Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563M21Rik |
A |
G |
9: 55,896,738 (GRCm39) |
F290S |
probably benign |
Het |
4931414P19Rik |
T |
C |
14: 54,823,123 (GRCm39) |
D358G |
probably damaging |
Het |
A630089N07Rik |
T |
A |
16: 97,867,410 (GRCm39) |
Q184L |
probably damaging |
Het |
Adam10 |
A |
G |
9: 70,629,993 (GRCm39) |
R142G |
possibly damaging |
Het |
Adgrb1 |
A |
G |
15: 74,420,418 (GRCm39) |
T856A |
probably damaging |
Het |
Angel1 |
A |
G |
12: 86,764,510 (GRCm39) |
S493P |
probably benign |
Het |
Arid1b |
C |
G |
17: 5,045,661 (GRCm39) |
P150A |
unknown |
Het |
Atp8b5 |
T |
A |
4: 43,370,823 (GRCm39) |
|
probably null |
Het |
Cbfa2t3 |
T |
G |
8: 123,360,076 (GRCm39) |
Q525P |
possibly damaging |
Het |
Clip4 |
T |
C |
17: 72,141,268 (GRCm39) |
Y541H |
probably benign |
Het |
Cracr2a |
C |
T |
6: 127,585,660 (GRCm39) |
Q153* |
probably null |
Het |
Dsp |
G |
T |
13: 38,375,458 (GRCm39) |
C1081F |
probably damaging |
Het |
Dysf |
A |
G |
6: 84,078,945 (GRCm39) |
D708G |
probably benign |
Het |
Eif3d |
A |
T |
15: 77,845,886 (GRCm39) |
D378E |
probably damaging |
Het |
Etv1 |
T |
A |
12: 38,915,605 (GRCm39) |
M424K |
probably damaging |
Het |
Fam120b |
T |
G |
17: 15,623,098 (GRCm39) |
S359A |
possibly damaging |
Het |
Ffar2 |
A |
G |
7: 30,519,357 (GRCm39) |
L61P |
probably damaging |
Het |
Grm5 |
A |
T |
7: 87,765,409 (GRCm39) |
D879V |
probably benign |
Het |
Itpr3 |
C |
A |
17: 27,307,951 (GRCm39) |
A246E |
probably damaging |
Het |
Mamdc2 |
T |
A |
19: 23,328,168 (GRCm39) |
Y400F |
probably damaging |
Het |
Mtcl3 |
T |
C |
10: 29,022,574 (GRCm39) |
|
probably benign |
Het |
Muc4 |
T |
A |
16: 32,574,161 (GRCm39) |
Y746* |
probably null |
Het |
Mylk |
T |
C |
16: 34,699,927 (GRCm39) |
F430S |
probably damaging |
Het |
Nek10 |
G |
A |
14: 14,937,759 (GRCm38) |
C826Y |
probably benign |
Het |
Nf1 |
T |
A |
11: 79,275,092 (GRCm39) |
F51Y |
probably damaging |
Het |
Or10ag55-ps1 |
T |
C |
2: 87,115,617 (GRCm39) |
*328Q |
probably null |
Het |
Phf2 |
T |
A |
13: 48,961,083 (GRCm39) |
Y869F |
unknown |
Het |
Psmb7 |
T |
C |
2: 38,523,976 (GRCm39) |
Y133C |
possibly damaging |
Het |
Ptcd2 |
G |
A |
13: 99,481,207 (GRCm39) |
|
probably benign |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Slbp |
A |
T |
5: 33,801,210 (GRCm39) |
I167N |
probably damaging |
Het |
Slc2a2 |
A |
G |
3: 28,781,260 (GRCm39) |
T433A |
probably benign |
Het |
Snap91 |
T |
A |
9: 86,721,674 (GRCm39) |
N55I |
probably damaging |
Het |
Stat4 |
A |
T |
1: 52,053,037 (GRCm39) |
K73* |
probably null |
Het |
Sult2a5 |
G |
A |
7: 13,404,607 (GRCm39) |
M281I |
probably benign |
Het |
Tenm3 |
A |
T |
8: 48,794,084 (GRCm39) |
M647K |
possibly damaging |
Het |
Trim66 |
T |
A |
7: 109,082,956 (GRCm39) |
D162V |
probably damaging |
Het |
Vangl1 |
A |
T |
3: 102,091,381 (GRCm39) |
I235N |
probably damaging |
Het |
Vmn1r175 |
T |
A |
7: 23,508,031 (GRCm39) |
I199F |
possibly damaging |
Het |
Vmn1r72 |
A |
G |
7: 11,404,272 (GRCm39) |
S59P |
probably damaging |
Het |
Wdr25 |
G |
A |
12: 108,958,819 (GRCm39) |
G344S |
possibly damaging |
Het |
Zfand2a |
A |
T |
5: 139,464,321 (GRCm39) |
N61K |
probably damaging |
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 |
R7669:Kmt2b
|
UTSW |
7 |
30,282,656 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7881:Kmt2b
|
UTSW |
7 |
30,279,208 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
|