Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
A |
G |
11: 109,867,299 (GRCm39) |
L253S |
probably damaging |
Het |
Adgrv1 |
T |
C |
13: 81,726,261 (GRCm39) |
E588G |
probably benign |
Het |
Ahcy |
G |
A |
2: 154,910,893 (GRCm39) |
A25V |
probably damaging |
Het |
Ank2 |
A |
C |
3: 126,797,631 (GRCm39) |
L710R |
probably damaging |
Het |
Ap1b1 |
A |
G |
11: 4,989,558 (GRCm39) |
T824A |
probably benign |
Het |
Arap2 |
T |
A |
5: 62,763,551 (GRCm39) |
H1531L |
probably damaging |
Het |
Atosb |
A |
T |
4: 43,036,434 (GRCm39) |
V99E |
probably benign |
Het |
B3gnt7 |
T |
C |
1: 86,233,495 (GRCm39) |
L247P |
probably damaging |
Het |
Bcl6b |
A |
G |
11: 70,117,396 (GRCm39) |
C409R |
probably damaging |
Het |
Bicdl1 |
T |
C |
5: 115,808,229 (GRCm39) |
H301R |
probably benign |
Het |
Casc3 |
T |
A |
11: 98,718,413 (GRCm39) |
I491N |
possibly damaging |
Het |
Ccdc92b |
T |
A |
11: 74,520,887 (GRCm39) |
L63Q |
probably damaging |
Het |
Cep250 |
A |
G |
2: 155,837,314 (GRCm39) |
T2319A |
probably benign |
Het |
Chd1 |
T |
C |
17: 15,981,628 (GRCm39) |
S1356P |
probably damaging |
Het |
Chd8 |
A |
G |
14: 52,450,129 (GRCm39) |
S1542P |
probably benign |
Het |
Clec2m |
A |
G |
6: 129,299,915 (GRCm39) |
C188R |
probably damaging |
Het |
Cntnap4 |
A |
G |
8: 113,542,120 (GRCm39) |
D751G |
probably damaging |
Het |
Cpsf4l |
G |
A |
11: 113,593,315 (GRCm39) |
R90C |
possibly damaging |
Het |
Defa21 |
G |
A |
8: 21,515,724 (GRCm39) |
A41T |
probably damaging |
Het |
Dennd4a |
G |
T |
9: 64,801,681 (GRCm39) |
L941F |
possibly damaging |
Het |
Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
Dtx4 |
A |
T |
19: 12,450,624 (GRCm39) |
C529* |
probably null |
Het |
Entpd3 |
A |
G |
9: 120,389,665 (GRCm39) |
Y317C |
probably damaging |
Het |
Erp29 |
T |
A |
5: 121,583,381 (GRCm39) |
I182F |
possibly damaging |
Het |
Fam161a |
A |
G |
11: 22,973,452 (GRCm39) |
R445G |
possibly damaging |
Het |
Fam76a |
T |
A |
4: 132,631,232 (GRCm39) |
M238L |
possibly damaging |
Het |
Fn1 |
T |
C |
1: 71,666,408 (GRCm39) |
Y875C |
probably damaging |
Het |
Gnb2 |
A |
G |
5: 137,528,444 (GRCm39) |
|
probably null |
Het |
Hspg2 |
T |
C |
4: 137,237,963 (GRCm39) |
S229P |
probably damaging |
Het |
Ighv6-6 |
A |
G |
12: 114,398,590 (GRCm39) |
S59P |
probably damaging |
Het |
Itpkc |
C |
A |
7: 26,927,702 (GRCm39) |
A71S |
probably benign |
Het |
Kcnk10 |
G |
A |
12: 98,485,002 (GRCm39) |
R45* |
probably null |
Het |
Krcc1 |
A |
G |
6: 71,261,198 (GRCm39) |
S77G |
probably benign |
Het |
Lelp1 |
G |
A |
3: 92,042,821 (GRCm39) |
T76I |
unknown |
Het |
Lifr |
A |
T |
15: 7,208,421 (GRCm39) |
I600F |
possibly damaging |
Het |
Lrrk1 |
T |
A |
7: 65,937,191 (GRCm39) |
D987V |
possibly damaging |
Het |
Muc16 |
C |
T |
9: 18,548,594 (GRCm39) |
D5900N |
probably benign |
Het |
Muc6 |
AGGCGCAGAAACCCTGGC |
AGGC |
7: 141,214,363 (GRCm39) |
|
probably null |
