Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
A |
6: 121,625,125 (GRCm39) |
F501Y |
probably damaging |
Het |
Ankrd12 |
G |
T |
17: 66,291,000 (GRCm39) |
P1478T |
probably benign |
Het |
Arhgap39 |
A |
G |
15: 76,636,088 (GRCm39) |
V49A |
probably benign |
Het |
Arid4b |
T |
C |
13: 14,307,069 (GRCm39) |
L108P |
probably damaging |
Het |
Atrn |
T |
A |
2: 130,836,127 (GRCm39) |
C1136S |
probably damaging |
Het |
Cacna1s |
T |
A |
1: 136,012,007 (GRCm39) |
M483K |
probably damaging |
Het |
Cacng1 |
C |
A |
11: 107,607,118 (GRCm39) |
V34L |
probably benign |
Het |
Casp8 |
T |
C |
1: 58,883,970 (GRCm39) |
S446P |
probably damaging |
Het |
Cngb3 |
G |
A |
4: 19,461,679 (GRCm39) |
C520Y |
probably damaging |
Het |
Crim1 |
C |
T |
17: 78,588,668 (GRCm39) |
|
probably benign |
Het |
F11 |
A |
G |
8: 45,701,675 (GRCm39) |
S353P |
probably damaging |
Het |
Fbxl17 |
G |
A |
17: 63,806,802 (GRCm39) |
P71S |
possibly damaging |
Het |
Fn1 |
C |
T |
1: 71,647,072 (GRCm39) |
G1482R |
probably damaging |
Het |
Gbp3 |
C |
T |
3: 142,272,099 (GRCm39) |
|
probably benign |
Het |
Golga4 |
A |
G |
9: 118,387,804 (GRCm39) |
D1642G |
possibly damaging |
Het |
Hspa1a |
C |
T |
17: 35,190,703 (GRCm39) |
V67M |
probably damaging |
Het |
Hyls1 |
T |
C |
9: 35,472,705 (GRCm39) |
D237G |
probably damaging |
Het |
Kmt2e |
A |
G |
5: 23,706,624 (GRCm39) |
N1396D |
probably benign |
Het |
Lasp1 |
G |
A |
11: 97,690,653 (GRCm39) |
V12M |
probably damaging |
Het |
Muc4 |
G |
C |
16: 32,753,919 (GRCm38) |
R1265P |
probably benign |
Het |
Muc5b |
C |
T |
7: 141,403,235 (GRCm39) |
T732M |
unknown |
Het |
Mxd1 |
G |
T |
6: 86,627,942 (GRCm39) |
Q199K |
probably benign |
Het |
Or14a258 |
T |
A |
7: 86,035,182 (GRCm39) |
T229S |
probably benign |
Het |
Or4a78 |
T |
C |
2: 89,497,357 (GRCm39) |
E291G |
probably damaging |
Het |
Or5w18 |
T |
A |
2: 87,633,031 (GRCm39) |
F95L |
probably benign |
Het |
Or5w20 |
T |
A |
2: 87,727,293 (GRCm39) |
|
probably null |
Het |
Prps1l1 |
A |
T |
12: 35,035,797 (GRCm39) |
H304L |
possibly damaging |
Het |
Psmd2 |
A |
G |
16: 20,474,392 (GRCm39) |
D316G |
probably benign |
Het |
Rlf |
G |
A |
4: 121,006,229 (GRCm39) |
T917I |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,466,953 (GRCm39) |
D4704G |
probably damaging |
Het |
Scn1a |
T |
A |
2: 66,104,332 (GRCm39) |
I1643F |
probably damaging |
Het |
Vmn2r38 |
T |
C |
7: 9,078,553 (GRCm39) |
K610E |
probably damaging |
Het |
Zfc3h1 |
T |
C |
10: 115,255,806 (GRCm39) |
F1486L |
probably benign |
Het |
|
Other mutations in Alk |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00401:Alk
|
APN |
17 |
72,202,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00796:Alk
|
APN |
17 |
72,212,137 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01096:Alk
|
APN |
17 |
72,228,891 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01367:Alk
|
APN |
17 |
72,207,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01402:Alk
|
APN |
17 |
72,181,173 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01652:Alk
|
APN |
17 |
72,910,526 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01717:Alk
|
APN |
17 |
72,910,377 (GRCm39) |
missense |
probably benign |
|
IGL02301:Alk
|
APN |
17 |
72,181,171 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02403:Alk
|
APN |
17 |
72,208,388 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02452:Alk
|
APN |
17 |
72,209,620 (GRCm39) |
nonsense |
probably null |
|
IGL02724:Alk
|
APN |
17 |
72,292,455 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02826:Alk
|
APN |
17 |
72,176,531 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02863:Alk
|
APN |
17 |
72,204,830 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02994:Alk
|
APN |
17 |
72,256,815 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03329:Alk
|
APN |
17 |
72,206,159 (GRCm39) |
splice site |
probably benign |
|
PIT4382001:Alk
|
UTSW |
17 |
72,256,916 (GRCm39) |
missense |
probably benign |
|
R0157:Alk
|
UTSW |
17 |
72,256,840 (GRCm39) |
missense |
probably benign |
0.00 |
R0211:Alk
|
UTSW |
17 |
72,910,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R0257:Alk
|
UTSW |
17 |
72,910,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R0269:Alk
|
UTSW |
17 |
72,910,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R0395:Alk
|
UTSW |
17 |
72,910,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R0414:Alk
|
UTSW |
17 |
72,206,281 (GRCm39) |
splice site |
probably benign |
|
R0466:Alk
|
UTSW |
17 |
72,212,152 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0526:Alk
|
UTSW |
17 |
72,176,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Alk
