Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
C |
A |
1: 12,042,300 (GRCm39) |
S440* |
probably null |
Het |
Abl2 |
T |
A |
1: 156,469,133 (GRCm39) |
M695K |
probably damaging |
Het |
Asap2 |
T |
C |
12: 21,279,482 (GRCm39) |
I426T |
probably damaging |
Het |
Atxn7l1 |
T |
C |
12: 33,391,991 (GRCm39) |
M93T |
probably damaging |
Het |
Ccr5 |
T |
C |
9: 123,925,111 (GRCm39) |
L238P |
possibly damaging |
Het |
Cd27 |
A |
G |
6: 125,211,633 (GRCm39) |
V98A |
probably benign |
Het |
Ceacam23 |
T |
A |
7: 17,639,118 (GRCm39) |
Y372N |
probably benign |
Het |
Cfap47 |
C |
G |
X: 78,541,635 (GRCm39) |
K469N |
probably damaging |
Het |
Chrdl2 |
A |
G |
7: 99,671,229 (GRCm39) |
T116A |
probably damaging |
Het |
Epha6 |
T |
C |
16: 60,346,883 (GRCm39) |
|
probably null |
Het |
Garin1b |
A |
G |
6: 29,326,611 (GRCm39) |
S243G |
probably damaging |
Het |
Gart |
T |
C |
16: 91,430,880 (GRCm39) |
E394G |
possibly damaging |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Lpar6 |
G |
A |
14: 73,476,381 (GRCm39) |
R114Q |
probably damaging |
Het |
Med23 |
G |
T |
10: 24,780,168 (GRCm39) |
E573* |
probably null |
Het |
Mtch2 |
A |
G |
2: 90,689,827 (GRCm39) |
I183V |
probably benign |
Het |
Nlrp3 |
C |
T |
11: 59,438,836 (GRCm39) |
R138* |
probably null |
Het |
Or4k37 |
A |
G |
2: 111,159,643 (GRCm39) |
D293G |
probably null |
Het |
Rbm20 |
A |
G |
19: 53,831,691 (GRCm39) |
S642G |
probably damaging |
Het |
Tex11 |
C |
A |
X: 99,977,021 (GRCm39) |
A487S |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,748,681 (GRCm39) |
S4123G |
probably benign |
Het |
Ugt3a1 |
A |
C |
15: 9,306,360 (GRCm39) |
S170R |
possibly damaging |
Het |
Vmn2r71 |
G |
T |
7: 85,273,360 (GRCm39) |
D725Y |
probably damaging |
Het |
Vps9d1 |
G |
T |
8: 123,974,976 (GRCm39) |
|
probably benign |
Het |
Yeats2 |
A |
G |
16: 20,027,172 (GRCm39) |
T808A |
probably damaging |
Het |
Zdhhc4 |
C |
T |
5: 143,310,099 (GRCm39) |
|
probably benign |
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 |
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 |
|
R4989:Notch1
|
UTSW |
2 |
26,371,193 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|