Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aida |
T |
C |
1: 183,095,012 (GRCm39) |
V151A |
possibly damaging |
Het |
Akap3 |
T |
C |
6: 126,842,377 (GRCm39) |
V332A |
probably damaging |
Het |
Apobec3 |
T |
A |
15: 79,790,653 (GRCm39) |
W332R |
|
Het |
Atf6 |
A |
G |
1: 170,668,402 (GRCm39) |
V166A |
probably benign |
Het |
Bcl6b |
A |
G |
11: 70,118,858 (GRCm39) |
|
probably null |
Het |
Brd3 |
G |
T |
2: 27,340,373 (GRCm39) |
P612Q |
probably damaging |
Het |
Btg1 |
T |
A |
10: 96,453,263 (GRCm39) |
L26H |
probably damaging |
Het |
Btg4 |
A |
G |
9: 51,030,560 (GRCm39) |
D220G |
probably damaging |
Het |
Cd209e |
T |
C |
8: 3,901,183 (GRCm39) |
D157G |
probably benign |
Het |
Cdhr18 |
A |
T |
14: 13,814,959 (GRCm38) |
L858Q |
unknown |
Het |
Cimip2b |
T |
G |
4: 43,427,329 (GRCm39) |
T332P |
unknown |
Het |
Dnah10 |
T |
C |
5: 124,907,107 (GRCm39) |
L4269P |
probably damaging |
Het |
Dync1li2 |
C |
A |
8: 105,154,752 (GRCm39) |
K285N |
possibly damaging |
Het |
Ehmt2 |
C |
A |
17: 35,118,740 (GRCm39) |
Q198K |
possibly damaging |
Het |
Foxn3 |
C |
A |
12: 99,359,294 (GRCm39) |
|
probably benign |
Het |
Fstl4 |
C |
T |
11: 52,664,694 (GRCm39) |
P8L |
probably benign |
Het |
G6pc1 |
T |
C |
11: 101,258,660 (GRCm39) |
I13T |
possibly damaging |
Het |
Ghrhr |
A |
G |
6: 55,362,470 (GRCm39) |
I356V |
probably benign |
Het |
Gm14410 |
A |
T |
2: 176,885,773 (GRCm39) |
C164S |
probably damaging |
Het |
Gpcpd1 |
A |
T |
2: 132,388,848 (GRCm39) |
M308K |
possibly damaging |
Het |
Gpr143 |
GTTTTTT |
GTTTTTTT |
X: 151,578,627 (GRCm39) |
|
probably null |
Het |
Gpr179 |
T |
C |
11: 97,225,727 (GRCm39) |
K2143E |
probably benign |
Het |
Grm2 |
G |
A |
9: 106,524,408 (GRCm39) |
T298I |
probably damaging |
Het |
H2-T24 |
A |
T |
17: 36,326,455 (GRCm39) |
L148Q |
probably damaging |
Het |
Hcn2 |
C |
T |
10: 79,560,559 (GRCm39) |
R297C |
probably damaging |
Het |
Hic1 |
T |
C |
11: 75,056,757 (GRCm39) |
T711A |
possibly damaging |
Het |
Ide |
T |
C |
19: 37,264,514 (GRCm39) |
D672G |
|
Het |
Impg1 |
A |
G |
9: 80,288,923 (GRCm39) |
F378S |
probably damaging |
Het |
Lipe |
T |
C |
7: 25,098,128 (GRCm39) |
|
probably benign |
Het |
Lmo7 |
A |
G |
14: 102,156,136 (GRCm39) |
D1270G |
probably null |
Het |
Mbnl1 |
A |
T |
3: 60,520,859 (GRCm39) |
H149L |
probably damaging |
Het |
Mmel1 |
T |
C |
4: 154,978,592 (GRCm39) |
Y675H |
probably benign |
Het |
Mrfap1 |
C |
A |
5: 36,953,807 (GRCm39) |
R44L |
probably damaging |
Het |
Nherf2 |
G |
T |
17: 24,868,922 (GRCm39) |
T68K |
probably damaging |
Het |
Olfm3 |
A |
G |
3: 114,883,785 (GRCm39) |
D62G |
probably damaging |
Het |
Or10ak13 |
T |
C |
4: 118,638,952 (GRCm39) |
I277V |
probably benign |
Het |
Or2i1 |
C |
G |
17: 37,508,308 (GRCm39) |
A109P |
possibly damaging |
Het |
Or5g27 |
C |
T |
2: 85,409,882 (GRCm39) |
Q100* |
probably null |
Het |
Or5l13 |
T |
C |
2: 87,780,544 (GRCm39) |
E11G |
probably damaging |
Het |
Or5p59 |
T |
G |
7: 107,702,663 (GRCm39) |
I49S |
probably damaging |
Het |
Or6c8b |
T |
A |
10: 128,882,354 (GRCm39) |
I193F |
probably benign |
Het |
Pcbd2 |
A |
G |
13: 55,880,849 (GRCm39) |
Y68C |
probably benign |
Het |
Phf3 |
G |
C |
1: 30,869,003 (GRCm39) |
Q682E |
probably benign |
Het |
Ptpn6 |
C |
A |
6: 124,704,728 (GRCm39) |
R294L |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,025,026 (GRCm39) |
V1754D |
probably damaging |
Het |
Rab36 |
T |
A |
10: 74,887,873 (GRCm39) |
I248K |
probably damaging |
Het |
Rabac1 |
A |
G |
7: 24,671,579 (GRCm39) |
Y114H |
probably benign |
Het |
Rag1 |
A |
G |
2: 101,474,701 (GRCm39) |
V147A |
probably benign |
Het |
Rnf150 |
T |
A |
8: 83,717,144 (GRCm39) |
V217D |
probably damaging |
Het |
Scarf2 |
G |
T |
16: 17,620,473 (GRCm39) |
C101F |
probably damaging |
Het |
Sh3glb2 |
C |
T |
2: 30,236,672 (GRCm39) |
R230Q |
probably damaging |
Het |
Slc13a1 |
A |
G |
6: 24,089,100 (GRCm39) |
V550A |
probably damaging |
Het |
Sp140 |
A |
G |
1: 85,560,235 (GRCm39) |
N289S |
possibly damaging |
Het |
Spmip6 |
T |
C |
4: 41,505,091 (GRCm39) |
E207G |
|
Het |
Stac3 |
T |
A |
10: 127,338,654 (GRCm39) |
M1K |
probably null |
Het |
Stk31 |
C |
T |
6: 49,424,221 (GRCm39) |
T845I |
possibly damaging |
Het |
Sufu |
T |
C |
19: 46,385,674 (GRCm39) |
Y45H |
probably damaging |
Het |
Tg |
T |
A |
15: 66,607,109 (GRCm39) |
C1834* |
probably null |
Het |
Tns3 |
G |
A |
11: 8,401,142 (GRCm39) |
T1052M |
possibly damaging |
Het |
Tpcn1 |
T |
C |
5: 120,686,021 (GRCm39) |
T427A |
possibly damaging |
Het |
Trim45 |
A |
G |
3: 100,830,265 (GRCm39) |
H13R |
probably benign |
Het |
Trpv5 |
A |
G |
6: 41,647,773 (GRCm39) |
F347L |
probably benign |
Het |
Vmn1r43 |
G |
A |
6: 89,846,877 (GRCm39) |
T203M |
probably damaging |
Het |
Zfp236 |
G |
T |
18: 82,664,238 (GRCm39) |
Q516K |
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 |
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 |
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 |
|