Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts17 |
T |
C |
7: 66,559,124 (GRCm39) |
F305L |
probably damaging |
Het |
Bloc1s5 |
A |
T |
13: 38,787,859 (GRCm39) |
M175K |
probably damaging |
Het |
C9 |
T |
A |
15: 6,526,613 (GRCm39) |
M549K |
probably benign |
Het |
Cfap52 |
A |
G |
11: 67,845,007 (GRCm39) |
|
probably benign |
Het |
Cntnap2 |
A |
T |
6: 46,998,670 (GRCm39) |
K907N |
possibly damaging |
Het |
Cox8c |
T |
A |
12: 102,865,752 (GRCm39) |
|
probably null |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Cyp26b1 |
A |
T |
6: 84,551,294 (GRCm39) |
N307K |
possibly damaging |
Het |
Cyp2s1 |
T |
C |
7: 25,515,849 (GRCm39) |
|
probably benign |
Het |
Dpysl2 |
G |
A |
14: 67,061,847 (GRCm39) |
T253I |
probably damaging |
Het |
Efr3b |
C |
T |
12: 4,033,391 (GRCm39) |
V139I |
probably benign |
Het |
Egflam |
T |
A |
15: 7,252,293 (GRCm39) |
I835F |
probably damaging |
Het |
Eif5a |
A |
T |
11: 69,809,989 (GRCm39) |
H51Q |
possibly damaging |
Het |
Fancd2 |
T |
A |
6: 113,539,422 (GRCm39) |
I637N |
probably damaging |
Het |
Gpr173 |
T |
A |
X: 151,130,092 (GRCm39) |
H127L |
probably damaging |
Het |
Klc3 |
T |
C |
7: 19,130,969 (GRCm39) |
I203V |
probably benign |
Het |
Lsg1 |
T |
C |
16: 30,390,060 (GRCm39) |
K352E |
probably benign |
Het |
Man2a2 |
G |
A |
7: 80,009,388 (GRCm39) |
A822V |
probably damaging |
Het |
Med12l |
G |
T |
3: 58,984,510 (GRCm39) |
D483Y |
probably damaging |
Het |
Mlh1 |
A |
G |
9: 111,058,943 (GRCm39) |
Y694H |
probably benign |
Het |
Mmrn1 |
A |
G |
6: 60,935,160 (GRCm39) |
R219G |
possibly damaging |
Het |
Nsd1 |
T |
C |
13: 55,450,646 (GRCm39) |
|
probably benign |
Het |
Or2y1f |
A |
T |
11: 49,184,555 (GRCm39) |
M136L |
possibly damaging |
Het |
Or8k33 |
C |
T |
2: 86,384,224 (GRCm39) |
M81I |
possibly damaging |
Het |
Pax3 |
A |
T |
1: 78,098,424 (GRCm39) |
S322T |
possibly damaging |
Het |
Pkhd1 |
T |
A |
1: 20,187,944 (GRCm39) |
I3455F |
probably damaging |
Het |
Plekhb2 |
T |
C |
1: 34,916,022 (GRCm39) |
V187A |
possibly damaging |
Het |
Pot1a |
A |
T |
6: 25,794,592 (GRCm39) |
F31I |
probably damaging |
Het |
Rpap1 |
A |
T |
2: 119,613,720 (GRCm39) |
|
probably benign |
Het |
Scmh1 |
T |
A |
4: 120,385,343 (GRCm39) |
|
probably benign |
Het |
Scn2a |
A |
G |
2: 65,560,522 (GRCm39) |
T1251A |
probably damaging |
Het |
Siglecf |
T |
C |
7: 43,001,634 (GRCm39) |
V148A |
probably benign |
Het |
Slit3 |
A |
G |
11: 35,598,969 (GRCm39) |
*1524W |
probably null |
Het |
Son |
C |
A |
16: 91,455,359 (GRCm39) |
P1369T |
possibly damaging |
Het |
Spp2 |
T |
A |
1: 88,338,868 (GRCm39) |
L25* |
probably null |
Het |
Sptbn4 |
T |
C |
7: 27,090,976 (GRCm39) |
Q1405R |
probably damaging |
Het |
Traf3ip2 |
G |
T |
10: 39,522,902 (GRCm39) |
A463S |
possibly damaging |
Het |
Trappc11 |
T |
C |
8: 47,960,617 (GRCm39) |
E27G |
probably damaging |
Het |
Vmn2r12 |
C |
T |
5: 109,233,858 (GRCm39) |
V785I |
probably damaging |
Het |
Zc3h8 |
A |
G |
2: 128,785,846 (GRCm39) |
|
probably benign |
Het |
Zfp57 |
T |
A |
17: 37,317,056 (GRCm39) |
S45T |
probably damaging |
Het |
|
Other mutations in Ankrd12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Ankrd12
|
APN |
17 |
66,293,169 (GRCm39) |
missense |
probably benign |
|
IGL00555:Ankrd12
|
APN |
17 |
66,291,971 (GRCm39) |
missense |
probably benign |
0.09 |
IGL00790:Ankrd12
|
APN |
17 |
66,291,175 (GRCm39) |
missense |
probably benign |
|
IGL00808:Ankrd12
|
APN |
