Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atxn3 |
A |
T |
12: 101,903,665 (GRCm39) |
M180K |
probably benign |
Het |
Bnip2 |
G |
T |
9: 69,909,393 (GRCm39) |
R236L |
probably null |
Het |
Boc |
T |
C |
16: 44,312,724 (GRCm39) |
D582G |
probably benign |
Het |
Cacul1 |
T |
C |
19: 60,568,805 (GRCm39) |
S118G |
probably benign |
Het |
Ccdc192 |
T |
C |
18: 57,863,852 (GRCm39) |
S219P |
possibly damaging |
Het |
Cpa2 |
A |
T |
6: 30,554,193 (GRCm39) |
D271V |
probably damaging |
Het |
Cubn |
G |
A |
2: 13,435,683 (GRCm39) |
T1091M |
probably damaging |
Het |
Dlgap2 |
A |
G |
8: 14,881,465 (GRCm39) |
T846A |
probably benign |
Het |
Eif5 |
G |
T |
12: 111,510,042 (GRCm39) |
A329S |
probably damaging |
Het |
Fam136b-ps |
G |
A |
15: 31,276,962 (GRCm39) |
|
probably benign |
Het |
Gnrhr |
A |
G |
5: 86,330,168 (GRCm39) |
V284A |
probably benign |
Het |
Grin3a |
A |
G |
4: 49,844,991 (GRCm39) |
S31P |
probably damaging |
Het |
Hectd2 |
T |
C |
19: 36,592,938 (GRCm39) |
L701P |
probably damaging |
Het |
Hook1 |
C |
T |
4: 95,889,507 (GRCm39) |
T241I |
probably benign |
Het |
Kif5a |
A |
G |
10: 127,084,123 (GRCm39) |
V52A |
probably damaging |
Het |
Lasp1 |
T |
A |
11: 97,697,722 (GRCm39) |
Y11* |
probably null |
Het |
Meltf |
A |
G |
16: 31,703,894 (GRCm39) |
Y207C |
probably damaging |
Het |
Mllt3 |
ACTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTACTACTACTGCTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTGCTGCTGCT |
ACTGCTGCTGCTGCTGCTACTGCTGCTGCTGCTGCTGCTACTACTACTGCTGCTGCTGCTGCTGCTGCTACTGCTGCTGCTGCTGCTGCT |
4: 87,759,504 (GRCm39) |
|
probably benign |
Het |
Nek1 |
A |
G |
8: 61,507,367 (GRCm39) |
|
probably null |
Het |
Or4c116 |
T |
A |
2: 88,942,506 (GRCm39) |
M117L |
probably benign |
Het |
Pcnx2 |
C |
T |
8: 126,617,851 (GRCm39) |
G135R |
probably benign |
Het |
Pla2g4f |
A |
T |
2: 120,138,723 (GRCm39) |
L242Q |
probably damaging |
Het |
Plcxd2 |
T |
G |
16: 45,785,470 (GRCm39) |
T312P |
probably damaging |
Het |
Prpf4 |
G |
A |
4: 62,336,097 (GRCm39) |
V275I |
possibly damaging |
Het |
Prpf8 |
G |
A |
11: 75,386,252 (GRCm39) |
|
probably null |
Het |
Pxn |
T |
C |
5: 115,692,121 (GRCm39) |
L401P |
probably damaging |
Het |
Rab44 |
A |
T |
17: 29,354,754 (GRCm39) |
|
probably benign |
Het |
Rfx6 |
C |
A |
10: 51,601,586 (GRCm39) |
T669K |
probably benign |
Het |
Rgs16 |
A |
G |
1: 153,619,420 (GRCm39) |
N142S |
probably damaging |
Het |
Rhobtb1 |
A |
G |
10: 69,106,146 (GRCm39) |
E237G |
possibly damaging |
Het |
Rsbn1 |
A |
C |
3: 103,835,757 (GRCm39) |
D265A |
probably damaging |
Het |
Rufy4 |
A |
G |
1: 74,171,526 (GRCm39) |
|
probably null |
Het |
Slc4a1 |
C |
A |
11: 102,252,048 (GRCm39) |
E19* |
probably null |
Het |
Tctn1 |
A |
G |
5: 122,380,731 (GRCm39) |
S526P |
probably damaging |
Het |
Tspear |
A |
T |
10: 77,706,343 (GRCm39) |
H371L |
probably benign |
Het |
Vmn1r34 |
A |
T |
6: 66,614,499 (GRCm39) |
F80I |
probably benign |
Het |
Wdr75 |
G |
A |
1: 45,851,216 (GRCm39) |
S264N |
probably damaging |
Het |
Zfp652 |
A |
T |
11: 95,654,616 (GRCm39) |
N340Y |
probably damaging |
Het |
Zp3 |
A |
G |
5: 136,016,190 (GRCm39) |
T306A |
probably benign |
Het |
|
Other mutations in Notch2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00675:Notch2
|
APN |
3 |
98,018,991 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01517:Notch2
|
APN |
3 |
98,045,971 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01630:Notch2
|
APN |
3 |
98,053,934 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01637:Notch2
|
APN |
3 |
98,053,376 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01828:Notch2
|
APN |
3 |
97,979,929 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01998:Notch2
|
APN |
3 |
98,050,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02008:Notch2
|
APN |
3 |
98,054,612 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02030:Notch2
|
APN |
3 |
98,006,737 (GRCm39) |
