Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatf |
T |
C |
11: 84,402,323 (GRCm39) |
D121G |
probably benign |
Het |
Ccdc168 |
G |
T |
1: 44,100,023 (GRCm39) |
D358E |
probably benign |
Het |
Cilp2 |
A |
T |
8: 70,335,544 (GRCm39) |
S485T |
probably benign |
Het |
Cux1 |
A |
C |
5: 136,315,862 (GRCm39) |
S1059R |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,314,028 (GRCm39) |
D1948G |
probably benign |
Het |
Fyn |
A |
G |
10: 39,398,781 (GRCm39) |
T126A |
probably benign |
Het |
Gm10134 |
C |
T |
2: 28,396,141 (GRCm39) |
S12F |
probably benign |
Het |
Grm7 |
T |
C |
6: 111,472,642 (GRCm39) |
I827T |
possibly damaging |
Het |
H1f4 |
T |
C |
13: 23,805,943 (GRCm39) |
|
probably benign |
Het |
Hacd4 |
T |
A |
4: 88,341,336 (GRCm39) |
|
probably null |
Het |
Helt |
T |
C |
8: 46,745,709 (GRCm39) |
N58S |
probably damaging |
Het |
Jakmip1 |
T |
C |
5: 37,248,543 (GRCm39) |
Y68H |
probably benign |
Het |
Myof |
G |
T |
19: 37,926,375 (GRCm39) |
H1127N |
probably damaging |
Het |
Nbas |
A |
T |
12: 13,412,593 (GRCm39) |
I971L |
probably benign |
Het |
Or4k39 |
C |
T |
2: 111,239,534 (GRCm39) |
T258I |
probably benign |
Het |
Pakap |
G |
A |
4: 57,883,180 (GRCm39) |
R882H |
probably damaging |
Het |
Peg10 |
A |
G |
6: 4,756,102 (GRCm39) |
|
probably benign |
Het |
Pparg |
G |
T |
6: 115,428,005 (GRCm39) |
R164L |
probably damaging |
Het |
Ppp4r3b |
A |
T |
11: 29,150,725 (GRCm39) |
N464Y |
possibly damaging |
Het |
Ric8b |
T |
C |
10: 84,805,888 (GRCm39) |
V333A |
probably benign |
Het |
Sall2 |
G |
A |
14: 52,550,813 (GRCm39) |
S792L |
probably damaging |
Het |
Slc5a4b |
C |
A |
10: 75,944,383 (GRCm39) |
L87F |
probably damaging |
Het |
Sox12 |
A |
G |
2: 152,238,958 (GRCm39) |
S221P |
possibly damaging |
Het |
Tpr |
T |
A |
1: 150,289,525 (GRCm39) |
S619T |
probably benign |
Het |
Trdmt1 |
G |
A |
2: 13,524,871 (GRCm39) |
Q195* |
probably null |
Het |
Trpm2 |
A |
T |
10: 77,750,640 (GRCm39) |
|
probably benign |
Het |
Ttc3 |
C |
T |
16: 94,232,857 (GRCm39) |
P1003L |
probably damaging |
Het |
Vmn2r112 |
T |
A |
17: 22,822,096 (GRCm39) |
V258E |
probably damaging |
Het |
Zfp318 |
C |
T |
17: 46,710,389 (GRCm39) |
T704I |
probably benign |
Het |
|
Other mutations in Upf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01065:Upf2
|
APN |
2 |
5,966,111 (GRCm39) |
missense |
unknown |
|
IGL01394:Upf2
|
APN |
2 |
6,045,024 (GRCm39) |
splice site |
probably null |
|
IGL01571:Upf2
|
APN |
2 |
6,023,750 (GRCm39) |
unclassified |
probably benign |
|
IGL01624:Upf2
|
APN |
2 |
6,038,990 (GRCm39) |
missense |
probably benign |
|
IGL02121:Upf2
|
APN |
2 |
6,031,134 (GRCm39) |
splice site |
probably benign |
|
IGL02485:Upf2
|
APN |
2 |
6,032,102 (GRCm39) |
missense |
unknown |
|
IGL02491:Upf2
|
APN |
2 |
6,030,975 (GRCm39) |
missense |
unknown |
|
Balderdash
|
UTSW |
2 |
5,978,347 (GRCm39) |
missense |
unknown |
|
nonsense
|
UTSW |
2 |
6,051,845 (GRCm39) |
missense |
unknown |
|
R0265:Upf2
|
UTSW |
2 |
6,032,015 (GRCm39) |
splice site |
probably benign |
|
R0390:Upf2
|
UTSW |
2 |
6,023,705 (GRCm39) |
