Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
G |
13: 77,471,685 (GRCm39) |
N1030S |
possibly damaging |
Het |
4930507D05Rik |
A |
G |
10: 62,285,303 (GRCm39) |
H9R |
unknown |
Het |
Anks1b |
T |
A |
10: 90,802,880 (GRCm39) |
S398T |
probably benign |
Het |
Bbox1 |
T |
A |
2: 110,122,871 (GRCm39) |
K139N |
probably benign |
Het |
Birc6 |
C |
A |
17: 74,948,666 (GRCm39) |
H3047N |
probably damaging |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Camta1 |
G |
A |
4: 151,920,333 (GRCm39) |
S18F |
probably damaging |
Het |
Ccnb1ip1 |
T |
C |
14: 51,031,277 (GRCm39) |
Y12C |
possibly damaging |
Het |
Celsr3 |
G |
A |
9: 108,705,271 (GRCm39) |
A585T |
probably benign |
Het |
Col6a4 |
T |
C |
9: 105,957,497 (GRCm39) |
N109S |
probably benign |
Het |
Crisp4 |
A |
T |
1: 18,198,893 (GRCm39) |
D180E |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 49,997,450 (GRCm39) |
M546K |
probably damaging |
Het |
Dnah11 |
C |
T |
12: 117,951,237 (GRCm39) |
V3024I |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,322,064 (GRCm39) |
D3752G |
probably damaging |
Het |
Dram1 |
G |
T |
10: 88,160,609 (GRCm39) |
D237E |
probably benign |
Het |
Ehbp1l1 |
T |
C |
19: 5,769,426 (GRCm39) |
N626D |
probably benign |
Het |
Elavl1 |
T |
G |
8: 4,361,763 (GRCm39) |
N3T |
probably damaging |
Het |
Fam184a |
A |
G |
10: 53,574,589 (GRCm39) |
V340A |
probably benign |
Het |
Fer1l5 |
C |
T |
1: 36,446,117 (GRCm39) |
T876M |
not run |
Het |
Foxp2 |
T |
A |
6: 15,409,888 (GRCm39) |
V471E |
unknown |
Het |
Fstl5 |
G |
A |
3: 76,443,605 (GRCm39) |
G317R |
probably damaging |
Het |
Gm32742 |
T |
C |
9: 51,060,414 (GRCm39) |
E963G |
possibly damaging |
Het |
Gpbp1 |
A |
T |
13: 111,575,733 (GRCm39) |
S257T |
possibly damaging |
Het |
Gsdmc4 |
C |
T |
15: 63,769,568 (GRCm39) |
C218Y |
possibly damaging |
Het |
Hmg20b |
T |
C |
10: 81,182,442 (GRCm39) |
H298R |
probably damaging |
Het |
Igf2r |
A |
T |
17: 12,967,591 (GRCm39) |
C72S |
probably benign |
Het |
Kcnip1 |
A |
G |
11: 33,583,206 (GRCm39) |
M193T |
probably damaging |
Het |
Khdc1c |
G |
T |
1: 21,439,899 (GRCm39) |
C150F |
probably benign |
Het |
Lnpep |
A |
G |
17: 17,787,001 (GRCm39) |
S533P |
probably benign |
Het |
Megf8 |
T |
A |
7: 25,040,060 (GRCm39) |
V997E |
possibly damaging |
Het |
Mob2 |
T |
C |
7: 141,563,177 (GRCm39) |
Y94C |
probably damaging |
Het |
Muc5ac |
G |
C |
7: 141,363,040 (GRCm39) |
G2117A |
unknown |
Het |
Npepl1 |
A |
G |
2: 173,962,387 (GRCm39) |
D351G |
probably damaging |
Het |
Nrg1 |
G |
A |
8: 32,328,352 (GRCm39) |
Q213* |
probably null |
Het |
Nrp2 |
A |
G |
1: 62,810,990 (GRCm39) |
D677G |
probably benign |
Het |
Or11h7 |
A |
G |
14: 50,890,904 (GRCm39) |
E70G |
probably damaging |
Het |
Or2b4 |
G |
T |
17: 38,116,320 (GRCm39) |
G95C |
probably damaging |
Het |
Or56a3 |
G |
T |
7: 104,735,780 (GRCm39) |
V286F |
probably damaging |
Het |
Or5aq7 |
G |
T |
2: 86,938,401 (GRCm39) |
T110K |
probably damaging |
Het |
Or5m3b |
C |
A |
2: 85,871,814 (GRCm39) |
Q52K |
probably benign |
Het |
Or8c8 |
T |
A |
9: 38,165,406 (GRCm39) |
M228K |
