 (GRCm39) |
nonsense |
probably null |
|
R3176:Dmbt1
|
UTSW |
7 |
130,689,801 (GRCm39) |
missense |
probably benign |
0.19 |
R3276:Dmbt1
|
UTSW |
7 |
130,689,801 (GRCm39) |
missense |
probably benign |
0.19 |
R3442:Dmbt1
|
UTSW |
7 |
130,707,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Dmbt1
|
UTSW |
7 |
130,713,819 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4060:Dmbt1
|
UTSW |
7 |
130,675,932 (GRCm39) |
intron |
probably benign |
|
R4396:Dmbt1
|
UTSW |
7 |
130,718,361 (GRCm39) |
missense |
probably damaging |
0.98 |
R4453:Dmbt1
|
UTSW |
7 |
130,642,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R5001:Dmbt1
|
UTSW |
7 |
130,651,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R5051:Dmbt1
|
UTSW |
7 |
130,696,472 (GRCm39) |
missense |
probably benign |
0.01 |
R5156:Dmbt1
|
UTSW |
7 |
130,699,400 (GRCm39) |
critical splice donor site |
probably null |
|
R5225:Dmbt1
|
UTSW |
7 |
130,696,465 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5281:Dmbt1
|
UTSW |
7 |
130,684,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R5308:Dmbt1
|
UTSW |
7 |
130,642,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R5447:Dmbt1
|
UTSW |
7 |
130,721,240 (GRCm39) |
missense |
probably damaging |
0.99 |
R5467:Dmbt1
|
UTSW |
7 |
130,642,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R5497:Dmbt1
|
UTSW |
7 |
130,665,133 (GRCm39) |
intron |
probably benign |
|
R5526:Dmbt1
|
UTSW |
7 |
130,642,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R5554:Dmbt1
|
UTSW |
7 |
130,701,030 (GRCm39) |
nonsense |
probably null |
|
R5566:Dmbt1
|
UTSW |
7 |
130,708,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R5595:Dmbt1
|
UTSW |
7 |
130,655,797 (GRCm39) |
missense |
probably benign |
0.17 |
R6154:Dmbt1
|
UTSW |
7 |
130,711,370 (GRCm39) |
splice site |
probably null |
|
R6188:Dmbt1
|
UTSW |
7 |
130,699,361 (GRCm39) |
missense |
probably damaging |
0.97 |
R6214:Dmbt1
|
UTSW |
7 |
130,668,463 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6215:Dmbt1
|
UTSW |
7 |
130,668,463 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6391:Dmbt1
|
UTSW |
7 |
130,659,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R6397:Dmbt1
|
UTSW |
7 |
130,705,308 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6603:Dmbt1
|
UTSW |
7 |
130,648,240 (GRCm39) |
splice site |
probably null |
|
R6719:Dmbt1
|
UTSW |
7 |
130,721,332 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6781:Dmbt1
|
UTSW |
7 |
130,648,291 (GRCm39) |
missense |
probably benign |
0.16 |
R7148:Dmbt1
|
UTSW |
7 |
130,668,464 (GRCm39) |
nonsense |
probably null |
|
R7191:Dmbt1
|
UTSW |
7 |
130,646,250 (GRCm39) |
missense |
unknown |
|
R7269:Dmbt1
|
UTSW |
7 |
130,668,351 (GRCm39) |
missense |
unknown |
|
R7288:Dmbt1
|
UTSW |
7 |
130,685,519 (GRCm39) |
nonsense |
probably null |
|
R7296:Dmbt1
|
UTSW |
7 |
130,713,861 (GRCm39) |
missense |
unknown |
|
R7349:Dmbt1
|
UTSW |
7 |
130,642,854 (GRCm39) |
missense |
unknown |
|
R7386:Dmbt1
|
UTSW |
7 |
130,713,965 (GRCm39) |
missense |
unknown |
|
R7428:Dmbt1
|
UTSW |
7 |
130,710,192 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7481:Dmbt1
|
UTSW |
7 |
130,681,241 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7486:Dmbt1
|
UTSW |
7 |
130,668,192 (GRCm39) |
