Other mutations in this stock |
Total: 114 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Acot6 |
A |
G |
12: 84,155,789 (GRCm39) |
K246E |
probably benign |
Het |
Actl11 |
T |
A |
9: 107,808,615 (GRCm39) |
H979Q |
probably damaging |
Het |
Adal |
T |
A |
2: 120,986,030 (GRCm39) |
|
probably benign |
Het |
Add2 |
G |
A |
6: 86,087,840 (GRCm39) |
V596I |
probably benign |
Het |
Adrb3 |
A |
C |
8: 27,717,798 (GRCm39) |
M217R |
probably damaging |
Het |
Ank1 |
T |
C |
8: 23,631,134 (GRCm39) |
|
probably benign |
Het |
Ank2 |
A |
T |
3: 126,757,094 (GRCm39) |
N1054K |
possibly damaging |
Het |
Ankib1 |
T |
C |
5: 3,763,217 (GRCm39) |
Y504C |
probably damaging |
Het |
Ankrd29 |
T |
C |
18: 12,395,242 (GRCm39) |
K217R |
probably damaging |
Het |
Ankrd45 |
T |
C |
1: 160,982,876 (GRCm39) |
V129A |
probably damaging |
Het |
Aox4 |
A |
T |
1: 58,275,835 (GRCm39) |
D389V |
probably benign |
Het |
Aph1a |
G |
T |
3: 95,802,843 (GRCm39) |
G148W |
probably damaging |
Het |
Arhgef26 |
G |
A |
3: 62,247,806 (GRCm39) |
D297N |
possibly damaging |
Het |
Atxn7l3b |
C |
A |
10: 112,764,649 (GRCm39) |
|
probably benign |
Het |
Auh |
A |
G |
13: 52,995,065 (GRCm39) |
S167P |
probably damaging |
Het |
Bach1 |
A |
T |
16: 87,515,888 (GRCm39) |
K143I |
possibly damaging |
Het |
Bbx |
T |
A |
16: 50,045,101 (GRCm39) |
T487S |
probably damaging |
Het |
Bche |
T |
G |
3: 73,609,177 (GRCm39) |
D83A |
probably benign |
Het |
Bri3bp |
G |
T |
5: 125,518,760 (GRCm39) |
|
probably benign |
Het |
Cd3d |
A |
T |
9: 44,896,296 (GRCm39) |
E28D |
probably damaging |
Het |
Cdc42bpa |
A |
G |
1: 179,965,366 (GRCm39) |
T1028A |
probably damaging |
Het |
Ceacam23 |
A |
G |
7: 17,639,143 (GRCm39) |
|
probably null |
Het |
Celsr2 |
T |
C |
3: 108,319,945 (GRCm39) |
I956V |
possibly damaging |
Het |
Cep95 |
A |
T |
11: 106,707,480 (GRCm39) |
|
probably null |
Het |
Cic |
G |
T |
7: 24,986,535 (GRCm39) |
G1289C |
probably damaging |
Het |
Cndp1 |
A |
G |
18: 84,650,025 (GRCm39) |
Y223H |
probably damaging |
Het |
Cops8 |
A |
G |
1: 90,538,724 (GRCm39) |
D51G |
probably damaging |
Het |
Csgalnact1 |
T |
C |
8: 68,913,623 (GRCm39) |
E194G |
probably benign |
Het |
Ctsm |
A |
G |
13: 61,686,776 (GRCm39) |
Y39H |
probably damaging |
Het |
Dhrs2 |
T |
C |
14: 55,474,722 (GRCm39) |
V119A |
probably damaging |
Het |
Drosha |
T |
A |
15: 12,935,093 (GRCm39) |
M1336K |
probably benign |
Het |
Dsp |
G |
A |
13: 38,381,678 (GRCm39) |
D2808N |
possibly damaging |
Het |
Ehmt1 |
G |
T |
2: 24,767,509 (GRCm39) |
P135T |
probably damaging |
Het |
Epas1 |
A |
G |
17: 87,116,882 (GRCm39) |
N184S |
probably damaging |
Het |
Erich3 |
C |
T |
3: 154,454,025 (GRCm39) |
T597I |
possibly damaging |
Het |
F10 |
T |
C |
8: 13,105,698 (GRCm39) |
V421A |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fam227b |
G |
A |
2: 125,958,043 (GRCm39) |
P241S |
probably damaging |
Het |
Fcgrt |
C |
T |
7: 44,751,372 (GRCm39) |
G192D |
probably benign |
Het |
Fras1 |
A |
G |
5: 96,798,541 (GRCm39) |
E1184G |
possibly damaging |
Het |
Garre1 |
A |
C |
7: 33,945,225 (GRCm39) |
Y552D |
probably damaging |
Het |
Grn |
C |
A |