probably benign |
Het |
Peg10 |
ACATCAGGATCC |
ACATCAGGATCCCCATCAGGATCC |
6: 4,756,454 (GRCm39) |
|
probably benign |
Het |
Phaf1 |
C |
A |
8: 105,976,084 (GRCm39) |
T347N |
probably benign |
Het |
Prune2 |
G |
A |
19: 17,100,393 (GRCm39) |
V1966I |
possibly damaging |
Het |
Ptch2 |
A |
G |
4: 116,967,585 (GRCm39) |
H751R |
probably benign |
Het |
Ptges2 |
T |
A |
2: 32,292,243 (GRCm39) |
M353K |
probably damaging |
Het |
Pum3 |
G |
A |
19: 27,373,728 (GRCm39) |
Q564* |
probably null |
Het |
Qtrt1 |
A |
G |
9: 21,330,637 (GRCm39) |
D279G |
probably damaging |
Het |
Rftn1 |
C |
T |
17: 50,354,463 (GRCm39) |
V300I |
probably benign |
Het |
Robo2 |
T |
C |
16: 73,717,585 (GRCm39) |
T1172A |
probably benign |
Het |
Sdc3 |
A |
G |
4: 130,544,244 (GRCm39) |
D74G |
unknown |
Het |
Setd1b |
A |
G |
5: 123,290,336 (GRCm39) |
M768V |
unknown |
Het |
Shld2 |
A |
T |
14: 33,989,724 (GRCm39) |
M394K |
possibly damaging |
Het |
Siglech |
A |
T |
7: 55,422,289 (GRCm39) |
H298L |
probably benign |
Het |
Sipa1 |
A |
T |
19: 5,701,704 (GRCm39) |
L977Q |
probably damaging |
Het |
Slc9c1 |
G |
A |
16: 45,403,332 (GRCm39) |
V800I |
probably benign |
Het |
Spata31e1 |
A |
G |
13: 49,943,547 (GRCm39) |
S44P |
possibly damaging |
Het |
Spata31f1a |
C |
T |
4: 42,851,586 (GRCm39) |
C190Y |
probably benign |
Het |
Tbc1d8 |
C |
T |
1: 39,425,104 (GRCm39) |
R582Q |
probably damaging |
Het |
Tmem247 |
T |
A |
17: 87,229,728 (GRCm39) |
F190I |
probably damaging |
Het |
Trim42 |
C |
A |
9: 97,245,070 (GRCm39) |
A577S |
possibly damaging |
Het |
Ubiad1 |
G |
A |
4: 148,528,726 (GRCm39) |
T61I |
probably benign |
Het |
Usp40 |
G |
A |
1: 87,923,435 (GRCm39) |
Q279* |
probably null |
Het |
Usp48 |
A |
G |
4: 137,360,766 (GRCm39) |
N733S |
probably benign |
Het |
Vmn2r83 |
A |
T |
10: 79,314,261 (GRCm39) |
I170F |
probably benign |
Het |
Xkr4 |
G |
A |
1: 3,286,487 (GRCm39) |
P568S |
probably damaging |
Het |
Zc3h7b |
T |
C |
15: 81,664,679 (GRCm39) |
W513R |
probably damaging |
Het |
Zfp40 |
T |
C |
17: 23,410,440 (GRCm39) |
|
probably benign |
Het |
Zfp652 |
T |
A |
11: 95,640,935 (GRCm39) |
S287T |
possibly damaging |
Het |
Znrf3 |
G |
A |
11: 5,394,533 (GRCm39) |
A49V |
unknown |
Het |
|
Other mutations in Kmt2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00580:Kmt2b
|
APN |
7 |
30,285,938 (GRCm39) |
unclassified |
probably benign |
|
IGL00821:Kmt2b
|
APN |
7 |
30,270,038 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00985:Kmt2b
|
APN |
7 |
30,279,352 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01092:Kmt2b
|
APN |
7 |
30,279,932 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01933:Kmt2b
|
APN |
7 |
30,268,939 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01949:Kmt2b
|
APN |
7 |
30,276,586 (GRCm39) |
splice site |
probably null |
|
IGL02253:Kmt2b
|
APN |
7 |
30,281,152 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02455:Kmt2b
|
APN |
7 |
30,278,303 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02493:Kmt2b
|
APN |
7 |
30,268,936 (GRCm39) |
unclassified |
probably benign |
|
IGL02504:Kmt2b
