Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A030005L19Rik |
GTGGTGGCTG |
GTGGTGGCTGTGGTGGCTG |
1: 82,891,290 (GRCm39) |
|
probably benign |
Het |
AI837181 |
CGG |
CGGTGG |
19: 5,475,262 (GRCm39) |
|
probably benign |
Het |
Ankrd44 |
T |
C |
1: 54,817,471 (GRCm39) |
H79R |
probably damaging |
Het |
Atg9a |
T |
A |
1: 75,159,273 (GRCm39) |
E826V |
probably damaging |
Het |
Atrnl1 |
T |
C |
19: 57,630,905 (GRCm39) |
V224A |
probably benign |
Het |
Bltp1 |
TTATTATTATTAT |
TTATTATTATTATTAATATTATTATTAT |
3: 37,104,897 (GRCm39) |
|
probably benign |
Het |
Cpn2 |
G |
A |
16: 30,078,156 (GRCm39) |
A515V |
probably benign |
Het |
Cyp2a12 |
T |
C |
7: 26,734,785 (GRCm39) |
F402S |
possibly damaging |
Het |
Defb22 |
TGCGGCA |
TGCGGCAGAGCTGGGCGTTGCGGCA |
2: 152,327,752 (GRCm39) |
|
probably benign |
Het |
Dnah10 |
G |
T |
5: 124,854,971 (GRCm39) |
V2016F |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,542,290 (GRCm39) |
|
probably null |
Het |
Efhd2 |
GCC |
GCCGCCCCC |
4: 141,602,084 (GRCm39) |
|
probably benign |
Het |
Fam131a |
A |
C |
16: 20,513,690 (GRCm39) |
|
probably benign |
Het |
Gm7247 |
AGACCAGACC |
A |
14: 51,601,781 (GRCm39) |
|
probably benign |
Het |
Gna13 |
T |
C |
11: 109,283,218 (GRCm39) |
V186A |
probably benign |
Het |
Grk3 |
T |
A |
5: 113,089,554 (GRCm39) |
I333L |
probably benign |
Het |
Gstp1 |
A |
T |
19: 4,085,507 (GRCm39) |
V200E |
probably benign |
Het |
Gtf2h1 |
T |
G |
7: 46,453,289 (GRCm39) |
V74G |
possibly damaging |
Het |
Kcnh8 |
G |
A |
17: 53,285,267 (GRCm39) |
R1079H |
probably benign |
Het |
Kiz |
A |
G |
2: 146,712,750 (GRCm39) |
D138G |
possibly damaging |
Het |
Lats1 |
A |
G |
10: 7,586,372 (GRCm39) |
T912A |
probably damaging |
Het |
Lce1m |
GCTGCCACC |
GCTGCCACCACTTCTGCCACC |
3: 92,925,576 (GRCm39) |
|
probably benign |
Het |
Lce1m |
TGCC |
TGCCGCCGCTGCCGCC |
3: 92,925,602 (GRCm39) |
|
probably benign |
Het |
Lrrc2 |
TTGATTCGGTTCACC |
T |
9: 110,810,744 (GRCm39) |
|
probably null |
Het |
Med12l |
T |
C |
3: 58,980,711 (GRCm39) |
F359S |
probably benign |
Het |
Mmut |
A |
G |
17: 41,262,649 (GRCm39) |
I444V |
probably benign |
Het |
Ncoa2 |
CTTAAAA |
C |
1: 13,219,333 (GRCm39) |
|
probably benign |
Het |
Ngp |
A |
G |
9: 110,250,824 (GRCm39) |
T114A |
possibly damaging |
Het |
Nlrc5 |
A |
T |
8: 95,203,516 (GRCm39) |
T539S |
probably benign |
Het |
Nxf1 |
A |
G |
19: 8,749,673 (GRCm39) |
D190G |
probably damaging |
Het |
Or6c2b |
A |
T |
10: 128,948,211 (GRCm39) |
F28I |
probably damaging |
Het |
Or8g2 |
A |
T |
9: 39,821,341 (GRCm39) |
M81L |
probably benign |
Het |
Pramel16 |
C |
G |
4: 143,675,478 (GRCm39) |
Q449H |
probably damaging |
Het |
Prdm15 |
G |
A |
16: 97,609,956 (GRCm39) |
H563Y |
probably damaging |
Het |
Rbm12 |
CAGG |
CAGGGATTGCGGGACCTGGTATTGCGGGACCAGG |
2: 155,938,026 (GRCm39) |
|
probably benign |
Het |
Sema3g |
C |
T |
14: 30,949,798 (GRCm39) |
H660Y |
probably damaging |
Het |
Slco1a8 |
A |
T |
6: 141,954,440 (GRCm39) |
V31E |
probably damaging |
Het |
Smarca2 |
AGCAGCAGCAGCAGCAGCAGCA |
AGCAGCAGCAGCAGCAGCAGCAGCAGCA |
19: 26,608,397 (GRCm39) |
|
probably benign |
Het |
Stpg2 |
A |
T |
3: 138,918,011 (GRCm39) |
|
probably null |
Het |
Taar7f |
C |
T |
10: 23,926,321 (GRCm39) |
T305M |
possibly damaging |
Het |
Tbcb |
C |
T |
7: 29,923,771 (GRCm39) |
V208M |
probably damaging |
Het |
Tenm2 |
T |
A |
11: 35,915,030 (GRCm39) |
Q2169L |
possibly damaging |
Het |
Tln1 |
A |
G |
4: 43,555,890 (GRCm39) |
V108A |
probably damaging |
Het |
Tmc8 |
T |
C |
11: 117,674,060 (GRCm39) |
M42T |
probably benign |
Het |
Trdc |
T |
C |
14: 54,381,660 (GRCm39) |
V115A |
|
Het |
Ttbk2 |
A |
G |
2: 120,579,115 (GRCm39) |
V669A |
probably benign |
Het |
Tusc1 |
GCC |
GCCACCACC |
4: 93,223,553 (GRCm39) |
|
probably benign |
Het |
Utp25 |
A |
G |
1: 192,802,974 (GRCm39) |
F248L |
probably benign |
Het |
Vps16 |
A |
G |
2: 130,280,129 (GRCm39) |
H118R |
probably benign |
Het |
Wdpcp |
T |
A |
11: 21,661,587 (GRCm39) |
C286* |
probably null |
Het |
Zbed4 |
C |
A |
15: 88,665,439 (GRCm39) |
Y502* |
probably null |
Het |
Zdbf2 |
T |
A |
1: 63,341,811 (GRCm39) |
N63K |
possibly 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 |
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 |
|
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 |
|
|