11: 102,321,380 (GRCm39) |
|
probably benign |
Het |
Gvin-ps5 |
A |
T |
7: 105,928,664 (GRCm39) |
|
noncoding transcript |
Het |
Hadh |
A |
T |
3: 131,029,197 (GRCm39) |
L274* |
probably null |
Het |
Hus1 |
T |
C |
11: 8,956,027 (GRCm39) |
S169G |
probably damaging |
Het |
Hydin |
A |
T |
8: 111,290,554 (GRCm39) |
I3338F |
possibly damaging |
Het |
Ighv11-1 |
T |
G |
12: 113,945,768 (GRCm39) |
E28D |
probably benign |
Het |
Kctd9 |
C |
T |
14: 67,966,805 (GRCm39) |
T106I |
probably damaging |
Het |
Krit1 |
A |
T |
5: 3,872,238 (GRCm39) |
N421I |
probably damaging |
Het |
Lamb1 |
A |
G |
12: 31,376,677 (GRCm39) |
D1619G |
probably damaging |
Het |
Lpar6 |
G |
A |
14: 73,476,147 (GRCm39) |
C36Y |
probably damaging |
Het |
Lrrc37a |
G |
C |
11: 103,347,565 (GRCm39) |
F3043L |
unknown |
Het |
Lrrc46 |
A |
T |
11: 96,931,765 (GRCm39) |
V19D |
probably damaging |
Het |
Mapkap1 |
G |
T |
2: 34,471,303 (GRCm39) |
S197I |
probably damaging |
Het |
Mrps35 |
A |
C |
6: 146,961,645 (GRCm39) |
K173N |
possibly damaging |
Het |
Mtf2 |
A |
G |
5: 108,220,894 (GRCm39) |
|
probably benign |
Het |
Ncf1 |
A |
C |
5: 134,252,267 (GRCm39) |
D261E |
probably damaging |
Het |
Nrxn1 |
A |
T |
17: 90,928,274 (GRCm39) |
|
probably benign |
Het |
Or13a18 |
C |
A |
7: 140,190,304 (GRCm39) |
A75E |
possibly damaging |
Het |
Or4x13 |
T |
A |
2: 90,231,107 (GRCm39) |
M34K |
probably benign |
Het |
Or52a33 |
A |
G |
7: 103,289,308 (GRCm39) |
F13S |
probably damaging |
Het |
Or5k3 |
T |
C |
16: 58,969,981 (GRCm39) |
L256P |
probably damaging |
Het |
Or5v1 |
G |
T |
17: 37,810,017 (GRCm39) |
L158F |
probably benign |
Het |
Otud4 |
G |
A |
8: 80,382,318 (GRCm39) |
V176I |
probably damaging |
Het |
Pakap |
T |
A |
4: 57,856,552 (GRCm39) |
V668E |
probably benign |
Het |
Papolg |
T |
C |
11: 23,823,919 (GRCm39) |
|
probably null |
Het |
Pgk2 |
A |
G |
17: 40,518,402 (GRCm39) |
V342A |
probably damaging |
Het |
Phf2 |
G |
A |
13: 48,961,320 (GRCm39) |
A790V |
unknown |
Het |
Prkdc |
T |
C |
16: 15,491,861 (GRCm39) |
I602T |
possibly damaging |
Het |
Prl3d3 |
T |
C |
13: 27,343,072 (GRCm39) |
I86T |
possibly damaging |
Het |
Prss8 |
G |
T |
7: 127,525,635 (GRCm39) |
Q295K |
probably benign |
Het |
Ptpre |
C |
T |
7: 135,270,861 (GRCm39) |
H346Y |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Pwwp3a |
T |
C |
10: 80,068,702 (GRCm39) |
L282P |
probably benign |
Het |
Qrfpr |
A |
G |
3: 36,276,285 (GRCm39) |
V35A |
probably damaging |
Het |
Rpf1 |
A |
G |
3: 146,212,293 (GRCm39) |
L349S |
probably damaging |
Het |
Rpl41 |
G |
T |
10: 128,384,652 (GRCm39) |
|
probably null |
Het |
Rprd2 |
G |
C |
3: 95,672,632 (GRCm39) |
R924G |
probably benign |
Het |
Serpini1 |
T |
A |
3: 75,521,795 (GRCm39) |
N95K |
probably benign |
Het |
Sfxn1 |
A |
T |
13: 54,242,933 (GRCm39) |
T64S |
probably benign |
Het |
Siae |
T |
G |
9: 37,557,816 (GRCm39) |
I541S |
possibly damaging |
Het |
Slc25a4 |
T |
A |
8: 46,660,509 (GRCm39) |
K296N |
probably benign |
Het |
Slc37a1 |
A |
G |
17: 31,541,120 (GRCm39) |
N204S |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,413,800 (GRCm39) |
N976S |
probably benign |
Het |