17 |
66,290,960 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01355:Ankrd12
|
APN |
17 |
66,277,335 (GRCm39) |
splice site |
probably benign |
|
IGL01707:Ankrd12
|
APN |
17 |
66,291,273 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02045:Ankrd12
|
APN |
17 |
66,293,244 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02125:Ankrd12
|
APN |
17 |
66,277,139 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02292:Ankrd12
|
APN |
17 |
66,349,582 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02376:Ankrd12
|
APN |
17 |
66,349,524 (GRCm39) |
intron |
probably benign |
|
IGL02435:Ankrd12
|
APN |
17 |
66,294,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Ankrd12
|
UTSW |
17 |
66,291,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Ankrd12
|
UTSW |
17 |
66,291,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Ankrd12
|
UTSW |
17 |
66,277,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R0195:Ankrd12
|
UTSW |
17 |
66,356,943 (GRCm39) |
splice site |
probably null |
|
R0227:Ankrd12
|
UTSW |
17 |
66,294,222 (GRCm39) |
missense |
probably benign |
0.00 |
R0363:Ankrd12
|
UTSW |
17 |
66,292,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R0366:Ankrd12
|
UTSW |
17 |
66,291,501 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0376:Ankrd12
|
UTSW |
17 |
66,360,004 (GRCm39) |
missense |
probably damaging |
0.98 |
R0470:Ankrd12
|
UTSW |
17 |
66,293,129 (GRCm39) |
missense |
probably benign |
0.00 |
R0480:Ankrd12
|
UTSW |
17 |
66,356,823 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0538:Ankrd12
|
UTSW |
17 |
66,356,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Ankrd12
|
UTSW |
17 |
66,292,127 (GRCm39) |
missense |
probably benign |
0.19 |
R1181:Ankrd12
|
UTSW |
17 |
66,349,569 (GRCm39) |
missense |
probably benign |
0.36 |
R1386:Ankrd12
|
UTSW |
17 |
66,290,375 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1476:Ankrd12
|
UTSW |
17 |
66,293,300 (GRCm39) |
missense |
probably damaging |
0.99 |
R1574:Ankrd12
|
UTSW |
17 |
66,293,269 (GRCm39) |
missense |
probably benign |
0.08 |
R1574:Ankrd12
|
UTSW |
17 |
66,293,269 (GRCm39) |
missense |
probably benign |
0.08 |
R1602:Ankrd12
|
UTSW |
17 |
66,290,683 (GRCm39) |
nonsense |
probably null |
|
R1728:Ankrd12
|
UTSW |
17 |
66,291,071 (GRCm39) |
missense |
probably benign |
0.01 |
R1729:Ankrd12
|
UTSW |
17 |
66,291,071 (GRCm39) |
missense |
probably benign |
0.01 |
R1784:Ankrd12
|
UTSW |
17 |
66,291,071 (GRCm39) |
missense |
probably benign |
0.01 |
R1795:Ankrd12
|
UTSW |
17 |
66,293,222 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1901:Ankrd12
|
UTSW |
17 |
66,293,698 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1929:Ankrd12
|
UTSW |
17 |
66,293,681 (GRCm39) |
missense |
possibly damaging |
0.55 |
R1952:Ankrd12
|
UTSW |
17 |
66,338,566 (GRCm39) |
missense |
probably damaging |
0.98 |
R1997:Ankrd12
|
UTSW |
17 |
66,291,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R2207:Ankrd12
|
UTSW |
17 |
66,338,569 (GRCm39) |
splice site |
probably null |
|
R3612:Ankrd12
|
UTSW |
17 |
66,290,542 (GRCm39) |
missense |
probably benign |
0.01 |
R3768:Ankrd12
|
UTSW |
17 |
66,292,715 (GRCm39) |
missense |
probably benign |
|
R3909:Ankrd12
|
UTSW |
17 |
66,291,000 (GRCm39) |
missense |
probably benign |
0.05 |
R3945:Ankrd12
|
UTSW |
17 |
66,283,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R4176:Ankrd12
|
UTSW |
17 |
