Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
C |
T |
6: 128,557,349 (GRCm39) |
A115T |
probably benign |
Het |
Abca13 |
A |
G |
11: 9,206,185 (GRCm39) |
T162A |
possibly damaging |
Het |
Adamts9 |
T |
A |
6: 92,837,184 (GRCm39) |
D578V |
probably damaging |
Het |
Atp6v1a |
T |
C |
16: 43,927,403 (GRCm39) |
T295A |
probably benign |
Het |
Brinp1 |
A |
G |
4: 68,681,184 (GRCm39) |
S449P |
probably damaging |
Het |
Ccdc40 |
A |
G |
11: 119,153,943 (GRCm39) |
T1072A |
probably benign |
Het |
Chil4 |
C |
A |
3: 106,121,616 (GRCm39) |
E78* |
probably null |
Het |
Dock3 |
T |
C |
9: 106,829,554 (GRCm39) |
D1120G |
probably damaging |
Het |
Gfod1 |
A |
G |
13: 43,354,621 (GRCm39) |
M118T |
probably benign |
Het |
Ints5 |
A |
G |
19: 8,874,143 (GRCm39) |
T701A |
probably benign |
Het |
Map4k2 |
G |
T |
19: 6,391,958 (GRCm39) |
E91* |
probably null |
Het |
Mast4 |
T |
A |
13: 102,910,695 (GRCm39) |
E457D |
probably damaging |
Het |
Mettl4 |
T |
C |
17: 95,040,576 (GRCm39) |
D404G |
probably damaging |
Het |
Mgat4a |
A |
G |
1: 37,503,614 (GRCm39) |
F58L |
probably damaging |
Het |
Myh4 |
A |
G |
11: 67,146,454 (GRCm39) |
K1476E |
probably damaging |
Het |
Myl7 |
T |
C |
11: 5,846,684 (GRCm39) |
E175G |
probably damaging |
Het |
Myo18a |
A |
G |
11: 77,668,596 (GRCm39) |
E152G |
probably benign |
Het |
Ncan |
G |
A |
8: 70,565,463 (GRCm39) |
T187I |
probably benign |
Het |
Nfatc3 |
A |
G |
8: 106,835,087 (GRCm39) |
Y803C |
probably damaging |
Het |
Nlrp4f |
T |
C |
13: 65,338,660 (GRCm39) |
Y659C |
probably damaging |
Het |
Noxred1 |
T |
C |
12: 87,273,820 (GRCm39) |
T74A |
probably benign |
Het |
Ntrk2 |
A |
T |
13: 59,202,248 (GRCm39) |
M619L |
probably benign |
Het |
Or5w18 |
A |
T |
2: 87,633,159 (GRCm39) |
N142I |
probably benign |
Het |
Orc4 |
A |
G |
2: 48,823,111 (GRCm39) |
V120A |
probably benign |
Het |
Polq |
T |
A |
16: 36,894,301 (GRCm39) |
Y2037N |
probably damaging |
Het |
Rimbp2 |
A |
G |
5: 128,880,908 (GRCm39) |
C160R |
probably damaging |
Het |
Rps6ka4 |
T |
C |
19: 6,807,468 (GRCm39) |
S721G |
possibly damaging |
Het |
Skap2 |
C |
T |
6: 51,898,310 (GRCm39) |
R140Q |
probably damaging |
Het |
Srprb |
C |
T |
9: 103,074,755 (GRCm39) |
R838H |
probably damaging |
Het |
|
Other mutations in Cul7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00557:Cul7
|
APN |
17 |
46,963,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01288:Cul7
|
APN |
17 |
46,968,733 (GRCm39) |
splice site |
probably benign |
|
IGL01669:Cul7
|
APN |
17 |
46,969,641 (GRCm39) |
missense |
possibly damaging |
0.94 |
P0019:Cul7
|
UTSW |
17 |
46,971,173 (GRCm39) |
splice site |
probably benign |
|
PIT4453001:Cul7
|
UTSW |
17 |
46,962,746 (GRCm39) |
missense |
probably damaging |
0.99 |
R0083:Cul7
|
UTSW |
17 |
46,966,482 (GRCm39) |
missense |
probably benign |
0.00 |
R0121:Cul7
|
UTSW |
17 |
46,974,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R0157:Cul7
|
UTSW |
17 |
46,964,761 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0266:Cul7
|
UTSW |
17 |
46,965,521 (GRCm39) |
missense |
probably benign |
0.00 |
R0358:Cul7
|
UTSW |
17 |
46,974,670 (GRCm39) |
critical splice donor site |
probably null |
|
R0544:Cul7
|
UTSW |
17 |
46,974,470 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0565:Cul7
|
UTSW |
17 |
46,962,929 (GRCm39) |
missense |
probably damaging |
0.98 |
R0677:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R0696:Cul7
|
UTSW |
17 |
46,970,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R0702:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R0735:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R0893:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R0900:Cul7
|
UTSW |
17 |
46,969,263 (GRCm39) |
missense |
probably benign |
0.36 |
