Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
A |
T |
6: 23,109,497 (GRCm39) |
D324E |
possibly damaging |
Het |
Adam7 |
T |
C |
14: 68,757,988 (GRCm39) |
T245A |
probably benign |
Het |
Adgrf3 |
G |
A |
5: 30,402,367 (GRCm39) |
Q554* |
probably null |
Het |
Aim2 |
T |
C |
1: 173,287,417 (GRCm39) |
|
probably null |
Het |
Arhgef1 |
G |
T |
7: 24,625,271 (GRCm39) |
D850Y |
probably damaging |
Het |
Aspm |
C |
A |
1: 139,398,493 (GRCm39) |
Q1024K |
probably damaging |
Het |
C7 |
T |
C |
15: 5,019,946 (GRCm39) |
S734G |
probably benign |
Het |
Ccdc158 |
A |
T |
5: 92,771,255 (GRCm39) |
S987T |
probably benign |
Het |
Chrna2 |
C |
A |
14: 66,380,873 (GRCm39) |
Y47* |
probably null |
Het |
Chrna2 |
G |
T |
14: 66,380,866 (GRCm39) |
G45V |
probably benign |
Het |
Clec2g |
C |
A |
6: 128,958,287 (GRCm39) |
Q117K |
probably damaging |
Het |
Cntnap5a |
A |
G |
1: 116,029,304 (GRCm39) |
S253G |
probably benign |
Het |
Cttn |
T |
A |
7: 144,011,461 (GRCm39) |
D116V |
probably damaging |
Het |
Cyp2c40 |
A |
G |
19: 39,790,973 (GRCm39) |
V286A |
probably benign |
Het |
Dcbld2 |
T |
A |
16: 58,285,736 (GRCm39) |
S632T |
probably damaging |
Het |
Dscam |
A |
T |
16: 96,484,972 (GRCm39) |
N1118K |
probably benign |
Het |
Eif2a |
C |
T |
3: 58,447,050 (GRCm39) |
T92M |
possibly damaging |
Het |
Frmpd1 |
T |
A |
4: 45,284,382 (GRCm39) |
C1068S |
probably benign |
Het |
Fstl1 |
G |
A |
16: 37,642,965 (GRCm39) |
V110I |
probably benign |
Het |
Gpat2 |
T |
C |
2: 127,275,542 (GRCm39) |
I465T |
probably damaging |
Het |
Gpr137 |
C |
T |
19: 6,917,791 (GRCm39) |
|
probably benign |
Het |
Hgsnat |
A |
G |
8: 26,436,371 (GRCm39) |
I561T |
probably benign |
Het |
Ift74 |
T |
A |
4: 94,541,149 (GRCm39) |
|
probably null |
Het |
Ilf3 |
A |
G |
9: 21,314,430 (GRCm39) |
|
probably null |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Lrrc41 |
C |
A |
4: 115,937,743 (GRCm39) |
|
probably null |
Het |
Myh11 |
C |
A |
16: 14,041,923 (GRCm39) |
R700L |
possibly damaging |
Het |
Myo16 |
A |
G |
8: 10,612,240 (GRCm39) |
D1295G |
probably damaging |
Het |
Myo5b |
A |
G |
18: 74,873,559 (GRCm39) |
M1488V |
probably benign |
Het |
Naip6 |
A |
T |
13: 100,435,815 (GRCm39) |
Y903N |
probably damaging |
Het |
Nek6 |
A |
G |
2: 38,440,649 (GRCm39) |
H19R |
probably damaging |
Het |
Nktr |
A |
C |
9: 121,570,192 (GRCm39) |
T127P |
probably damaging |
Het |
Noc4l |
A |
T |
5: 110,797,738 (GRCm39) |
D335E |
probably benign |
Het |
Or1ad1 |
G |
A |
11: 50,875,683 (GRCm39) |
D52N |
probably damaging |
Het |
Or5h22 |
A |
T |
16: 58,894,619 (GRCm39) |
F275I |
probably damaging |
Het |
Pabpc2 |
A |
T |
18: 39,908,583 (GRCm39) |
Q616L |
possibly damaging |
Het |
Pcdhga4 |
A |
T |
18: 37,818,832 (GRCm39) |
D127V |
probably damaging |
Het |
Phrf1 |
T |
C |
7: 140,839,633 (GRCm39) |
|
probably benign |
Het |
Phtf2 |
T |
A |
5: 21,018,294 (GRCm39) |
I16F |
probably damaging |
Het |
Plekhg3 |
G |
T |
12: 76,624,755 (GRCm39) |
R1200L |
probably benign |
Het |
Plod3 |
G |
C |
5: 137,017,000 (GRCm39) |
A50P |
probably benign |
Het |
Prorp |
G |
T |
12: 55,351,398 (GRCm39) |
V236F |
possibly damaging |
Het |
Prss12 |
A |
G |
3: 123,279,134 (GRCm39) |
N404D |
probably benign |
Het |
Ptch2 |
C |
G |
4: 116,968,403 (GRCm39) |
A926G |
probably damaging |
Het |
Ptpra |
T |
C |
2: 30,333,317 (GRCm39) |
F6L |
probably damaging |
Het |
Reck |
T |
C |
