Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akt2 |
T |
A |
7: 27,328,824 (GRCm39) |
I182N |
probably damaging |
Het |
Alpk3 |
A |
G |
7: 80,728,255 (GRCm39) |
T462A |
probably benign |
Het |
Amz1 |
A |
G |
5: 140,738,014 (GRCm39) |
R425G |
probably damaging |
Het |
Aoc2 |
A |
G |
11: 101,217,201 (GRCm39) |
E428G |
probably damaging |
Het |
Car4 |
C |
T |
11: 84,856,593 (GRCm39) |
P294S |
probably damaging |
Het |
Chchd6 |
A |
T |
6: 89,396,762 (GRCm39) |
H216Q |
probably damaging |
Het |
Chl1 |
A |
G |
6: 103,675,086 (GRCm39) |
Y591C |
probably damaging |
Het |
Cln8 |
T |
C |
8: 14,945,178 (GRCm39) |
L164S |
probably damaging |
Het |
Dscaml1 |
T |
C |
9: 45,581,474 (GRCm39) |
I431T |
possibly damaging |
Het |
Fam234b |
T |
C |
6: 135,208,659 (GRCm39) |
L524P |
probably damaging |
Het |
Fmo1 |
T |
C |
1: 162,660,559 (GRCm39) |
N410S |
probably benign |
Het |
Ftsj3 |
G |
A |
11: 106,143,972 (GRCm39) |
R251* |
probably null |
Het |
Greb1l |
A |
T |
18: 10,515,200 (GRCm39) |
D555V |
probably damaging |
Het |
Hcar1 |
G |
T |
5: 124,017,135 (GRCm39) |
H185Q |
probably damaging |
Het |
Kcnj12 |
G |
A |
11: 60,960,319 (GRCm39) |
V206I |
probably benign |
Het |
Lamc3 |
G |
A |
2: 31,808,469 (GRCm39) |
G742S |
probably damaging |
Het |
Lipg |
T |
C |
18: 75,093,946 (GRCm39) |
|
probably null |
Het |
Ltbp2 |
A |
G |
12: 84,839,729 (GRCm39) |
|
probably null |
Het |
Mcm3ap |
T |
G |
10: 76,332,386 (GRCm39) |
Y1234* |
probably null |
Het |
Myh6 |
T |
A |
14: 55,194,612 (GRCm39) |
D719V |
possibly damaging |
Het |
Myo9b |
A |
G |
8: 71,743,689 (GRCm39) |
N250S |
probably damaging |
Het |
Nherf1 |
A |
G |
11: 115,070,858 (GRCm39) |
E270G |
probably benign |
Het |
Nphp1 |
G |
A |
2: 127,621,987 (GRCm39) |
Q47* |
probably null |
Het |
Nptx2 |
T |
C |
5: 144,493,056 (GRCm39) |
L381P |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 90,171,402 (GRCm39) |
N911S |
possibly damaging |
Het |
Or10j2 |
A |
T |
1: 173,097,972 (GRCm39) |
I77F |
probably benign |
Het |
Or5d46 |
T |
C |
2: 88,169,906 (GRCm39) |
|
probably benign |
Het |
P4ha1 |
T |
A |
10: 59,188,023 (GRCm39) |
F260Y |
probably benign |
Het |
Pitpnm2 |
T |
C |
5: 124,268,676 (GRCm39) |
D504G |
probably damaging |
Het |
Prss54 |
A |
G |
8: 96,292,237 (GRCm39) |
V114A |
probably benign |
Het |
Ptprc |
G |
A |
1: 137,998,957 (GRCm39) |
T1031M |
probably damaging |
Het |
Rtf2 |
T |
C |
2: 172,310,511 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,777,349 (GRCm39) |
|
probably benign |
Het |
Slc14a2 |
C |
T |
18: 78,206,341 (GRCm39) |
E492K |
probably damaging |
Het |
Stab1 |
G |
T |
14: 30,862,367 (GRCm39) |
N2322K |
probably damaging |
Het |
Thsd7b |
A |
G |
1: 130,087,369 (GRCm39) |
N1162S |
probably benign |
Het |
Tmprss11b |
T |
C |
5: 86,810,090 (GRCm39) |
I297V |
probably benign |
Het |
Tnn |
T |
C |
1: 159,972,775 (GRCm39) |
N276D |
probably benign |
Het |
Trhde |
A |
T |
10: 114,428,118 (GRCm39) |
|
probably benign |
Het |
Vmn1r115 |
T |
A |
7: 20,578,453 (GRCm39) |
H153L |
possibly damaging |
Het |
Vmn1r203 |
T |
A |
13: 22,708,997 (GRCm39) |
C259* |
probably null |
Het |
Xpot |
T |
A |
10: 121,451,109 (GRCm39) |
E97V |
probably damaging |
Het |
Zbtb2 |
T |
C |
10: 4,318,712 (GRCm39) |
D438G |
probably damaging |
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 |
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 |
R6629:Notch2
|
UTSW |
3 |
98,028,197 (GRCm39) |
missense |
possibly damaging |
0.65 |
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 |
|