splice site |
probably null |
|
IGL02155:Notch2
|
APN |
3 |
98,045,806 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02268:Notch2
|
APN |
3 |
98,044,713 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02301:Notch2
|
APN |
3 |
98,048,870 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02336:Notch2
|
APN |
3 |
98,045,711 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02340:Notch2
|
APN |
3 |
98,054,652 (GRCm39) |
nonsense |
probably null |
|
IGL02536:Notch2
|
APN |
3 |
98,009,723 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02589:Notch2
|
APN |
3 |
98,011,663 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02633:Notch2
|
APN |
3 |
98,024,013 (GRCm39) |
splice site |
probably benign |
|
IGL02691:Notch2
|
APN |
3 |
98,042,923 (GRCm39) |
nonsense |
probably null |
|
IGL02832:Notch2
|
APN |
3 |
98,044,689 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02894:Notch2
|
APN |
3 |
98,009,748 (GRCm39) |
nonsense |
probably null |
|
IGL02902:Notch2
|
APN |
3 |
98,018,890 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02967:Notch2
|
APN |
3 |
98,053,460 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03015:Notch2
|
APN |
3 |
97,979,965 (GRCm39) |
missense |
possibly damaging |
0.83 |
PIT4378001:Notch2
|
UTSW |
3 |
98,050,272 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4519001:Notch2
|
UTSW |
3 |
98,005,424 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4581001:Notch2
|
UTSW |
3 |
98,011,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R0111:Notch2
|
UTSW |
3 |
98,046,077 (GRCm39) |
missense |
probably benign |
0.00 |
R0129:Notch2
|
UTSW |
3 |
98,053,936 (GRCm39) |
missense |
probably benign |
0.08 |
R0143:Notch2
|
UTSW |
3 |
98,053,433 (GRCm39) |
missense |
probably damaging |
0.99 |
R0480:Notch2
|
UTSW |
3 |
98,053,853 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0523:Notch2
|
UTSW |
3 |
98,018,914 (GRCm39) |
missense |
probably benign |
0.00 |
R0523:Notch2
|
UTSW |
3 |
97,978,286 (GRCm39) |
missense |
probably benign |
0.34 |
R0531:Notch2
|
UTSW |
3 |
98,009,767 (GRCm39) |
splice site |
probably benign |
|
R0537:Notch2
|
UTSW |
3 |
98,024,057 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0987:Notch2
|
UTSW |
3 |
98,041,993 (GRCm39) |
splice site |
probably null |
|
R1485:Notch2
|
UTSW |
3 |
98,007,573 (GRCm39) |
missense |
probably benign |
0.00 |
R1555:Notch2
|
UTSW |
3 |
98,038,656 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1625:Notch2
|
UTSW |
3 |
98,018,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R1699:Notch2
|
UTSW |
3 |
98,052,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R1765:Notch2
|
UTSW |
3 |
98,029,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R1794:Notch2
|
UTSW |
3 |
98,006,863 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1974:Notch2
|
UTSW |
3 |
97,980,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R2086:Notch2
|
UTSW |
3 |
98,009,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R2099:Notch2
|
UTSW |
3 |
98,022,637 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3778:Notch2
|
UTSW |
3 |
98,053,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R3924:Notch2
|
UTSW |
3 |
98,029,350 (GRCm39) |
nonsense |
probably null |
|
R4018:Notch2
|
UTSW |
3 |
98,011,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R4151:Notch2
|
UTSW |
3 |
98,054,387 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4417:Notch2
|
UTSW |
3 |
98,038,586 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4510:Notch2
|
UTSW |
3 |
98,053,637 (GRCm39) |
missense |
probably benign |
0.02 |
R4511:Notch2
|
UTSW |
3 |
98,053,637 (GRCm39) |
missense |
probably benign |
0.02 |
R4636:Notch2
|
UTSW |
3 |
98,053,420 (GRCm39) |
missense |
probably benign |
0.02 |
R4661:Notch2
|
UTSW |
3 |
98,042,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R4856:Notch2
|
UTSW |
3 |
98,009,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R4886:Notch2