Smarcal1 |
T |
C |
1: 72,672,019 (GRCm39) |
S847P |
possibly damaging |
Het |
Smg1 |
A |
T |
7: 117,757,323 (GRCm39) |
|
probably benign |
Het |
Smg1 |
C |
T |
7: 117,807,274 (GRCm39) |
A168T |
probably benign |
Het |
Sptlc1 |
A |
G |
13: 53,505,692 (GRCm39) |
I242T |
probably damaging |
Het |
St8sia2 |
T |
C |
7: 73,616,709 (GRCm39) |
I89V |
possibly damaging |
Het |
Supt20 |
A |
T |
3: 54,602,555 (GRCm39) |
|
probably benign |
Het |
Tep1 |
T |
C |
14: 51,076,457 (GRCm39) |
D1659G |
probably benign |
Het |
Tex10 |
C |
A |
4: 48,458,525 (GRCm39) |
|
probably benign |
Het |
Thbs3 |
CAGAAG |
CAG |
3: 89,130,409 (GRCm39) |
|
probably benign |
Het |
Tmbim6 |
C |
A |
15: 99,299,950 (GRCm39) |
S22* |
probably null |
Het |
Tmc2 |
A |
T |
2: 130,043,961 (GRCm39) |
K65M |
possibly damaging |
Het |
Tmod1 |
A |
G |
4: 46,090,872 (GRCm39) |
S142G |
probably damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trmt6 |
T |
C |
2: 132,650,191 (GRCm39) |
R349G |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,537,586 (GRCm39) |
T26454S |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,605,122 (GRCm39) |
V16555I |
probably benign |
Het |
Tut4 |
T |
A |
4: 108,384,042 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
T |
C |
2: 69,850,790 (GRCm39) |
|
probably benign |
Het |
Vmn1r17 |
A |
C |
6: 57,337,460 (GRCm39) |
F253V |
possibly damaging |
Het |
Vmn1r201 |
G |
T |
13: 22,659,622 (GRCm39) |
A279S |
possibly damaging |
Het |
Vmn2r17 |
A |
T |
5: 109,575,739 (GRCm39) |
R203S |
probably benign |
Het |
Vwa5a |
A |
G |
9: 38,633,926 (GRCm39) |
E43G |
probably benign |
Het |
Wdr86 |
C |
T |
5: 24,917,843 (GRCm39) |
|
probably null |
Het |
Wdsub1 |
A |
T |
2: 59,700,758 (GRCm39) |
|
probably benign |
Het |
Zcchc7 |
T |
C |
4: 44,931,039 (GRCm39) |
L76P |
probably damaging |
Het |
Zfp108 |
G |
T |
7: 23,960,163 (GRCm39) |
K251N |
probably benign |
Het |
Zfp263 |
T |
C |
16: 3,566,992 (GRCm39) |
C148R |
probably damaging |
Het |
Zfp687 |
A |
C |
3: 94,917,697 (GRCm39) |
F692V |
probably damaging |
Het |
|
Other mutations in Notch1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00164:Notch1
|
APN |
2 |
26,350,058 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01343:Notch1
|
APN |
2 |
26,362,917 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02066:Notch1
|
APN |
2 |
26,350,408 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02158:Notch1
|
APN |
2 |
26,350,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02541:Notch1
|
APN |
2 |
26,358,515 (GRCm39) |
missense |
probably benign |
0.12 |
IGL03280:Notch1
|
APN |
2 |
26,367,886 (GRCm39) |
intron |
probably benign |
|
IGL03338:Notch1
|
APN |
2 |
26,349,971 (GRCm39) |
missense |
probably benign |
|
Antero
|
UTSW |
2 |
26,366,126 (GRCm39) |
missense |
possibly damaging |
0.96 |
march
|
UTSW |
2 |
26,359,911 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4494001:Notch1
|
UTSW |
2 |
26,356,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Notch1
|
UTSW |
2 |
26,363,830 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0025:Notch1
|
UTSW |
2 |
26,360,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R0129:Notch1
