Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abat |
A |
T |
16: 8,396,100 (GRCm39) |
R19* |
probably null |
Het |
Abcb9 |
A |
G |
5: 124,218,118 (GRCm39) |
M406T |
probably benign |
Het |
Ager |
A |
G |
17: 34,817,157 (GRCm39) |
E32G |
probably damaging |
Het |
Cdk10 |
T |
A |
8: 123,955,579 (GRCm39) |
|
probably null |
Het |
Cfap97d1 |
A |
G |
11: 101,881,640 (GRCm39) |
N112S |
probably damaging |
Het |
Ctsl |
A |
T |
13: 64,514,302 (GRCm39) |
Y259N |
probably damaging |
Het |
Ctu2 |
T |
C |
8: 123,207,965 (GRCm39) |
|
probably null |
Het |
Dse |
T |
A |
10: 34,029,375 (GRCm39) |
I572F |
possibly damaging |
Het |
Flt1 |
A |
T |
5: 147,517,247 (GRCm39) |
|
probably null |
Het |
Gatm |
T |
A |
2: 122,433,083 (GRCm39) |
Y193F |
probably benign |
Het |
Gpaa1 |
T |
C |
15: 76,216,826 (GRCm39) |
F170S |
probably damaging |
Het |
Grm3 |
A |
G |
5: 9,620,155 (GRCm39) |
L363P |
probably benign |
Het |
Heatr5b |
G |
A |
17: 79,138,951 (GRCm39) |
P64S |
probably damaging |
Het |
Hfm1 |
A |
G |
5: 107,026,455 (GRCm39) |
|
probably null |
Het |
Hivep2 |
A |
C |
10: 14,009,519 (GRCm39) |
K1725N |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,550,098 (GRCm39) |
C2695* |
probably null |
Het |
Hmgcr |
G |
A |
13: 96,802,695 (GRCm39) |
T68M |
probably damaging |
Het |
Igsf21 |
A |
T |
4: 139,755,385 (GRCm39) |
D423E |
possibly damaging |
Het |
Klrc2 |
A |
T |
6: 129,637,436 (GRCm39) |
N28K |
possibly damaging |
Het |
Lrrc8c |
A |
T |
5: 105,727,423 (GRCm39) |
D29V |
possibly damaging |
Het |
Mtcl1 |
A |
C |
17: 66,650,132 (GRCm39) |
S1329A |
probably benign |
Het |
Nin |
C |
T |
12: 70,092,375 (GRCm39) |
V645I |
possibly damaging |
Het |
Or4c127 |
T |
C |
2: 89,833,332 (GRCm39) |
I194T |
possibly damaging |
Het |
Or51i1 |
T |
C |
7: 103,671,439 (GRCm39) |
I29V |
probably benign |
Het |
Or8s2 |
T |
A |
15: 98,276,215 (GRCm39) |
M259L |
probably benign |
Het |
Or9g4 |
T |
A |
2: 85,504,682 (GRCm39) |
D271V |
probably damaging |
Het |
Pfpl |
A |
T |
19: 12,407,027 (GRCm39) |
H426L |
probably benign |
Het |
Poteg |
A |
G |
8: 27,946,826 (GRCm39) |
D238G |
probably damaging |
Het |
Psen1 |
T |
C |
12: 83,778,474 (GRCm39) |
F386L |
probably damaging |
Het |
Rassf9 |
A |
T |
10: 102,380,905 (GRCm39) |
I96F |
probably damaging |
Het |
Robo1 |
T |
C |
16: 72,840,077 (GRCm39) |
|
probably null |
Het |
Slc16a4 |
A |
T |
3: 107,206,280 (GRCm39) |
M117L |
probably benign |
Het |
Slc4a8 |
A |
G |
15: 100,689,506 (GRCm39) |
N372S |
possibly damaging |
Het |
Stmn4 |
G |
A |
14: 66,593,748 (GRCm39) |
G47D |
probably benign |
Het |
Tex26 |
A |
G |
5: 149,386,612 (GRCm39) |
N137S |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,747,163 (GRCm39) |
I4629F |
probably benign |
Het |
Ubash3a |
G |
A |
17: 31,427,206 (GRCm39) |
|
probably null |
Het |
Ube3d |
T |
C |
9: 86,307,401 (GRCm39) |
I233V |
probably benign |
Het |
Utrn |
T |
A |
10: 12,297,369 (GRCm39) |
T680S |
probably damaging |
Het |
Vps13d |
G |
A |
4: 144,826,640 (GRCm39) |
T2846I |
probably benign |
Het |
Zbtb22 |
TGGACCCGGGAC |
TGGACCCGGGACCCGGGAC |
17: 34,137,593 (GRCm39) |
|
probably null |
Het |
Zfp41 |
C |
T |
15: 75,490,557 (GRCm39) |
P170S |
probably damaging |
Het |
|
Other mutations in Jag1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Jag1
|
APN |
2 |
136,927,952 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL00912:Jag1