4: 43,942,293 (GRCm39) |
I853T |
possibly damaging |
Het |
Reep6 |
G |
A |
10: 80,165,996 (GRCm39) |
|
probably benign |
Het |
Rex2 |
T |
A |
4: 147,143,154 (GRCm39) |
S547R |
probably benign |
Het |
Rgs22 |
C |
T |
15: 36,107,222 (GRCm39) |
E55K |
probably damaging |
Het |
Rtl6 |
T |
C |
15: 84,441,202 (GRCm39) |
T65A |
possibly damaging |
Het |
Scarb1 |
G |
T |
5: 125,354,859 (GRCm39) |
P491Q |
probably damaging |
Het |
Scfd1 |
A |
G |
12: 51,478,302 (GRCm39) |
S505G |
probably benign |
Het |
Scube1 |
T |
G |
15: 83,492,948 (GRCm39) |
Q904P |
probably damaging |
Het |
Sis |
T |
C |
3: 72,828,517 (GRCm39) |
Y1186C |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,041,632 (GRCm39) |
D1334G |
probably benign |
Het |
Spty2d1 |
T |
C |
7: 46,648,329 (GRCm39) |
E200G |
probably damaging |
Het |
Stard13 |
C |
A |
5: 151,016,294 (GRCm39) |
|
probably null |
Het |
Sybu |
T |
C |
15: 44,582,339 (GRCm39) |
K95R |
probably damaging |
Het |
Trappc9 |
T |
A |
15: 72,813,796 (GRCm39) |
D488V |
probably damaging |
Het |
Txk |
G |
A |
5: 72,858,006 (GRCm39) |
P381S |
probably damaging |
Het |
Ubr2 |
A |
T |
17: 47,299,648 (GRCm39) |
M198K |
probably benign |
Het |
Unc5a |
A |
T |
13: 55,152,294 (GRCm39) |
T786S |
possibly damaging |
Het |
Unc93b1 |
G |
A |
19: 3,991,959 (GRCm39) |
R231Q |
probably damaging |
Het |
Wfdc1 |
T |
A |
8: 120,410,532 (GRCm39) |
|
probably null |
Het |
Zfp667 |
T |
G |
7: 6,308,105 (GRCm39) |
C258G |
possibly damaging |
Het |
Zfr |
G |
A |
15: 12,162,319 (GRCm39) |
R823H |
probably benign |
Het |
|
Other mutations in Nsd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00777:Nsd1
|
APN |
13 |
55,386,548 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01060:Nsd1
|
APN |
13 |
55,411,242 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01125:Nsd1
|
APN |
13 |
55,393,430 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01746:Nsd1
|
APN |
13 |
55,424,328 (GRCm39) |
splice site |
probably null |
|
IGL02437:Nsd1
|
APN |
13 |
55,461,254 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02530:Nsd1
|
APN |
13 |
55,450,646 (GRCm39) |
splice site |
probably benign |
|
IGL02557:Nsd1
|
APN |
13 |
55,460,261 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02572:Nsd1
|
APN |
13 |
55,443,943 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02665:Nsd1
|
APN |
13 |
55,443,996 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02870:Nsd1
|
APN |
13 |
55,461,416 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03181:Nsd1
|
APN |
13 |
55,394,858 (GRCm39) |
missense |
probably damaging |
1.00 |
Amanuensis
|
UTSW |
13 |
55,409,439 (GRCm39) |
nonsense |
probably null |
|
handwriting
|
UTSW |
13 |
55,461,359 (GRCm39) |
missense |
|
|
Prothonotary
|
UTSW |
13 |
55,430,570 (GRCm39) |
missense |
probably damaging |
1.00 |
scribe
|
UTSW |
13 |
55,439,049 (GRCm39) |
missense |
probably damaging |
1.00 |
stenographer
|
UTSW |
13 |
55,446,189 (GRCm39) |
splice site |
probably null |
|
PIT4480001:Nsd1
|
UTSW |
13 |
55,361,731 (GRCm39) |
missense |
probably benign |
0.11 |
R0316:Nsd1
|
UTSW |
13 |
55,361,584 (GRCm39) |
missense |
probably damaging |
0.98 |
R0519:Nsd1
|
UTSW |
13 |
55,460,648 (GRCm39) |
missense |
probably benign |
0.04 |
R0542:Nsd1
|
UTSW |
13 |
55,408,271 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0563:Nsd1
|
UTSW |
13 |
55,394,391 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0652:Nsd1