|
UTSW |
2 |
26,350,470 (GRCm39) |
missense |
probably benign |
0.06 |
R0285:Notch1
|
UTSW |
2 |
26,350,873 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0531:Notch1
|
UTSW |
2 |
26,356,584 (GRCm39) |
missense |
probably benign |
0.00 |
R0747:Notch1
|
UTSW |
2 |
26,362,152 (GRCm39) |
missense |
unknown |
|
R1440:Notch1
|
UTSW |
2 |
26,370,976 (GRCm39) |
intron |
probably benign |
|
R1502:Notch1
|
UTSW |
2 |
26,374,335 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1539:Notch1
|
UTSW |
2 |
26,362,125 (GRCm39) |
nonsense |
probably null |
|
R1623:Notch1
|
UTSW |
2 |
26,368,624 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1844:Notch1
|
UTSW |
2 |
26,350,446 (GRCm39) |
missense |
probably benign |
0.12 |
R1863:Notch1
|
UTSW |
2 |
26,359,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Notch1
|
UTSW |
2 |
26,371,591 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1926:Notch1
|
UTSW |
2 |
26,371,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R2156:Notch1
|
UTSW |
2 |
26,350,873 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2196:Notch1
|
UTSW |
2 |
26,353,816 (GRCm39) |
nonsense |
probably null |
|
R2209:Notch1
|
UTSW |
2 |
26,350,019 (GRCm39) |
missense |
probably benign |
|
R2382:Notch1
|
UTSW |
2 |
26,363,793 (GRCm39) |
missense |
probably benign |
0.40 |
R2508:Notch1
|
UTSW |
2 |
26,355,485 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2873:Notch1
|
UTSW |
2 |
26,350,247 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2874:Notch1
|
UTSW |
2 |
26,350,247 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3798:Notch1
|
UTSW |
2 |
26,368,630 (GRCm39) |
missense |
probably benign |
0.00 |
R4019:Notch1
|
UTSW |
2 |
26,371,154 (GRCm39) |
missense |
probably benign |
0.03 |
R4305:Notch1
|
UTSW |
2 |
26,367,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R4334:Notch1
|
UTSW |
2 |
26,350,048 (GRCm39) |
missense |
probably benign |
0.22 |
R4504:Notch1
|
UTSW |
2 |
26,362,189 (GRCm39) |
missense |
probably benign |
0.16 |
R4624:Notch1
|
UTSW |
2 |
26,368,093 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4659:Notch1
|
UTSW |
2 |
26,360,901 (GRCm39) |
missense |
probably damaging |
0.99 |
R4703:Notch1
|
UTSW |
2 |
26,361,170 (GRCm39) |
missense |
probably benign |
|
R4869:Notch1
|
UTSW |
2 |
26,361,191 (GRCm39) |
missense |
probably benign |
0.21 |
R4938:Notch1
|
UTSW |
2 |
26,364,136 (GRCm39) |
nonsense |
probably null |
|
R5010:Notch1
|
UTSW |
2 |
26,366,126 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5283:Notch1
|
UTSW |
2 |
26,358,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R5303:Notch1
|
UTSW |
2 |
26,368,631 (GRCm39) |
missense |
probably benign |
0.01 |
R5635:Notch1
|
UTSW |
2 |
26,366,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R5755:Notch1
|
UTSW |
2 |
26,363,704 (GRCm39) |
missense |
probably benign |
0.12 |
R5926:Notch1
|
UTSW |
2 |
26,366,116 (GRCm39) |
missense |
probably benign |
0.35 |
R5947:Notch1
|
UTSW |
2 |
26,352,540 (GRCm39) |
intron |
probably benign |
|
R6053:Notch1
|
UTSW |
2 |
26,362,924 (GRCm39) |
missense |
probably benign |
0.06 |
