Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930563I02Rik |
A |
G |
14: 60,333,519 (GRCm39) |
|
probably benign |
Het |
Acaca |
T |
C |
11: 84,154,906 (GRCm39) |
M987T |
probably benign |
Het |
Acaca |
A |
G |
11: 84,185,809 (GRCm39) |
T115A |
possibly damaging |
Het |
Aknad1 |
A |
T |
3: 108,688,472 (GRCm39) |
D600V |
probably damaging |
Het |
Arfgef3 |
T |
A |
10: 18,492,701 (GRCm39) |
T1237S |
probably benign |
Het |
Brd4 |
A |
T |
17: 32,431,884 (GRCm39) |
L660Q |
probably benign |
Het |
Casp1 |
A |
G |
9: 5,306,213 (GRCm39) |
D366G |
possibly damaging |
Het |
Casp8ap2 |
C |
A |
4: 32,643,781 (GRCm39) |
S951R |
probably benign |
Het |
Chd9 |
A |
G |
8: 91,777,756 (GRCm39) |
E2589G |
probably damaging |
Het |
Dchs1 |
T |
C |
7: 105,413,411 (GRCm39) |
T1135A |
possibly damaging |
Het |
Dnhd1 |
T |
C |
7: 105,323,628 (GRCm39) |
V633A |
probably damaging |
Het |
Dock6 |
G |
T |
9: 21,750,973 (GRCm39) |
H400Q |
probably damaging |
Het |
Dzip1 |
A |
G |
14: 119,138,952 (GRCm39) |
F426L |
probably benign |
Het |
Elovl4 |
A |
G |
9: 83,662,826 (GRCm39) |
S236P |
probably damaging |
Het |
Emp1 |
T |
C |
6: 135,357,123 (GRCm39) |
F67S |
probably damaging |
Het |
Garnl3 |
A |
G |
2: 32,895,164 (GRCm39) |
L635P |
probably damaging |
Het |
Htr7 |
C |
A |
19: 35,946,703 (GRCm39) |
|
probably null |
Het |
Kcnd3 |
A |
C |
3: 105,576,442 (GRCm39) |
S629R |
probably benign |
Het |
Lrp2 |
T |
A |
2: 69,322,191 (GRCm39) |
I1913F |
possibly damaging |
Het |
Med19 |
T |
A |
2: 84,516,587 (GRCm39) |
D208E |
probably benign |
Het |
Mettl21c |
A |
T |
1: 44,052,792 (GRCm39) |
V75E |
probably damaging |
Het |
Nhsl3 |
T |
C |
4: 129,117,540 (GRCm39) |
T375A |
probably damaging |
Het |
Or10g3b |
A |
G |
14: 52,587,395 (GRCm39) |
I36T |
probably benign |
Het |
Or51v8 |
A |
T |
7: 103,319,674 (GRCm39) |
I188N |
probably damaging |
Het |
Or5p50 |
T |
A |
7: 107,422,007 (GRCm39) |
Y223F |
probably benign |
Het |
Peds1 |
T |
A |
2: 167,496,635 (GRCm39) |
Q46L |
possibly damaging |
Het |
Plat |
T |
A |
8: 23,266,881 (GRCm39) |
M291K |
probably benign |
Het |
Psmb4 |
T |
C |
3: 94,792,322 (GRCm39) |
E200G |
probably benign |
Het |
Reln |
T |
C |
5: 22,359,954 (GRCm39) |
Y190C |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,415,863 (GRCm39) |
S1750P |
probably damaging |
Het |
Slc5a4a |
T |
A |
10: 76,013,915 (GRCm39) |
|
probably null |
Het |
Sobp |
A |
T |
10: 43,034,034 (GRCm39) |
N97K |
possibly damaging |
Het |
Stac3 |
T |
C |
10: 127,339,229 (GRCm39) |
|
probably null |
Het |
Stat5b |
G |
T |
11: 100,687,318 (GRCm39) |
T436K |
probably damaging |
Het |
Tas1r3 |
A |
T |
4: 155,947,772 (GRCm39) |
M7K |
probably benign |
Het |
Vps13b |
C |
T |
15: 35,675,045 (GRCm39) |
Q1722* |
probably null |
Het |
Zfp677 |
A |
T |
17: 21,617,582 (GRCm39) |
Y213F |
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 |
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 |
R4080:Nsd1
|
UTSW |
13 |
55,449,622 (GRCm39) |
missense |
probably damaging |
0.96 |
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 |
|