Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300003K06Rik |
A |
C |
11: 99,728,840 (GRCm39) |
M1R |
probably null |
Het |
4930505A04Rik |
A |
C |
11: 30,404,815 (GRCm39) |
N29K |
probably benign |
Het |
Adamtsl4 |
T |
C |
3: 95,589,039 (GRCm39) |
Y464C |
probably damaging |
Het |
Asgr2 |
T |
C |
11: 69,989,072 (GRCm39) |
V172A |
probably damaging |
Het |
Atad1 |
T |
C |
19: 32,676,028 (GRCm39) |
Y132C |
probably damaging |
Het |
Bpifa6 |
G |
A |
2: 153,829,073 (GRCm39) |
R200H |
probably damaging |
Het |
Brd1 |
A |
T |
15: 88,572,558 (GRCm39) |
M1171K |
possibly damaging |
Het |
Cadm2 |
A |
T |
16: 66,461,281 (GRCm39) |
L392Q |
probably damaging |
Het |
Ccdc183 |
C |
T |
2: 25,500,594 (GRCm39) |
E333K |
possibly damaging |
Het |
Cenpe |
T |
C |
3: 134,949,536 (GRCm39) |
I1335T |
possibly damaging |
Het |
Cpxm2 |
T |
C |
7: 131,745,460 (GRCm39) |
N122D |
probably benign |
Het |
Crls1 |
T |
A |
2: 132,691,770 (GRCm39) |
|
probably null |
Het |
Cyp46a1 |
T |
C |
12: 108,327,819 (GRCm39) |
F460S |
probably damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dcps |
T |
A |
9: 35,047,777 (GRCm39) |
T128S |
probably benign |
Het |
Dcun1d3 |
A |
T |
7: 119,458,714 (GRCm39) |
L107* |
probably null |
Het |
Eml1 |
T |
C |
12: 108,480,767 (GRCm39) |
F397S |
probably damaging |
Het |
Fanca |
T |
A |
8: 124,032,020 (GRCm39) |
H348L |
possibly damaging |
Het |
Foxo1 |
T |
A |
3: 52,253,093 (GRCm39) |
S419T |
probably benign |
Het |
Gli3 |
T |
C |
13: 15,899,730 (GRCm39) |
V1039A |
probably benign |
Het |
Gng14 |
A |
T |
8: 85,794,220 (GRCm39) |
*73R |
probably null |
Het |
Gp6 |
A |
T |
7: 4,397,211 (GRCm39) |
F75I |
probably benign |
Het |
Gpha2 |
T |
A |
19: 6,277,142 (GRCm39) |
I81N |
possibly damaging |
Het |
Gspt1 |
C |
A |
16: 11,042,406 (GRCm39) |
V493L |
probably benign |
Het |
Igsf10 |
C |
A |
3: 59,232,931 (GRCm39) |
C1934F |
probably damaging |
Het |
Irgm1 |
T |
C |
11: 48,757,713 (GRCm39) |
T49A |
probably benign |
Het |
Klc4 |
A |
G |
17: 46,950,988 (GRCm39) |
I207T |
possibly damaging |
Het |
Krt1 |
A |
T |
15: 101,758,702 (GRCm39) |
V154D |
possibly damaging |
Het |
Lama1 |
T |
C |
17: 68,109,982 (GRCm39) |
V2201A |
possibly damaging |
Het |
Lilrb4a |
T |
A |
10: 51,367,745 (GRCm39) |
Y96N |
probably damaging |
Het |
Lrfn2 |
A |
G |
17: 49,403,379 (GRCm39) |
T501A |
probably damaging |
Het |
Lrriq1 |
A |
G |
10: 103,051,618 (GRCm39) |
I378T |
probably damaging |
Het |
Mphosph8 |
T |
C |
14: 56,905,810 (GRCm39) |
M1T |
probably null |
Het |
Ogdhl |
G |
A |
14: 32,064,018 (GRCm39) |
G647D |
probably benign |
Het |
Or5p57 |
T |
C |
7: 107,665,949 (GRCm39) |
I19V |
probably benign |
Het |
Or6c76b |
A |
G |
10: 129,693,061 (GRCm39) |
K225E |
probably benign |
Het |
Pbrm1 |
T |
A |
14: 30,772,068 (GRCm39) |
H387Q |
probably benign |
Het |
Pdgfrb |
C |
A |
18: 61,215,011 (GRCm39) |
Y1013* |
probably null |
Het |
Pitrm1 |
T |
C |
13: 6,615,090 (GRCm39) |
V562A |
probably damaging |
Het |
Pnpla8 |
T |
C |
12: 44,329,811 (GRCm39) |
V121A |
possibly damaging |
Het |
Psd4 |
T |
C |
2: 24,291,569 (GRCm39) |
L639P |
probably damaging |
Het |
Psmc3 |
G |
T |
2: 90,884,975 (GRCm39) |
R47L |
probably damaging |
Het |
Rptn |
C |
G |
3: 93,305,437 (GRCm39) |
H923Q |
possibly damaging |
Het |
Sesn2 |
A |
G |
4: 132,229,881 (GRCm39) |
V50A |
probably benign |
Het |
Skic3 |
C |
T |
13: 76,266,410 (GRCm39) |
T219M |
probably benign |
Het |
Slc6a16 |
G |
A |
7: 44,910,572 (GRCm39) |
G377S |
probably damaging |
Het |
Slitrk1 |
A |
G |
14: 109,149,454 (GRCm39) |
F419S |
probably damaging |
Het |
Slitrk5 |
GACTAC |
GACTACTAC |
14: 111,917,248 (GRCm39) |
|
probably benign |
Het |
Spata31d1a |
T |
A |
13: 59,854,134 (GRCm39) |
|
probably benign |
Homo |
Tgoln1 |
A |
T |
6: 72,592,984 (GRCm39) |
D165E |
possibly damaging |
Het |
Tmprss15 |
T |
A |
16: 78,821,266 (GRCm39) |
T492S |
probably benign |
Het |
Zc3h13 |
T |
A |
14: 75,574,849 (GRCm39) |
M1565K |
probably damaging |
Het |
Zcwpw1 |
T |
C |
5: 137,810,298 (GRCm39) |
V358A |
possibly damaging |
Het |
Zfp607a |
A |
G |
7: 27,578,007 (GRCm39) |
H359R |
probably damaging |
Het |
Zzef1 |
T |
A |
11: 72,746,209 (GRCm39) |
V837E |
probably damaging |
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 |
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 |
|
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 |
|