Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam29 |
A |
T |
8: 56,324,974 (GRCm39) |
C493* |
probably null |
Het |
Aldh16a1 |
G |
A |
7: 44,795,459 (GRCm39) |
P400L |
probably damaging |
Het |
Anxa5 |
G |
A |
3: 36,506,413 (GRCm39) |
T213I |
probably damaging |
Het |
Baz2b |
A |
G |
2: 59,798,984 (GRCm39) |
L380S |
probably benign |
Het |
Brd8 |
C |
T |
18: 34,735,780 (GRCm39) |
S899N |
probably damaging |
Het |
Cacna2d2 |
C |
T |
9: 107,391,103 (GRCm39) |
Q411* |
probably null |
Het |
Cdh19 |
A |
G |
1: 110,857,614 (GRCm39) |
V240A |
possibly damaging |
Het |
Cltc |
A |
T |
11: 86,595,636 (GRCm39) |
|
probably benign |
Het |
Dclk3 |
T |
A |
9: 111,298,175 (GRCm39) |
V573E |
probably damaging |
Het |
Dhx29 |
T |
C |
13: 113,091,834 (GRCm39) |
|
probably benign |
Het |
Dip2b |
T |
C |
15: 100,084,131 (GRCm39) |
L918P |
possibly damaging |
Het |
Dzip3 |
A |
T |
16: 48,747,959 (GRCm39) |
N1150K |
probably damaging |
Het |
Fgf5 |
T |
C |
5: 98,402,391 (GRCm39) |
S41P |
possibly damaging |
Het |
Galc |
A |
T |
12: 98,197,768 (GRCm39) |
Y120N |
probably damaging |
Het |
Gldc |
T |
C |
19: 30,124,641 (GRCm39) |
N219S |
probably benign |
Het |
Gm11563 |
A |
T |
11: 99,549,631 (GRCm39) |
V41E |
unknown |
Het |
Gpatch11 |
T |
A |
17: 79,147,538 (GRCm39) |
N106K |
probably benign |
Het |
Gpx3 |
A |
G |
11: 54,798,068 (GRCm39) |
N68S |
probably damaging |
Het |
Ibtk |
T |
C |
9: 85,617,123 (GRCm39) |
N150D |
probably damaging |
Het |
Iglc2 |
G |
A |
16: 19,017,462 (GRCm39) |
P48S |
probably benign |
Het |
Itih5 |
G |
A |
2: 10,245,798 (GRCm39) |
R629H |
probably benign |
Het |
Kank1 |
T |
A |
19: 25,388,067 (GRCm39) |
V552E |
possibly damaging |
Het |
Kmt2a |
T |
A |
9: 44,759,983 (GRCm39) |
H655L |
probably damaging |
Het |
Mme |
A |
T |
3: 63,256,070 (GRCm39) |
N510I |
probably damaging |
Het |
Mrtfb |
A |
G |
16: 13,218,047 (GRCm39) |
|
probably null |
Het |
Obscn |
A |
G |
11: 58,913,188 (GRCm39) |
I6943T |
probably damaging |
Het |
Obscn |
G |
T |
11: 58,984,152 (GRCm39) |
Q1768K |
possibly damaging |
Het |
Or51k2 |
T |
A |
7: 103,596,279 (GRCm39) |
C169S |
probably damaging |
Het |
Or5ac25 |
T |
C |
16: 59,181,879 (GRCm39) |
N234S |
probably benign |
Het |
Otud3 |
A |
T |
4: 138,624,025 (GRCm39) |
|
probably null |
Het |
Parp4 |
A |
G |
14: 56,827,959 (GRCm39) |
K237E |
probably benign |
Het |
Pfkfb4 |
C |
T |
9: 108,854,178 (GRCm39) |
R351W |
probably damaging |
Het |
Pttg1ip2 |
T |
C |
5: 5,500,644 (GRCm39) |
*151W |
probably null |
Het |
Rbbp6 |
T |
C |
7: 122,570,352 (GRCm39) |
|
probably null |
Het |
Rdh16 |
G |
T |
10: 127,647,188 (GRCm39) |
|
probably benign |
Het |
Ropn1 |
A |
G |
16: 34,487,147 (GRCm39) |
T28A |
probably benign |
Het |
Sec24d |
T |
C |
3: 123,152,607 (GRCm39) |
V873A |
probably damaging |
Het |
Serpinb3b |
T |
A |
1: 107,082,474 (GRCm39) |
L263F |
probably damaging |
Het |
Shq1 |
T |
C |
6: 100,607,967 (GRCm39) |
T315A |
probably benign |
Het |
Slc13a4 |
T |
C |
6: 35,255,223 (GRCm39) |
E355G |
probably benign |
Het |
Slc26a9 |
T |
C |
1: 131,687,175 (GRCm39) |
S445P |
probably damaging |
Het |
Slc39a10 |
G |
A |
1: 46,857,288 (GRCm39) |
A696V |
probably damaging |
Het |
Slc4a10 |
A |
T |
2: 62,098,515 (GRCm39) |
M550L |
probably benign |
Het |
Spata31e5 |
T |
C |
1: 28,815,419 (GRCm39) |
N871S |
possibly damaging |
Het |
Syt17 |
T |
C |
7: 118,009,197 (GRCm39) |
D341G |
probably benign |
Het |
Tmem62 |
A |
G |
2: 120,826,993 (GRCm39) |
Y430C |
probably benign |
Het |
Upp1 |
A |
G |
11: 9,075,650 (GRCm39) |
|
probably benign |
Het |
Vmn1r91 |
T |
G |
7: 19,835,429 (GRCm39) |
V116G |
probably damaging |
Het |
Vmn2r101 |
A |
T |
17: 19,809,963 (GRCm39) |
I250F |
possibly damaging |
Het |
Vmn2r116 |
T |
G |
17: 23,616,601 (GRCm39) |
|
probably benign |
Het |
Vmn2r72 |
C |
T |
7: 85,399,919 (GRCm39) |
V377I |
probably benign |
Het |
Zfp592 |
G |
T |
7: 80,687,932 (GRCm39) |
A953S |
probably benign |
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 |
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 |
IGL02530:Ankrd12
|
APN |
17 |
66,291,398 (GRCm39) |
missense |
probably benign |
0.20 |
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 |
|
|