|
APN |
2 |
136,957,493 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01104:Jag1
|
APN |
2 |
136,926,298 (GRCm39) |
missense |
probably benign |
0.40 |
IGL01529:Jag1
|
APN |
2 |
136,926,897 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01578:Jag1
|
APN |
2 |
136,941,971 (GRCm39) |
splice site |
probably benign |
|
IGL01720:Jag1
|
APN |
2 |
136,929,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01809:Jag1
|
APN |
2 |
136,957,404 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02402:Jag1
|
APN |
2 |
136,927,858 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02434:Jag1
|
APN |
2 |
136,929,075 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02543:Jag1
|
APN |
2 |
136,933,867 (GRCm39) |
splice site |
probably benign |
|
IGL02650:Jag1
|
APN |
2 |
136,957,505 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03010:Jag1
|
APN |
2 |
136,935,118 (GRCm39) |
splice site |
probably benign |
|
IGL03102:Jag1
|
APN |
2 |
136,926,608 (GRCm39) |
missense |
probably benign |
0.00 |
Grenville
|
UTSW |
2 |
136,929,062 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4651001:Jag1
|
UTSW |
2 |
136,943,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R0227:Jag1
|
UTSW |
2 |
136,957,538 (GRCm39) |
missense |
probably benign |
|
R0306:Jag1
|
UTSW |
2 |
136,927,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Jag1
|
UTSW |
2 |
136,937,365 (GRCm39) |
critical splice donor site |
probably null |
|
R0594:Jag1
|
UTSW |
2 |
136,929,000 (GRCm39) |
missense |
probably damaging |
0.99 |
R0838:Jag1
|
UTSW |
2 |
136,935,198 (GRCm39) |
missense |
probably damaging |
0.98 |
R0879:Jag1
|
UTSW |
2 |
136,942,001 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0900:Jag1
|
UTSW |
2 |
136,932,802 (GRCm39) |
frame shift |
probably null |
|
R0972:Jag1
|
UTSW |
2 |
136,925,371 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1083:Jag1
|
UTSW |
2 |
136,938,152 (GRCm39) |
missense |
probably damaging |
0.99 |
R1182:Jag1
|
UTSW |
2 |
136,933,409 (GRCm39) |
missense |
probably benign |
0.36 |
R1292:Jag1
|
UTSW |
2 |
136,925,393 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1464:Jag1
|
UTSW |
2 |
136,957,568 (GRCm39) |
missense |
probably damaging |
0.98 |
R1464:Jag1
|
UTSW |
2 |
136,957,568 (GRCm39) |
missense |
probably damaging |
0.98 |
R1500:Jag1
|
UTSW |
2 |
136,957,558 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1936:Jag1
|
UTSW |
2 |
136,925,393 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1937:Jag1
|
UTSW |
2 |
136,925,393 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1939:Jag1
|
UTSW |
2 |
136,925,393 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1998:Jag1
|
UTSW |
2 |
136,932,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Jag1
|
UTSW |
2 |
136,926,599 (GRCm39) |
missense |
probably benign |
0.37 |
R2213:Jag1
|
UTSW |
2 |
136,931,812 (GRCm39) |
missense |
probably benign |
0.01 |
R2300:Jag1
|
UTSW |
2 |
136,938,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R2484:Jag1
|
UTSW |
2 |
136,926,620 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4179:Jag1
|
UTSW |
2 |
136,943,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R4212:Jag1
|
UTSW |
2 |
136,926,990 (GRCm39) |
missense |
probably benign |
|
R4630:Jag1
|
UTSW |
2 |