|
APN |
7 |
30,285,968 (GRCm39) |
unclassified |
probably benign |
|
IGL02532:Kmt2b
|
APN |
7 |
30,286,314 (GRCm39) |
unclassified |
probably benign |
|
IGL02698:Kmt2b
|
APN |
7 |
30,278,118 (GRCm39) |
splice site |
probably benign |
|
IGL02717:Kmt2b
|
APN |
7 |
30,282,869 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02826:Kmt2b
|
APN |
7 |
30,276,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02966:Kmt2b
|
APN |
7 |
30,274,887 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03386:Kmt2b
|
APN |
7 |
30,273,396 (GRCm39) |
missense |
possibly damaging |
0.94 |
Dean
|
UTSW |
7 |
30,268,835 (GRCm39) |
missense |
possibly damaging |
0.83 |
provost
|
UTSW |
7 |
30,281,633 (GRCm39) |
missense |
probably damaging |
1.00 |
tenure
|
UTSW |
7 |
30,268,600 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Kmt2b
|
UTSW |
7 |
30,269,040 (GRCm39) |
nonsense |
probably null |
|
FR4304:Kmt2b
|
UTSW |
7 |
30,285,788 (GRCm39) |
unclassified |
probably benign |
|
FR4340:Kmt2b
|
UTSW |
7 |
30,285,800 (GRCm39) |
unclassified |
probably benign |
|
FR4340:Kmt2b
|
UTSW |
7 |
30,285,794 (GRCm39) |
unclassified |
probably benign |
|
FR4340:Kmt2b
|
UTSW |
7 |
30,285,788 (GRCm39) |
unclassified |
probably benign |
|
FR4342:Kmt2b
|
UTSW |
7 |
30,285,800 (GRCm39) |
unclassified |
probably benign |
|
FR4449:Kmt2b
|
UTSW |
7 |
30,285,794 (GRCm39) |
unclassified |
probably benign |
|
FR4449:Kmt2b
|
UTSW |
7 |
30,285,791 (GRCm39) |
unclassified |
probably benign |
|
FR4449:Kmt2b
|
UTSW |
7 |
30,285,786 (GRCm39) |
unclassified |
probably benign |
|
FR4548:Kmt2b
|
UTSW |
7 |
30,285,805 (GRCm39) |
unclassified |
probably benign |
|
FR4589:Kmt2b
|
UTSW |
7 |
30,285,806 (GRCm39) |
unclassified |
probably benign |
|
FR4589:Kmt2b
|
UTSW |
7 |
30,285,789 (GRCm39) |
nonsense |
probably null |
|
FR4589:Kmt2b
|
UTSW |
7 |
30,285,786 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Kmt2b
|
UTSW |
7 |
30,285,795 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Kmt2b
|
UTSW |
7 |
30,285,792 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Kmt2b
|
UTSW |
7 |
30,285,791 (GRCm39) |
unclassified |
probably benign |
|
FR4737:Kmt2b
|
UTSW |
7 |
30,285,803 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Kmt2b
|
UTSW |
7 |
30,285,787 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Kmt2b
|
UTSW |
7 |
30,285,785 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Kmt2b
|
UTSW |
7 |
30,285,798 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Kmt2b
|
UTSW |
7 |
30,285,791 (GRCm39) |
unclassified |
probably benign |
|
FR4976:Kmt2b
|
UTSW |
7 |
30,285,789 (GRCm39) |
nonsense |
probably null |
|
PIT4403001:Kmt2b
|
UTSW |
7 |
30,285,114 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4802001:Kmt2b
|
UTSW |
7 |
30,278,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R0057:Kmt2b
|
UTSW |
7 |
30,276,217 (GRCm39) |
splice site |
probably benign |
|
R0131:Kmt2b
|
UTSW |
7 |
30,283,346 (GRCm39) |
missense |
probably damaging |
0.99 |
R0241:Kmt2b
|
UTSW |
7 |
30,276,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Kmt2b
