Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc10 |
A |
T |
17: 46,623,359 (GRCm39) |
V851E |
probably benign |
Het |
Adam28 |
A |
G |
14: 68,870,620 (GRCm39) |
I351T |
probably benign |
Het |
Agrp |
G |
T |
8: 106,293,467 (GRCm39) |
T106K |
probably damaging |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Ap2a1 |
T |
C |
7: 44,556,369 (GRCm39) |
E285G |
probably damaging |
Het |
Arfgef1 |
A |
C |
1: 10,243,480 (GRCm39) |
I1023R |
probably damaging |
Het |
Atp2c2 |
G |
A |
8: 120,451,833 (GRCm39) |
V133I |
probably benign |
Het |
Bpifb6 |
A |
G |
2: 153,753,403 (GRCm39) |
T401A |
possibly damaging |
Het |
Capn3 |
G |
A |
2: 120,320,170 (GRCm39) |
V283M |
possibly damaging |
Het |
Chd6 |
A |
T |
2: 160,823,587 (GRCm39) |
V1261E |
probably damaging |
Het |
Col22a1 |
C |
T |
15: 71,878,636 (GRCm39) |
A174T |
probably damaging |
Het |
Crnn |
T |
C |
3: 93,054,198 (GRCm39) |
V27A |
probably benign |
Het |
Dclk2 |
C |
T |
3: 86,712,946 (GRCm39) |
R503Q |
possibly damaging |
Het |
Dgkd |
T |
C |
1: 87,859,766 (GRCm39) |
|
probably null |
Het |
Diaph3 |
A |
G |
14: 87,203,996 (GRCm39) |
L554P |
probably damaging |
Het |
Ephb4 |
A |
T |
5: 137,358,696 (GRCm39) |
H293L |
probably benign |
Het |
Erbin |
G |
T |
13: 103,975,957 (GRCm39) |
H646N |
probably damaging |
Het |
Faiml |
T |
C |
9: 99,116,511 (GRCm39) |
N60D |
probably benign |
Het |
Fem1al |
A |
G |
11: 29,774,723 (GRCm39) |
S245P |
probably benign |
Het |
Flot1 |
A |
G |
17: 36,135,552 (GRCm39) |
E102G |
probably damaging |
Het |
Fryl |
G |
A |
5: 73,190,204 (GRCm39) |
|
probably benign |
Het |
Gad1-ps |
A |
T |
10: 99,281,386 (GRCm39) |
|
noncoding transcript |
Het |
Gtf3c3 |
A |
G |
1: 54,473,371 (GRCm39) |
S81P |
probably damaging |
Het |
Hs1bp3 |
C |
T |
12: 8,371,690 (GRCm39) |
Q91* |
probably null |
Het |
Igf1r |
T |
C |
7: 67,819,661 (GRCm39) |
C324R |
probably damaging |
Het |
Il23r |
G |
A |
6: 67,443,275 (GRCm39) |
T276I |
probably damaging |
Het |
Ip6k1 |
G |
A |
9: 107,918,195 (GRCm39) |
E77K |
possibly damaging |
Het |
Kctd1 |
A |
T |
18: 15,196,263 (GRCm39) |
|
probably benign |
Het |
Man2b1 |
T |
A |
8: 85,820,563 (GRCm39) |
F617I |
probably damaging |
Het |
Med15 |
G |
A |
16: 17,473,570 (GRCm39) |
|
probably benign |
Het |
Myo9b |
A |
G |
8: 71,806,691 (GRCm39) |
K1543R |
probably damaging |
Het |
N4bp2 |
A |
G |
5: 65,948,165 (GRCm39) |
Y265C |
probably benign |
Het |
N4bp2l2 |
A |
T |
5: 150,585,424 (GRCm39) |
N185K |
probably benign |
Het |
Nkx2-1 |
A |
G |
12: 56,580,529 (GRCm39) |
M137T |
probably benign |
Het |
Or51q1c |
A |
G |
7: 103,653,270 (GRCm39) |
T269A |
probably benign |
Het |
Prickle2 |
A |
T |
6: 92,353,574 (GRCm39) |
Y631N |
probably damaging |
Het |
Ptpro |
A |
G |
6: 137,377,643 (GRCm39) |
T698A |
probably benign |
Het |
Rapgef3 |
T |
C |
15: 97,648,059 (GRCm39) |
I690V |
probably benign |
Het |
Rnf44 |
G |
A |
13: 54,830,005 (GRCm39) |
R271W |
probably damaging |
Het |
Rundc3a |
GAGCC |
GAGCCAGCC |
11: 102,291,739 (GRCm39) |
|
probably null |
Het |
Ryr2 |
A |
G |
13: 11,805,153 (GRCm39) |
Y904H |
probably damaging |
Het |
Suz12 |
T |
C |
11: 79,912,922 (GRCm39) |
L322P |
probably damaging |
Het |
Tnfsf13 |
G |
A |
11: 69,575,973 (GRCm39) |
A38V |
probably benign |
Het |
Topbp1 |
G |
A |
9: 103,186,044 (GRCm39) |
R62H |
probably benign |
Het |
Tor1aip1 |
G |
T |
1: 155,906,180 (GRCm39) |
|
probably null |
Het |
Trpv4 |
A |
T |
5: 114,771,215 (GRCm39) |
V438E |
probably damaging |
Het |
Tsku |
A |
T |
7: 98,001,386 (GRCm39) |
V315E |
possibly damaging |
Het |
Ttc38 |
T |
C |
15: 85,717,373 (GRCm39) |
L16P |
probably damaging |
Het |
Vmn1r170 |
A |
G |
7: 23,305,759 (GRCm39) |
I54V |
probably damaging |
Het |
Vmn1r71 |
T |
C |
7: 10,482,196 (GRCm39) |
D98G |
probably benign |
Het |
Wdfy3 |
A |
T |
5: 102,096,795 (GRCm39) |
D334E |
probably damaging |
Het |
Zfhx3 |
T |
A |
8: 109,682,494 (GRCm39) |
F3311Y |
unknown |
Het |
Zswim9 |
A |
G |
7: 13,003,482 (GRCm39) |
S123P |
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 |
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 |
|
|