|
UTSW |
3 |
98,009,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R4945:Notch2
|
UTSW |
3 |
98,019,037 (GRCm39) |
missense |
probably benign |
0.01 |
R4970:Notch2
|
UTSW |
3 |
98,008,952 (GRCm39) |
critical splice donor site |
probably null |
|
R4974:Notch2
|
UTSW |
3 |
98,046,949 (GRCm39) |
missense |
probably benign |
0.39 |
R5082:Notch2
|
UTSW |
3 |
98,007,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Notch2
|
UTSW |
3 |
98,008,952 (GRCm39) |
critical splice donor site |
probably null |
|
R5156:Notch2
|
UTSW |
3 |
98,031,626 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5433:Notch2
|
UTSW |
3 |
98,033,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R5539:Notch2
|
UTSW |
3 |
98,044,898 (GRCm39) |
missense |
probably damaging |
0.99 |
R5813:Notch2
|
UTSW |
3 |
98,042,744 (GRCm39) |
missense |
probably benign |
|
R5827:Notch2
|
UTSW |
3 |
97,980,178 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5908:Notch2
|
UTSW |
3 |
98,031,239 (GRCm39) |
intron |
probably benign |
|
R6021:Notch2
|
UTSW |
3 |
98,029,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R6090:Notch2
|
UTSW |
3 |
98,042,693 (GRCm39) |
nonsense |
probably null |
|
R6103:Notch2
|
UTSW |
3 |
98,043,059 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6111:Notch2
|
UTSW |
3 |
98,053,609 (GRCm39) |
missense |
probably benign |
0.00 |
R6168:Notch2
|
UTSW |
3 |
98,052,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R6382:Notch2
|
UTSW |
3 |
98,048,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6404:Notch2
|
UTSW |
3 |
97,989,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R6419:Notch2
|
UTSW |
3 |
98,007,705 (GRCm39) |
critical splice donor site |
probably null |
|
R6454:Notch2
|
UTSW |
3 |
98,044,722 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6626:Notch2
|
UTSW |
3 |
98,008,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R6706:Notch2
|
UTSW |
3 |
98,045,746 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6735:Notch2
|
UTSW |
3 |
98,041,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R6837:Notch2
|
UTSW |
3 |
97,978,170 (GRCm39) |
splice site |
probably null |
|
R7021:Notch2
|
UTSW |
3 |
98,042,762 (GRCm39) |
missense |
probably benign |
|
R7028:Notch2
|
UTSW |
3 |
98,009,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R7228:Notch2
|
UTSW |
3 |
98,044,633 (GRCm39) |
nonsense |
probably null |
|
R7320:Notch2
|
UTSW |
3 |
98,038,643 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7361:Notch2
|
UTSW |
3 |
98,038,718 (GRCm39) |
missense |
probably benign |
0.04 |
R7562:Notch2
|
UTSW |
3 |
98,020,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R7630:Notch2
|
UTSW |
3 |
98,044,824 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7637:Notch2
|
UTSW |
3 |
98,053,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7748:Notch2
|
UTSW |
3 |
98,045,800 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7764:Notch2
|
UTSW |
3 |
98,050,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R7817:Notch2
|
UTSW |
3 |
98,014,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R7952:Notch2
|
UTSW |
3 |
98,007,552 (GRCm39) |
missense |
probably benign |
0.30 |
R8136:Notch2
|
UTSW |
3 |
98,031,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R8159:Notch2
|
UTSW |
3 |
98,028,238 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8679:Notch2
|
UTSW |
3 |
98,029,218 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8879:Notch2
|
UTSW |
3 |
98,042,915 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9146:Notch2
|
UTSW |
3 |
98,011,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R9398:Notch2
|
UTSW |
3 |
98,009,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R9422:Notch2
|
UTSW |
3 |
98,054,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R9594:Notch2
|
UTSW |
3 |
98,041,889 (GRCm39) |
missense |
possibly damaging |
0.63 |
|