|
UTSW |
13 |
55,395,399 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0906:Nsd1
|
UTSW |
13 |
55,425,403 (GRCm39) |
missense |
probably benign |
0.30 |
R1560:Nsd1
|
UTSW |
13 |
55,394,533 (GRCm39) |
nonsense |
probably null |
|
R1572:Nsd1
|
UTSW |
13 |
55,394,782 (GRCm39) |
missense |
probably damaging |
0.98 |
R1693:Nsd1
|
UTSW |
13 |
55,395,074 (GRCm39) |
missense |
probably benign |
|
R1697:Nsd1
|
UTSW |
13 |
55,361,872 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1720:Nsd1
|
UTSW |
13 |
55,394,711 (GRCm39) |
missense |
probably damaging |
0.98 |
R1829:Nsd1
|
UTSW |
13 |
55,394,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1834:Nsd1
|
UTSW |
13 |
55,461,164 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1842:Nsd1
|
UTSW |
13 |
55,394,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R1880:Nsd1
|
UTSW |
13 |
55,361,606 (GRCm39) |
missense |
probably damaging |
0.99 |
R2022:Nsd1
|
UTSW |
13 |
55,361,092 (GRCm39) |
missense |
probably damaging |
0.99 |
R2075:Nsd1
|
UTSW |
13 |
55,458,313 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2143:Nsd1
|
UTSW |
13 |
55,408,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Nsd1
|
UTSW |
13 |
55,439,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R2316:Nsd1
|
UTSW |
13 |
55,381,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R2359:Nsd1
|
UTSW |
13 |
55,361,524 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2361:Nsd1
|
UTSW |
13 |
55,361,524 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2656:Nsd1
|
UTSW |
13 |
55,394,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R2849:Nsd1
|
UTSW |
13 |
55,361,505 (GRCm39) |
missense |
probably damaging |
0.99 |
R3237:Nsd1
|
UTSW |
13 |
55,460,701 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3772:Nsd1
|
UTSW |
13 |
55,394,486 (GRCm39) |
missense |
probably benign |
0.00 |
R3773:Nsd1
|
UTSW |
13 |
55,394,486 (GRCm39) |
missense |
probably benign |
0.00 |
R3849:Nsd1
|
UTSW |
13 |
55,394,504 (GRCm39) |
missense |
probably benign |
0.00 |
R3951:Nsd1
|
UTSW |
13 |
55,416,267 (GRCm39) |
missense |
probably benign |
0.05 |
R4036:Nsd1
|
UTSW |
13 |
55,361,524 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4073:Nsd1
|
UTSW |
13 |
55,395,541 (GRCm39) |
missense |
probably benign |
0.28 |
R4226:Nsd1
|
UTSW |
13 |
55,408,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R4485:Nsd1
|
UTSW |
13 |
55,393,434 (GRCm39) |
missense |
probably benign |
|
R4703:Nsd1
|
UTSW |
13 |
55,361,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R4853:Nsd1
|
UTSW |
13 |
55,416,317 (GRCm39) |
missense |
probably benign |
0.30 |
R4915:Nsd1
|
UTSW |
13 |
55,424,341 (GRCm39) |
missense |
probably benign |
0.00 |
R4915:Nsd1
|
UTSW |
13 |
55,395,681 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5264:Nsd1
|
UTSW |
13 |
55,395,159 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5348:Nsd1
|
UTSW |
13 |
55,460,147 (GRCm39) |
missense |
probably benign |
0.00 |
R5473:Nsd1
|
UTSW |
13 |
55,395,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R5498:Nsd1
|
UTSW |
13 |
55,361,115 (GRCm39) |
nonsense |
probably null |
|
R5503:Nsd1
|
UTSW |
13 |
55,393,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R5511:Nsd1
|
UTSW |
13 |
55,460,543 (GRCm39) |
missense |
probably benign |
0.00 |
R5683:Nsd1
|
UTSW |
13 |
55,393,961 (GRCm39) |
missense |