|
UTSW |
7 |
30,276,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R0377:Kmt2b
|
UTSW |
7 |
30,273,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Kmt2b
|
UTSW |
7 |
30,276,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R1241:Kmt2b
|
UTSW |
7 |
30,274,365 (GRCm39) |
missense |
probably damaging |
0.98 |
R1252:Kmt2b
|
UTSW |
7 |
30,279,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R1418:Kmt2b
|
UTSW |
7 |
30,276,385 (GRCm39) |
splice site |
probably benign |
|
R1599:Kmt2b
|
UTSW |
7 |
30,270,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R1632:Kmt2b
|
UTSW |
7 |
30,283,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R1745:Kmt2b
|
UTSW |
7 |
30,285,275 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1867:Kmt2b
|
UTSW |
7 |
30,274,083 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1955:Kmt2b
|
UTSW |
7 |
30,274,776 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2040:Kmt2b
|
UTSW |
7 |
30,268,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R2113:Kmt2b
|
UTSW |
7 |
30,282,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R2216:Kmt2b
|
UTSW |
7 |
30,273,490 (GRCm39) |
missense |
probably benign |
0.25 |
R2401:Kmt2b
|
UTSW |
7 |
30,276,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R2518:Kmt2b
|
UTSW |
7 |
30,275,493 (GRCm39) |
missense |
probably benign |
0.10 |
R3436:Kmt2b
|
UTSW |
7 |
30,276,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R4248:Kmt2b
|
UTSW |
7 |
30,273,489 (GRCm39) |
missense |
probably benign |
0.25 |
R4259:Kmt2b
|
UTSW |
7 |
30,280,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R4290:Kmt2b
|
UTSW |
7 |
30,281,261 (GRCm39) |
critical splice donor site |
probably null |
|
R4388:Kmt2b
|
UTSW |
7 |
30,288,015 (GRCm39) |
unclassified |
probably benign |
|
R4542:Kmt2b
|
UTSW |
7 |
30,279,684 (GRCm39) |
missense |
probably damaging |
0.99 |
R4649:Kmt2b
|
UTSW |
7 |
30,285,783 (GRCm39) |
unclassified |
probably benign |
|
R4722:Kmt2b
|
UTSW |
7 |
30,282,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R4891:Kmt2b
|
UTSW |
7 |
30,276,186 (GRCm39) |
nonsense |
probably null |
|
R4916:Kmt2b
|
UTSW |
7 |
30,277,942 (GRCm39) |
missense |
probably damaging |
0.99 |
R5104:Kmt2b
|
UTSW |
7 |
30,269,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R5254:Kmt2b
|
UTSW |
7 |
30,268,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R5262:Kmt2b
|
UTSW |
7 |
30,269,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Kmt2b
|
UTSW |
7 |
30,281,098 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5526:Kmt2b
|
UTSW |
7 |
30,279,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R5609:Kmt2b
|
UTSW |
7 |
30,276,570 (GRCm39) |
missense |
probably damaging |
0.99 |
R6150:Kmt2b
|
UTSW |
7 |
30,287,902 (GRCm39) |
unclassified |
probably benign |
|
R6727:Kmt2b
|
UTSW |
7 |
30,283,984 (GRCm39) |
missense |
probably damaging |
0.98 |
R6824:Kmt2b
|
UTSW |
7 |
30,285,701 (GRCm39) |
unclassified |
probably benign |
|
R7048:Kmt2b
|
UTSW |
7 |
30,268,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R7155:Kmt2b
|