missense |
unknown |
|
R7513:Dmbt1
|
UTSW |
7 |
130,692,242 (GRCm39) |
missense |
unknown |
|
R7553:Dmbt1
|
UTSW |
7 |
130,706,597 (GRCm39) |
missense |
unknown |
|
R7567:Dmbt1
|
UTSW |
7 |
130,663,093 (GRCm39) |
splice site |
probably null |
|
R7584:Dmbt1
|
UTSW |
7 |
130,690,481 (GRCm39) |
nonsense |
probably null |
|
R7736:Dmbt1
|
UTSW |
7 |
130,718,625 (GRCm39) |
missense |
unknown |
|
R7758:Dmbt1
|
UTSW |
7 |
130,722,926 (GRCm39) |
missense |
unknown |
|
R7928:Dmbt1
|
UTSW |
7 |
130,639,620 (GRCm39) |
missense |
probably benign |
0.16 |
R8080:Dmbt1
|
UTSW |
7 |
130,690,500 (GRCm39) |
missense |
unknown |
|
R8098:Dmbt1
|
UTSW |
7 |
130,710,188 (GRCm39) |
nonsense |
probably null |
|
R8125:Dmbt1
|
UTSW |
7 |
130,700,953 (GRCm39) |
missense |
unknown |
|
R8177:Dmbt1
|
UTSW |
7 |
130,708,162 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8350:Dmbt1
|
UTSW |
7 |
130,687,147 (GRCm39) |
critical splice donor site |
probably null |
|
R8366:Dmbt1
|
UTSW |
7 |
130,668,330 (GRCm39) |
missense |
unknown |
|
R8378:Dmbt1
|
UTSW |
7 |
130,708,195 (GRCm39) |
missense |
probably damaging |
0.96 |
R8399:Dmbt1
|
UTSW |
7 |
130,684,317 (GRCm39) |
missense |
unknown |
|
R8400:Dmbt1
|
UTSW |
7 |
130,684,317 (GRCm39) |
missense |
unknown |
|
R8445:Dmbt1
|
UTSW |
7 |
130,692,110 (GRCm39) |
missense |
unknown |
|
R8450:Dmbt1
|
UTSW |
7 |
130,687,147 (GRCm39) |
critical splice donor site |
probably null |
|
R8511:Dmbt1
|
UTSW |
7 |
130,703,742 (GRCm39) |
missense |
unknown |
|
R8688:Dmbt1
|
UTSW |
7 |
130,659,984 (GRCm39) |
missense |
unknown |
|
R8850:Dmbt1
|
UTSW |
7 |
130,692,134 (GRCm39) |
missense |
unknown |
|
R8852:Dmbt1
|
UTSW |
7 |
130,642,853 (GRCm39) |
missense |
unknown |
|
R8871:Dmbt1
|
UTSW |
7 |
130,718,597 (GRCm39) |
missense |
unknown |
|
R8943:Dmbt1
|
UTSW |
7 |
130,721,372 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8978:Dmbt1
|
UTSW |
7 |
130,639,611 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9004:Dmbt1
|
UTSW |
7 |
130,713,798 (GRCm39) |
missense |
unknown |
|
R9020:Dmbt1
|
UTSW |
7 |
130,712,787 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9088:Dmbt1
|
UTSW |
7 |
130,718,418 (GRCm39) |
missense |
unknown |
|
R9230:Dmbt1
|
UTSW |
7 |
130,639,642 (GRCm39) |
missense |
probably benign |
0.01 |
R9304:Dmbt1
|
UTSW |
7 |
130,700,855 (GRCm39) |
missense |
unknown |
|
R9377:Dmbt1
|
UTSW |
7 |
130,694,832 (GRCm39) |
missense |
unknown |
|
R9428:Dmbt1
|
UTSW |
7 |
130,668,208 (GRCm39) |
missense |
unknown |
|
R9474:Dmbt1
|
UTSW |
7 |
130,675,987 (GRCm39) |
missense |
unknown |
|
R9573:Dmbt1
|
UTSW |
7 |
130,657,910 (GRCm39) |
critical splice donor site |
probably null |
|
R9675:Dmbt1
|
UTSW |
7 |
130,712,652 (GRCm39) |
missense |
probably damaging |
0.98 |
R9689:Dmbt1
|
UTSW |
7 |
130,660,015 (GRCm39) |
missense |
unknown |
|
R9781:Dmbt1
|
UTSW |
7 |
130,639,599 (GRCm39) |
missense |
probably benign |
0.00 |
X0024:Dmbt1
|
UTSW |
7 |
130,713,977 (GRCm39) |
nonsense |
probably null |
|
X0062:Dmbt1
|
UTSW |
7 |
130,696,581 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1176:Dmbt1
|
UTSW |
7 |
130,690,542 (GRCm39) |
missense |
unknown |
|
Z1177:Dmbt1
|
UTSW |
7 |
130,684,215 (GRCm39) |
critical splice acceptor site |
probably null |
|
|