unclassified |
probably benign |
|
R0480:Upf2
|
UTSW |
2 |
5,962,445 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0513:Upf2
|
UTSW |
2 |
5,962,478 (GRCm39) |
missense |
unknown |
|
R0579:Upf2
|
UTSW |
2 |
5,993,240 (GRCm39) |
missense |
unknown |
|
R0612:Upf2
|
UTSW |
2 |
6,038,909 (GRCm39) |
splice site |
probably benign |
|
R0856:Upf2
|
UTSW |
2 |
5,962,463 (GRCm39) |
missense |
unknown |
|
R1103:Upf2
|
UTSW |
2 |
6,030,986 (GRCm39) |
missense |
unknown |
|
R1384:Upf2
|
UTSW |
2 |
5,965,800 (GRCm39) |
missense |
unknown |
|
R1672:Upf2
|
UTSW |
2 |
6,044,908 (GRCm39) |
splice site |
probably null |
|
R1728:Upf2
|
UTSW |
2 |
6,032,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Upf2
|
UTSW |
2 |
6,032,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Upf2
|
UTSW |
2 |
6,055,135 (GRCm39) |
splice site |
probably null |
|
R2252:Upf2
|
UTSW |
2 |
5,966,271 (GRCm39) |
missense |
unknown |
|
R3015:Upf2
|
UTSW |
2 |
5,980,890 (GRCm39) |
missense |
unknown |
|
R3931:Upf2
|
UTSW |
2 |
6,051,821 (GRCm39) |
missense |
unknown |
|
R4151:Upf2
|
UTSW |
2 |
5,966,516 (GRCm39) |
missense |
unknown |
|
R4283:Upf2
|
UTSW |
2 |
5,978,369 (GRCm39) |
missense |
unknown |
|
R4558:Upf2
|
UTSW |
2 |
5,978,404 (GRCm39) |
missense |
unknown |
|
R4564:Upf2
|
UTSW |
2 |
6,032,123 (GRCm39) |
missense |
unknown |
|
R5630:Upf2
|
UTSW |
2 |
6,032,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R6370:Upf2
|
UTSW |
2 |
5,980,821 (GRCm39) |
missense |
unknown |
|
R6418:Upf2
|
UTSW |
2 |
6,032,150 (GRCm39) |
missense |
unknown |
|
R6432:Upf2
|
UTSW |
2 |
5,984,588 (GRCm39) |
missense |
unknown |
|
R7184:Upf2
|
UTSW |
2 |
6,028,131 (GRCm39) |
missense |
unknown |
|
R7308:Upf2
|
UTSW |
2 |
5,978,329 (GRCm39) |
missense |
unknown |
|
R7371:Upf2
|
UTSW |
2 |
5,965,851 (GRCm39) |
missense |
unknown |
|
R7404:Upf2
|
UTSW |
2 |
6,045,014 (GRCm39) |
missense |
unknown |
|
R7439:Upf2
|
UTSW |
2 |
6,023,743 (GRCm39) |
missense |
unknown |
|
R7441:Upf2
|
UTSW |
2 |
6,023,743 (GRCm39) |
missense |
unknown |
|
R7461:Upf2
|
UTSW |
2 |
5,978,347 (GRCm39) |
missense |
unknown |
|
R7483:Upf2
|
UTSW |
2 |
6,032,219 (GRCm39) |
missense |
unknown |
|
R7613:Upf2
|
UTSW |
2 |
5,978,347 (GRCm39) |
missense |
unknown |
|
R7976:Upf2
|
UTSW |
2 |
6,030,926 (GRCm39) |
missense |
unknown |
|
R8044:Upf2
|
UTSW |
2 |
6,034,249 (GRCm39) |
missense |
unknown |
|
R8516:Upf2
|
UTSW |
2 |
6,023,782 (GRCm39) |
missense |
unknown |
|
R8880:Upf2
|
UTSW |
2 |
6,030,983 (GRCm39) |
missense |
unknown |
|
R8911:Upf2
|
UTSW |
2 |
5,987,893 (GRCm39) |
missense |
unknown |
|
R9138:Upf2
|
UTSW |
2 |
6,028,132 (GRCm39) |
missense |
unknown |
|
R9226:Upf2
|
UTSW |
2 |
6,051,845 (GRCm39) |
missense |
unknown |
|
R9444:Upf2
|
UTSW |
2 |
6,023,755 (GRCm39) |
missense |
unknown |
|
R9484:Upf2
|
UTSW |
2 |
5,966,078 (GRCm39) |
missense |
unknown |
|
R9665:Upf2
|
UTSW |
2 |
6,051,715 (GRCm39) |
missense |
unknown |
|
R9691:Upf2
|
UTSW |
2 |
6,032,024 (GRCm39) |
missense |
unknown |
|
Z1176:Upf2
|
UTSW |
2 |
6,028,199 (GRCm39) |
missense |
unknown |
|
|