66,334,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R4461:Ankrd12
|
UTSW |
17 |
66,292,932 (GRCm39) |
splice site |
probably null |
|
R4628:Ankrd12
|
UTSW |
17 |
66,292,989 (GRCm39) |
missense |
probably benign |
|
R4726:Ankrd12
|
UTSW |
17 |
66,277,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Ankrd12
|
UTSW |
17 |
66,289,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Ankrd12
|
UTSW |
17 |
66,291,632 (GRCm39) |
missense |
probably damaging |
0.99 |
R4847:Ankrd12
|
UTSW |
17 |
66,331,087 (GRCm39) |
missense |
probably benign |
0.14 |
R4858:Ankrd12
|
UTSW |
17 |
66,338,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R5344:Ankrd12
|
UTSW |
17 |
66,356,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R5749:Ankrd12
|
UTSW |
17 |
66,293,091 (GRCm39) |
missense |
probably benign |
0.02 |
R7132:Ankrd12
|
UTSW |
17 |
66,290,242 (GRCm39) |
missense |
probably benign |
|
R7205:Ankrd12
|
UTSW |
17 |
66,292,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R7379:Ankrd12
|
UTSW |
17 |
66,292,242 (GRCm39) |
nonsense |
probably null |
|
R7569:Ankrd12
|
UTSW |
17 |
66,289,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R7570:Ankrd12
|
UTSW |
17 |
66,292,355 (GRCm39) |
missense |
probably benign |
|
R7783:Ankrd12
|
UTSW |
17 |
66,334,245 (GRCm39) |
critical splice donor site |
probably null |
|
R7790:Ankrd12
|
UTSW |
17 |
66,291,225 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7808:Ankrd12
|
UTSW |
17 |
66,292,648 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7834:Ankrd12
|
UTSW |
17 |
66,294,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R7896:Ankrd12
|
UTSW |
17 |
66,292,680 (GRCm39) |
nonsense |
probably null |
|
R7985:Ankrd12
|
UTSW |
17 |
66,291,191 (GRCm39) |
missense |
probably benign |
0.00 |
R8251:Ankrd12
|
UTSW |
17 |
66,291,554 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8304:Ankrd12
|
UTSW |
17 |
66,291,542 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8379:Ankrd12
|
UTSW |
17 |
66,290,939 (GRCm39) |
missense |
probably benign |
0.01 |
R8441:Ankrd12
|
UTSW |
17 |
66,349,546 (GRCm39) |
missense |
probably benign |
0.21 |
R8485:Ankrd12
|
UTSW |
17 |
66,290,711 (GRCm39) |
missense |
probably benign |
0.00 |
R8507:Ankrd12
|
UTSW |
17 |
66,293,904 (GRCm39) |
nonsense |
probably null |
|
R8677:Ankrd12
|
UTSW |
17 |
66,331,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R8790:Ankrd12
|
UTSW |
17 |
66,290,153 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8888:Ankrd12
|
UTSW |
17 |
66,338,568 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8944:Ankrd12
|
UTSW |
17 |
66,277,195 (GRCm39) |
nonsense |
probably null |
|
R8957:Ankrd12
|
UTSW |
17 |
66,291,491 (GRCm39) |
missense |
probably benign |
|
R9069:Ankrd12
|
UTSW |
17 |
66,356,874 (GRCm39) |
missense |
probably benign |
|
R9226:Ankrd12
|
UTSW |
17 |
66,292,754 (GRCm39) |
missense |
probably damaging |
0.99 |
R9275:Ankrd12
|
UTSW |
17 |
66,344,599 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9278:Ankrd12
|
UTSW |
17 |
66,344,599 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9339:Ankrd12
|
UTSW |
17 |
66,291,408 (GRCm39) |
missense |
probably benign |
0.00 |
R9400:Ankrd12
|
UTSW |
17 |
66,291,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R9581:Ankrd12
|
UTSW |
17 |
66,290,415 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Ankrd12
|
UTSW |
17 |
66,277,333 (GRCm39) |
critical splice acceptor site |
probably null |
|
|