|
UTSW |
17 |
72,910,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Alk
|
UTSW |
17 |
72,291,740 (GRCm39) |
splice site |
probably benign |
|
R0830:Alk
|
UTSW |
17 |
72,910,195 (GRCm39) |
missense |
probably benign |
0.01 |
R0835:Alk
|
UTSW |
17 |
72,176,837 (GRCm39) |
missense |
probably damaging |
0.97 |
R0894:Alk
|
UTSW |
17 |
72,202,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Alk
|
UTSW |
17 |
72,291,740 (GRCm39) |
splice site |
probably benign |
|
R1170:Alk
|
UTSW |
17 |
72,207,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1573:Alk
|
UTSW |
17 |
72,910,113 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1667:Alk
|
UTSW |
17 |
72,218,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R1748:Alk
|
UTSW |
17 |
72,910,416 (GRCm39) |
missense |
probably benign |
0.19 |
R1767:Alk
|
UTSW |
17 |
72,207,693 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1836:Alk
|
UTSW |
17 |
72,198,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R1861:Alk
|
UTSW |
17 |
72,181,933 (GRCm39) |
splice site |
probably benign |
|
R2905:Alk
|
UTSW |
17 |
72,292,489 (GRCm39) |
missense |
probably benign |
0.40 |
R2925:Alk
|
UTSW |
17 |
72,910,202 (GRCm39) |
missense |
probably benign |
|
R3727:Alk
|
UTSW |
17 |
72,208,395 (GRCm39) |
splice site |
probably benign |
|
R3747:Alk
|
UTSW |
17 |
72,218,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R3790:Alk
|
UTSW |
17 |
72,910,427 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3934:Alk
|
UTSW |
17 |
72,512,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R3936:Alk
|
UTSW |
17 |
72,512,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R3972:Alk
|
UTSW |
17 |
72,292,442 (GRCm39) |
missense |
probably benign |
0.16 |
R4433:Alk
|
UTSW |
17 |
72,206,236 (GRCm39) |
nonsense |
probably null |
|
R4716:Alk
|
UTSW |
17 |
72,512,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R4903:Alk
|
UTSW |
17 |
72,176,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Alk
|
UTSW |
17 |
72,211,310 (GRCm39) |
missense |
probably benign |
0.30 |
R4954:Alk
|
UTSW |
17 |
72,209,687 (GRCm39) |
nonsense |
probably null |
|
R5377:Alk
|
UTSW |
17 |
72,202,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R5386:Alk
|
UTSW |
17 |
72,182,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5551:Alk
|
UTSW |
17 |
72,182,028 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5704:Alk
|
UTSW |
17 |
72,910,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R5877:Alk
|
UTSW |
17 |
72,274,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5888:Alk
|
UTSW |
17 |
72,181,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R6013:Alk
|
UTSW |
17 |
72,207,732 (GRCm39) |
missense |
probably benign |
0.15 |
R6044:Alk
|
UTSW |
17 |
72,299,095 (GRCm39) |
missense |
probably benign |
0.00 |
R6058:Alk
|
UTSW |
17 |
72,176,742 (GRCm39) |
missense |
probably benign |
0.01 |
R6126:Alk
|
UTSW |
17 |
72,182,037 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6286:Alk
|
UTSW |
17 |
72,187,842 (GRCm39) |
missense |
probably damaging |
0.98 |
R6744:Alk
|
UTSW |
17 |
72,910,077 (GRCm39) |
missense |
probably benign |
0.35 |
R6989:Alk
|
UTSW |
17 |
72,204,947 (GRCm39) |
missense |
probably benign |
0.00 |
R7487:Alk
|
UTSW |
17 |
72,256,893 (GRCm39) |
missense |
probably benign |
|
R7573:Alk
|
UTSW |
17 |
72,207,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R7838:Alk
|
UTSW |
17 |
72,274,549 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8055:Alk
|
UTSW |
17 |
72,206,252 (GRCm39) |
missense |
probably benign |
0.19 |
R8211:Alk
|
UTSW |
17 |
72,176,702 (GRCm39) |
missense |
probably benign |
|
R8555:Alk
|
UTSW |
17 |
72,228,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R8676:Alk
|
UTSW |
17 |
72,204,936 (GRCm39) |
missense |
probably damaging |
0.98 |
R8847:Alk
|
UTSW |
17 |
72,256,820 (GRCm39) |
missense |
probably benign |
0.14 |
R8885:Alk
|
UTSW |
17 |
72,202,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R9177:Alk
|
UTSW |
17 |
72,181,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R9239:Alk
|
UTSW |
17 |
72,256,864 (GRCm39) |
missense |
probably benign |
0.04 |
R9268:Alk
|
UTSW |
17 |
72,181,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R9682:Alk
|
UTSW |
17 |
72,182,058 (GRCm39) |
missense |
possibly damaging |
0.95 |
RF013:Alk
|
UTSW |
17 |
72,202,931 (GRCm39) |
missense |
probably damaging |
1.00 |
RF018:Alk
|
UTSW |
17 |
72,256,808 (GRCm39) |
missense |
probably benign |
0.09 |
Z1088:Alk
|
UTSW |
17 |
72,512,802 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Alk
|
UTSW |
17 |
72,910,058 (GRCm39) |
missense |
probably damaging |
0.97 |
|