136,927,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Jag1
|
UTSW |
2 |
136,936,376 (GRCm39) |
missense |
probably benign |
0.11 |
R4705:Jag1
|
UTSW |
2 |
136,938,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R4904:Jag1
|
UTSW |
2 |
136,929,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R5050:Jag1
|
UTSW |
2 |
136,927,074 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5288:Jag1
|
UTSW |
2 |
136,937,464 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5367:Jag1
|
UTSW |
2 |
136,927,014 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5385:Jag1
|
UTSW |
2 |
136,937,464 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5386:Jag1
|
UTSW |
2 |
136,937,464 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5430:Jag1
|
UTSW |
2 |
136,943,626 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5472:Jag1
|
UTSW |
2 |
136,926,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R5755:Jag1
|
UTSW |
2 |
136,930,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R5764:Jag1
|
UTSW |
2 |
136,931,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R6406:Jag1
|
UTSW |
2 |
136,929,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R6503:Jag1
|
UTSW |
2 |
136,943,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R6721:Jag1
|
UTSW |
2 |
136,936,394 (GRCm39) |
missense |
probably benign |
0.00 |
R6826:Jag1
|
UTSW |
2 |
136,958,095 (GRCm39) |
critical splice donor site |
probably null |
|
R7055:Jag1
|
UTSW |
2 |
136,957,409 (GRCm39) |
missense |
probably benign |
0.26 |
R7214:Jag1
|
UTSW |
2 |
136,948,802 (GRCm39) |
missense |
probably benign |
0.00 |
R7359:Jag1
|
UTSW |
2 |
136,926,226 (GRCm39) |
missense |
probably benign |
|
R7422:Jag1
|
UTSW |
2 |
136,926,975 (GRCm39) |
missense |
probably benign |
|
R7919:Jag1
|
UTSW |
2 |
136,930,366 (GRCm39) |
missense |
probably damaging |
0.97 |
R8071:Jag1
|
UTSW |
2 |
136,943,717 (GRCm39) |
missense |
probably benign |
0.01 |
R8768:Jag1
|
UTSW |
2 |
136,932,708 (GRCm39) |
intron |
probably benign |
|
R8768:Jag1
|
UTSW |
2 |
136,943,521 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8898:Jag1
|
UTSW |
2 |
136,935,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R8920:Jag1
|
UTSW |
2 |
136,931,143 (GRCm39) |
missense |
probably benign |
0.05 |
R9060:Jag1
|
UTSW |
2 |
136,931,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R9120:Jag1
|
UTSW |
2 |
136,930,354 (GRCm39) |
missense |
probably benign |
|
R9193:Jag1
|
UTSW |
2 |
136,931,764 (GRCm39) |
missense |
probably null |
0.99 |
R9200:Jag1
|
UTSW |
2 |
136,929,044 (GRCm39) |
missense |
probably benign |
0.04 |
R9241:Jag1
|
UTSW |
2 |
136,926,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R9326:Jag1
|
UTSW |
2 |
136,931,745 (GRCm39) |
missense |
probably benign |
|
R9334:Jag1
|
UTSW |
2 |
136,943,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R9358:Jag1
|
UTSW |
2 |
136,924,948 (GRCm39) |
missense |
probably benign |
0.26 |
R9444:Jag1
|
UTSW |
2 |
136,936,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R9477:Jag1
|
UTSW |
2 |
136,936,409 (GRCm39) |
missense |
probably damaging |
1.00 |
RF016:Jag1
|
UTSW |
2 |
136,938,176 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Jag1
|
UTSW |
2 |
136,927,071 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Jag1
|
UTSW |
2 |
136,926,939 (GRCm39) |
missense |
probably benign |
0.01 |
|