UTSW |
7 |
30,279,388 (GRCm39) |
missense |
probably damaging |
0.99 |
R7307:Kmt2b
|
UTSW |
7 |
30,279,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R7388:Kmt2b
|
UTSW |
7 |
30,281,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R7555:Kmt2b
|
UTSW |
7 |
30,268,835 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7569:Kmt2b
|
UTSW |
7 |
30,268,978 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7616:Kmt2b
|
UTSW |
7 |
30,281,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R7669:Kmt2b
|
UTSW |
7 |
30,282,656 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7999:Kmt2b
|
UTSW |
7 |
30,276,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R8003:Kmt2b
|
UTSW |
7 |
30,268,802 (GRCm39) |
missense |
probably damaging |
0.98 |
R8189:Kmt2b
|
UTSW |
7 |
30,268,756 (GRCm39) |
missense |
probably damaging |
0.98 |
R8291:Kmt2b
|
UTSW |
7 |
30,284,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R8314:Kmt2b
|
UTSW |
7 |
30,278,347 (GRCm39) |
missense |
probably damaging |
0.99 |
R8802:Kmt2b
|
UTSW |
7 |
30,283,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R8954:Kmt2b
|
UTSW |
7 |
30,273,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R9046:Kmt2b
|
UTSW |
7 |
30,285,479 (GRCm39) |
missense |
probably benign |
0.00 |
R9225:Kmt2b
|
UTSW |
7 |
30,286,172 (GRCm39) |
missense |
unknown |
|
R9258:Kmt2b
|
UTSW |
7 |
30,281,893 (GRCm39) |
missense |
probably null |
0.99 |
R9414:Kmt2b
|
UTSW |
7 |
30,282,307 (GRCm39) |
missense |
probably damaging |
0.99 |
R9468:Kmt2b
|
UTSW |
7 |
30,284,513 (GRCm39) |
missense |
probably damaging |
0.98 |
R9508:Kmt2b
|
UTSW |
7 |
30,269,259 (GRCm39) |
missense |
probably damaging |
0.99 |
R9642:Kmt2b
|
UTSW |
7 |
30,283,340 (GRCm39) |
critical splice donor site |
probably null |
|
R9667:Kmt2b
|
UTSW |
7 |
30,287,784 (GRCm39) |
missense |
unknown |
|
R9709:Kmt2b
|
UTSW |
7 |
30,279,228 (GRCm39) |
missense |
probably damaging |
0.98 |
RF001:Kmt2b
|
UTSW |
7 |
30,285,807 (GRCm39) |
unclassified |
probably benign |
|
RF006:Kmt2b
|
UTSW |
7 |
30,285,802 (GRCm39) |
unclassified |
probably benign |
|
RF020:Kmt2b
|
UTSW |
7 |
30,285,807 (GRCm39) |
unclassified |
probably benign |
|
RF021:Kmt2b
|
UTSW |
7 |
30,285,782 (GRCm39) |
unclassified |
probably benign |
|
RF030:Kmt2b
|
UTSW |
7 |
30,285,802 (GRCm39) |
unclassified |
probably benign |
|
RF035:Kmt2b
|
UTSW |
7 |
30,285,782 (GRCm39) |
unclassified |
probably benign |
|
X0067:Kmt2b
|
UTSW |
7 |
30,278,998 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Kmt2b
|
UTSW |
7 |
30,284,676 (GRCm39) |
missense |
probably benign |
0.28 |
Z1176:Kmt2b
|
UTSW |
7 |
30,276,795 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Kmt2b
|
UTSW |
7 |
30,285,841 (GRCm39) |
missense |
unknown |
|
Z1177:Kmt2b
|
UTSW |
7 |
30,283,588 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Kmt2b
|
UTSW |
7 |
30,274,449 (GRCm39) |
missense |
probably benign |
0.08 |
Z1186:Kmt2b
|
UTSW |
7 |
30,284,732 (GRCm39) |
missense |
probably benign |
|
Z1186:Kmt2b
|
UTSW |
7 |
30,274,404 (GRCm39) |
missense |
probably benign |
|
|