probably benign |
0.00 |
R5778:Nsd1
|
UTSW |
13 |
55,454,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R5793:Nsd1
|
UTSW |
13 |
55,395,819 (GRCm39) |
missense |
probably benign |
|
R5922:Nsd1
|
UTSW |
13 |
55,395,288 (GRCm39) |
missense |
probably benign |
0.01 |
R5956:Nsd1
|
UTSW |
13 |
55,411,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R6053:Nsd1
|
UTSW |
13 |
55,441,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R6141:Nsd1
|
UTSW |
13 |
55,439,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Nsd1
|
UTSW |
13 |
55,393,434 (GRCm39) |
missense |
probably benign |
|
R6224:Nsd1
|
UTSW |
13 |
55,460,945 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6396:Nsd1
|
UTSW |
13 |
55,386,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R6598:Nsd1
|
UTSW |
13 |
55,441,515 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7170:Nsd1
|
UTSW |
13 |
55,409,439 (GRCm39) |
nonsense |
probably null |
|
R7205:Nsd1
|
UTSW |
13 |
55,394,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R7215:Nsd1
|
UTSW |
13 |
55,395,454 (GRCm39) |
missense |
probably benign |
0.00 |
R7337:Nsd1
|
UTSW |
13 |
55,394,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R7432:Nsd1
|
UTSW |
13 |
55,361,187 (GRCm39) |
missense |
probably benign |
|
R7638:Nsd1
|
UTSW |
13 |
55,460,141 (GRCm39) |
missense |
probably benign |
0.01 |
R7647:Nsd1
|
UTSW |
13 |
55,447,648 (GRCm39) |
missense |
probably damaging |
0.96 |
R7658:Nsd1
|
UTSW |
13 |
55,425,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R7884:Nsd1
|
UTSW |
13 |
55,461,068 (GRCm39) |
missense |
probably damaging |
0.99 |
R8032:Nsd1
|
UTSW |
13 |
55,458,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R8113:Nsd1
|
UTSW |
13 |
55,393,434 (GRCm39) |
missense |
probably benign |
|
R8152:Nsd1
|
UTSW |
13 |
55,458,180 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8183:Nsd1
|
UTSW |
13 |
55,460,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R8432:Nsd1
|
UTSW |
13 |
55,395,516 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8462:Nsd1
|
UTSW |
13 |
55,446,189 (GRCm39) |
splice site |
probably null |
|
R8469:Nsd1
|
UTSW |
13 |
55,425,366 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8756:Nsd1
|
UTSW |
13 |
55,461,506 (GRCm39) |
missense |
probably benign |
0.00 |
R8867:Nsd1
|
UTSW |
13 |
55,430,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Nsd1
|
UTSW |
13 |
55,393,667 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9101:Nsd1
|
UTSW |
13 |
55,461,359 (GRCm39) |
missense |
|
|
R9154:Nsd1
|
UTSW |
13 |
55,361,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R9155:Nsd1
|
UTSW |
13 |
55,361,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R9262:Nsd1
|
UTSW |
13 |
55,394,871 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9592:Nsd1
|
UTSW |
13 |
55,424,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R9604:Nsd1
|
UTSW |
13 |
55,381,807 (GRCm39) |
missense |
probably benign |
0.25 |
R9712:Nsd1
|
UTSW |
13 |
55,393,856 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9716:Nsd1
|
UTSW |
13 |
55,458,313 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9787:Nsd1
|
UTSW |
13 |
55,461,518 (GRCm39) |
missense |
probably benign |
0.15 |
Z1088:Nsd1
|
UTSW |
13 |
55,361,661 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1176:Nsd1
|
UTSW |
13 |
55,393,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|