Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl1 |
G |
T |
8: 84,656,746 (GRCm39) |
E355* |
probably null |
Het |
Aldh6a1 |
G |
T |
12: 84,486,303 (GRCm39) |
T205N |
probably damaging |
Het |
Arhgap24 |
A |
G |
5: 103,008,291 (GRCm39) |
I71V |
probably damaging |
Het |
Arid2 |
A |
T |
15: 96,299,887 (GRCm39) |
E1800V |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Cd53 |
T |
C |
3: 106,670,572 (GRCm39) |
T154A |
probably benign |
Het |
Chd7 |
G |
A |
4: 8,855,241 (GRCm39) |
A2157T |
probably benign |
Het |
Clca4b |
A |
T |
3: 144,622,432 (GRCm39) |
N544K |
probably benign |
Het |
Cntrl |
A |
G |
2: 35,017,525 (GRCm39) |
E444G |
probably benign |
Het |
Crygs |
C |
T |
16: 22,624,301 (GRCm39) |
G102D |
possibly damaging |
Het |
Gabrr1 |
A |
G |
4: 33,152,449 (GRCm39) |
K130E |
probably benign |
Het |
H3f3a |
C |
T |
1: 180,630,703 (GRCm39) |
R117H |
probably benign |
Het |
Kif11 |
A |
G |
19: 37,399,987 (GRCm39) |
T825A |
probably benign |
Het |
Lama4 |
T |
A |
10: 38,963,316 (GRCm39) |
M1296K |
probably benign |
Het |
Lrp1 |
G |
T |
10: 127,392,784 (GRCm39) |
C2760* |
probably null |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Nolc1 |
CAG |
CAGAAG |
19: 46,069,798 (GRCm39) |
|
probably benign |
Het |
Nolc1 |
CAG |
CAGTAG |
19: 46,069,807 (GRCm39) |
|
probably benign |
Het |
Nop16 |
A |
G |
13: 54,733,679 (GRCm39) |
|
probably null |
Het |
Or2n1 |
T |
A |
17: 38,486,441 (GRCm39) |
Y155* |
probably null |
Het |
Or5ak22 |
T |
C |
2: 85,230,476 (GRCm39) |
I134V |
probably benign |
Het |
Ostf1 |
T |
C |
19: 18,558,644 (GRCm39) |
D213G |
probably damaging |
Het |
Slc28a2 |
C |
T |
2: 122,272,259 (GRCm39) |
Q34* |
probably null |
Het |
St18 |
A |
G |
1: 6,925,626 (GRCm39) |
D928G |
probably damaging |
Het |
Stag1 |
T |
C |
9: 100,594,553 (GRCm39) |
V31A |
possibly damaging |
Het |
Tcl1b1 |
G |
A |
12: 105,130,783 (GRCm39) |
A89T |
probably benign |
Het |
Tsen54 |
A |
T |
11: 115,712,904 (GRCm39) |
S464C |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,737,792 (GRCm39) |
F4249S |
probably benign |
Het |
Xdh |
A |
G |
17: 74,198,260 (GRCm39) |
F1209S |
probably damaging |
Het |
Ylpm1 |
G |
A |
12: 85,107,093 (GRCm39) |
|
probably null |
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 |
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 |
R5804:Jag1
|
UTSW |
2 |
136,930,124 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
|