Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
A |
T |
11: 119,902,172 (GRCm39) |
D741E |
probably benign |
Het |
Abca16 |
A |
G |
7: 120,139,351 (GRCm39) |
D1461G |
probably benign |
Het |
Adam6a |
G |
T |
12: 113,509,078 (GRCm39) |
D484Y |
probably damaging |
Het |
Akap5 |
T |
C |
12: 76,376,706 (GRCm39) |
Y713H |
probably damaging |
Het |
AW554918 |
A |
G |
18: 25,473,132 (GRCm39) |
E312G |
possibly damaging |
Het |
Car4 |
G |
A |
11: 84,855,231 (GRCm39) |
A157T |
probably damaging |
Het |
Chst9 |
A |
T |
18: 15,585,849 (GRCm39) |
M238K |
probably benign |
Het |
Ctbp2 |
G |
A |
7: 132,589,974 (GRCm39) |
H397Y |
possibly damaging |
Het |
Cyp3a59 |
A |
G |
5: 146,039,611 (GRCm39) |
M295V |
probably benign |
Het |
Daglb |
T |
C |
5: 143,488,803 (GRCm39) |
Y586H |
probably benign |
Het |
Ehbp1l1 |
G |
T |
19: 5,769,603 (GRCm39) |
P567T |
possibly damaging |
Het |
Emilin2 |
A |
G |
17: 71,580,464 (GRCm39) |
I754T |
probably damaging |
Het |
Esyt2 |
G |
A |
12: 116,329,457 (GRCm39) |
A672T |
probably benign |
Het |
Evx1 |
G |
T |
6: 52,291,175 (GRCm39) |
E116* |
probably null |
Het |
Exph5 |
T |
C |
9: 53,286,278 (GRCm39) |
S1120P |
probably damaging |
Het |
Fam184a |
A |
T |
10: 53,560,450 (GRCm39) |
L515* |
probably null |
Het |
Flt4 |
T |
A |
11: 49,523,996 (GRCm39) |
D525E |
probably benign |
Het |
Galt |
T |
C |
4: 41,756,764 (GRCm39) |
W135R |
probably damaging |
Het |
Ifitm6 |
A |
T |
7: 140,596,648 (GRCm39) |
C42S |
probably damaging |
Het |
Ift172 |
A |
G |
5: 31,442,610 (GRCm39) |
S186P |
probably benign |
Het |
Kcnk3 |
A |
G |
5: 30,779,712 (GRCm39) |
E254G |
probably damaging |
Het |
Ky |
T |
A |
9: 102,414,972 (GRCm39) |
S295T |
probably benign |
Het |
Lrba |
T |
A |
3: 86,571,801 (GRCm39) |
Y2368* |
probably null |
Het |
Mtmr4 |
T |
A |
11: 87,501,953 (GRCm39) |
V669E |
probably benign |
Het |
Myh10 |
C |
T |
11: 68,655,918 (GRCm39) |
R471C |
probably damaging |
Het |
Nav1 |
G |
A |
1: 135,380,671 (GRCm39) |
T1416I |
unknown |
Het |
Nrip1 |
A |
C |
16: 76,090,157 (GRCm39) |
S467A |
probably damaging |
Het |
Ntrk1 |
T |
A |
3: 87,695,941 (GRCm39) |
N190Y |
probably damaging |
Het |
Or14a256 |
A |
T |
7: 86,265,763 (GRCm39) |
L30Q |
probably null |
Het |
Or5h25 |
A |
C |
16: 58,930,964 (GRCm39) |
M3R |
probably benign |
Het |
Pdxp |
A |
G |
15: 78,802,611 (GRCm39) |
S282G |
probably damaging |
Het |
Phtf2 |
A |
T |
5: 21,006,904 (GRCm39) |
S220T |
probably damaging |
Het |
Piezo2 |
A |
T |
18: 63,157,540 (GRCm39) |
V2390E |
probably damaging |
Het |
Pop1 |
T |
G |
15: 34,529,229 (GRCm39) |
L783R |
probably benign |
Het |
Prf1 |
G |
A |
10: 61,135,972 (GRCm39) |
A83T |
probably benign |
Het |
Rab4b |
A |
G |
7: 26,875,267 (GRCm39) |
V50A |
probably benign |
Het |
Rtn1 |
T |
A |
12: 72,351,100 (GRCm39) |
T370S |
probably benign |
Het |
Sdr16c5 |
T |
A |
4: 4,012,423 (GRCm39) |
I123F |
probably damaging |
Het |
Smg6 |
T |
A |
11: 75,046,991 (GRCm39) |
V1228D |
probably damaging |
Het |
Smim19 |
A |
G |
8: 22,963,539 (GRCm39) |
V23A |
probably benign |
Het |
Sox13 |
A |
T |
1: 133,313,996 (GRCm39) |
I346N |
probably damaging |
Het |
Tap1 |
T |
A |
17: 34,412,165 (GRCm39) |
Y457N |
probably damaging |
Het |
Tbck |
C |
T |
3: 132,458,427 (GRCm39) |
P686S |
probably damaging |
Het |
Tcof1 |
A |
G |
18: 60,965,010 (GRCm39) |
S570P |
unknown |
Het |
Tmc5 |
A |
T |
7: 118,271,449 (GRCm39) |
M921L |
probably benign |
Het |
Ttc6 |
A |
G |
12: 57,772,462 (GRCm39) |
Y1594C |
possibly damaging |
Het |
Virma |
T |
A |
4: 11,546,008 (GRCm39) |
H1615Q |
probably damaging |
Het |
Vmn1r19 |
T |
A |
6: 57,382,037 (GRCm39) |
Y197N |
probably damaging |
Het |
Vps13c |
T |
C |
9: 67,845,068 (GRCm39) |
F2051L |
probably damaging |
Het |
Wdr6 |
C |
T |
9: 108,451,765 (GRCm39) |
C706Y |
probably damaging |
Het |
Zfand4 |
A |
G |
6: 116,261,736 (GRCm39) |
N100D |
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 |
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 |
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 |
|
|