R0975:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R0976:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R1014:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R1016:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R1104:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R1162:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R1378:Cul7
|
UTSW |
17 |
46,973,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R1479:Cul7
|
UTSW |
17 |
46,962,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R1498:Cul7
|
UTSW |
17 |
46,966,636 (GRCm39) |
missense |
probably benign |
0.01 |
R1521:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R1542:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R1545:Cul7
|
UTSW |
17 |
46,962,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R1598:Cul7
|
UTSW |
17 |
46,974,017 (GRCm39) |
missense |
probably benign |
0.10 |
R1600:Cul7
|
UTSW |
17 |
46,962,748 (GRCm39) |
nonsense |
probably null |
|
R1618:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R1752:Cul7
|
UTSW |
17 |
46,964,093 (GRCm39) |
missense |
probably benign |
0.10 |
R1881:Cul7
|
UTSW |
17 |
46,962,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R1901:Cul7
|
UTSW |
17 |
46,966,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1902:Cul7
|
UTSW |
17 |
46,966,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1913:Cul7
|
UTSW |
17 |
46,974,116 (GRCm39) |
missense |
probably damaging |
0.99 |
R2213:Cul7
|
UTSW |
17 |
46,962,398 (GRCm39) |
missense |
probably damaging |
0.99 |
R2929:Cul7
|
UTSW |
17 |
46,962,526 (GRCm39) |
missense |
probably benign |
0.00 |
R2930:Cul7
|
UTSW |
17 |
46,962,526 (GRCm39) |
missense |
probably benign |
0.00 |
R2990:Cul7
|
UTSW |
17 |
46,962,526 (GRCm39) |
missense |
probably benign |
0.00 |
R2992:Cul7
|
UTSW |
17 |
46,962,526 (GRCm39) |
missense |
probably benign |
0.00 |
R4201:Cul7
|
UTSW |
17 |
46,972,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R4792:Cul7
|
UTSW |
17 |
46,967,976 (GRCm39) |
nonsense |
probably null |
|
R4971:Cul7
|
UTSW |
17 |
46,970,045 (GRCm39) |
missense |
probably benign |
0.00 |
R5014:Cul7
|
UTSW |
17 |
46,966,868 (GRCm39) |
makesense |
probably null |
|
R5384:Cul7
|
UTSW |
17 |
46,965,403 (GRCm39) |
missense |
probably benign |
0.44 |
R5957:Cul7
|
UTSW |
17 |
46,968,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R6128:Cul7
|
UTSW |
17 |
46,962,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R6294:Cul7
|
UTSW |
17 |
46,974,074 (GRCm39) |
missense |
probably benign |
|
R6812:Cul7
|
UTSW |
17 |
46,972,335 (GRCm39) |
missense |
probably benign |
0.00 |
R7073:Cul7
|
UTSW |
17 |
46,969,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R7112:Cul7
|
UTSW |
17 |
46,962,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R7246:Cul7
|
UTSW |
17 |
46,972,993 (GRCm39) |
missense |
probably benign |
0.04 |
R7361:Cul7
|
UTSW |
17 |
46,967,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7567:Cul7
|
UTSW |
17 |
46,965,521 (GRCm39) |
missense |
probably benign |
0.00 |
R7682:Cul7
|
UTSW |
17 |
46,966,521 (GRCm39) |
missense |
probably benign |
|
R7689:Cul7
|
UTSW |
17 |
46,963,747 (GRCm39) |
nonsense |
probably null |
|
R7797:Cul7
|
UTSW |
17 |
46,969,568 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7897:Cul7
|
UTSW |
17 |
46,968,931 (GRCm39) |
missense |
probably benign |
|
R8783:Cul7
|
UTSW |
17 |
46,966,575 (GRCm39) |
missense |
probably benign |
|
R9047:Cul7
|
UTSW |
17 |
46,965,448 (GRCm39) |
missense |
probably benign |
0.01 |
R9167:Cul7
|
UTSW |
17 |
46,966,623 (GRCm39) |
missense |
probably benign |
0.14 |
R9614:Cul7
|
UTSW |
17 |
46,975,212 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cul7
|
UTSW |
17 |
46,970,495 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Cul7
|
UTSW |
17 |
46,969,664 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Cul7
|
UTSW |
17 |
46,963,731 (GRCm39) |
frame shift |
probably null |
|
|