R6161:Notch1
|
UTSW |
2 |
26,358,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R6162:Notch1
|
UTSW |
2 |
26,352,207 (GRCm39) |
missense |
probably benign |
|
R6174:Notch1
|
UTSW |
2 |
26,375,454 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6199:Notch1
|
UTSW |
2 |
26,359,911 (GRCm39) |
missense |
probably damaging |
0.98 |
R6209:Notch1
|
UTSW |
2 |
26,362,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Notch1
|
UTSW |
2 |
26,364,182 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6493:Notch1
|
UTSW |
2 |
26,362,110 (GRCm39) |
missense |
unknown |
|
R6723:Notch1
|
UTSW |
2 |
26,368,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R6736:Notch1
|
UTSW |
2 |
26,350,298 (GRCm39) |
missense |
probably benign |
0.01 |
R7020:Notch1
|
UTSW |
2 |
26,371,586 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7058:Notch1
|
UTSW |
2 |
26,353,830 (GRCm39) |
missense |
probably benign |
0.05 |
R7154:Notch1
|
UTSW |
2 |
26,349,950 (GRCm39) |
missense |
probably benign |
|
R7291:Notch1
|
UTSW |
2 |
26,366,387 (GRCm39) |
missense |
probably benign |
0.01 |
R7379:Notch1
|
UTSW |
2 |
26,369,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R7560:Notch1
|
UTSW |
2 |
26,350,177 (GRCm39) |
missense |
probably benign |
0.43 |
R7610:Notch1
|
UTSW |
2 |
26,368,191 (GRCm39) |
missense |
probably benign |
0.13 |
R7833:Notch1
|
UTSW |
2 |
26,349,545 (GRCm39) |
makesense |
probably null |
|
R7988:Notch1
|
UTSW |
2 |
26,361,013 (GRCm39) |
missense |
probably benign |
0.00 |
R8493:Notch1
|
UTSW |
2 |
26,362,251 (GRCm39) |
missense |
unknown |
|
R8514:Notch1
|
UTSW |
2 |
26,362,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R8523:Notch1
|
UTSW |
2 |
26,354,917 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8677:Notch1
|
UTSW |
2 |
26,359,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R8696:Notch1
|
UTSW |
2 |
26,368,004 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8833:Notch1
|
UTSW |
2 |
26,371,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R8964:Notch1
|
UTSW |
2 |
26,371,062 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9091:Notch1
|
UTSW |
2 |
26,369,895 (GRCm39) |
missense |
probably damaging |
0.99 |
R9144:Notch1
|
UTSW |
2 |
26,349,587 (GRCm39) |
missense |
probably benign |
0.00 |
R9145:Notch1
|
UTSW |
2 |
26,349,587 (GRCm39) |
missense |
probably benign |
0.00 |
R9151:Notch1
|
UTSW |
2 |
26,367,939 (GRCm39) |
missense |
probably benign |
0.01 |
R9270:Notch1
|
UTSW |
2 |
26,369,895 (GRCm39) |
missense |
probably damaging |
0.99 |
R9463:Notch1
|
UTSW |
2 |
26,359,845 (GRCm39) |
missense |
probably benign |
0.20 |
R9546:Notch1
|
UTSW |
2 |
26,371,127 (GRCm39) |
missense |
probably damaging |
0.97 |
R9674:Notch1
|
UTSW |
2 |
26,361,308 (GRCm39) |
missense |
probably damaging |
0.98 |
X0018:Notch1
|
UTSW |
2 |
26,352,239 (GRCm39) |
nonsense |
probably null |
|
X0066:Notch1
|
UTSW |
2 |
26,360,347 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1088:Notch1
|
UTSW |
2 |
26,367,127 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Notch1
|
UTSW |
2 |
26,350,321 (GRCm39) |
missense |
possibly damaging |
0.74 |
|