Het |
Myo9a |
A |
G |
9: 59,778,098 (GRCm39) |
I1285V |
probably benign |
Het |
Ndel1 |
T |
C |
11: 68,713,474 (GRCm39) |
D321G |
possibly damaging |
Het |
Nlrp4b |
T |
C |
7: 10,449,144 (GRCm39) |
V449A |
probably damaging |
Het |
Or10q12 |
A |
G |
19: 13,746,525 (GRCm39) |
E273G |
probably benign |
Het |
Or2r11 |
T |
C |
6: 42,437,488 (GRCm39) |
N155S |
possibly damaging |
Het |
Or2y1c |
T |
A |
11: 49,361,261 (GRCm39) |
Y94* |
probably null |
Het |
Or51k1 |
A |
T |
7: 103,661,489 (GRCm39) |
L140Q |
probably benign |
Het |
Or5k3 |
A |
C |
16: 58,969,279 (GRCm39) |
D22A |
probably benign |
Het |
Osbpl1a |
G |
A |
18: 12,974,310 (GRCm39) |
R459* |
probably null |
Het |
Pabpc1l |
A |
C |
2: 163,884,399 (GRCm39) |
T379P |
probably damaging |
Het |
Pde2a |
A |
T |
7: 101,071,175 (GRCm39) |
Q15L |
probably benign |
Het |
Pdk1 |
A |
G |
2: 71,726,085 (GRCm39) |
N331S |
probably benign |
Het |
Pfdn1 |
A |
T |
18: 36,584,519 (GRCm39) |
|
probably null |
Het |
Pnliprp1 |
T |
A |
19: 58,717,582 (GRCm39) |
L9H |
probably damaging |
Het |
Prl7a2 |
A |
T |
13: 27,843,076 (GRCm39) |
D242E |
possibly damaging |
Het |
Prmt9 |
T |
A |
8: 78,294,880 (GRCm39) |
I408N |
possibly damaging |
Het |
Psme4 |
G |
A |
11: 30,798,105 (GRCm39) |
R1366H |
probably benign |
Het |
Pstpip1 |
A |
T |
9: 56,035,934 (GRCm39) |
D393V |
probably damaging |
Het |
Rab5b |
A |
G |
10: 128,519,062 (GRCm39) |
|
probably null |
Het |
Rap1gap2 |
G |
A |
11: 74,283,945 (GRCm39) |
R618C |
probably damaging |
Het |
Rin1 |
A |
G |
19: 5,100,801 (GRCm39) |
|
probably benign |
Het |
Sall3 |
G |
A |
18: 81,016,969 (GRCm39) |
P320S |
probably benign |
Het |
Sdk1 |
A |
G |
5: 142,067,471 (GRCm39) |
T1124A |
probably damaging |
Het |
Sirpb1c |
T |
A |
3: 15,892,941 (GRCm39) |
T88S |
possibly damaging |
Het |
Slc35f6 |
T |
A |
5: 30,814,121 (GRCm39) |
I189N |
probably damaging |
Het |
Slc49a3 |
T |
A |
5: 108,596,581 (GRCm39) |
|
probably null |
Het |
Spata31d1e |
T |
A |
13: 59,889,997 (GRCm39) |
R608* |
probably null |
Het |
Spsb2 |
A |
T |
6: 124,787,244 (GRCm39) |
Q226L |
probably benign |
Het |
Stab2 |
T |
C |
10: 86,741,456 (GRCm39) |
D1221G |
possibly damaging |
Het |
Sugp1 |
G |
A |
8: 70,522,800 (GRCm39) |
R500H |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,082,078 (GRCm39) |
Y849H |
probably damaging |
Het |
Tbck |
T |
A |
3: 132,428,092 (GRCm39) |
I249N |
possibly damaging |
Het |
Tdrd6 |
A |
C |
17: 43,935,095 (GRCm39) |
F1984L |
probably benign |
Het |
Tnxb |
T |
A |
17: 34,890,314 (GRCm39) |
V219E |
unknown |
Het |
Tpst1 |
T |
A |
5: 130,143,344 (GRCm39) |
V294D |
probably damaging |
Het |
Treml1 |
A |
G |
17: 48,667,247 (GRCm39) |
Q44R |
probably damaging |
Het |
Trrap |
G |
A |
5: 144,733,945 (GRCm39) |
A933T |
probably benign |
Het |
Vars2 |
A |
G |
17: 35,969,142 (GRCm39) |
L853P |
probably damaging |
Het |
Vmn1r10 |
A |
T |
6: 57,090,615 (GRCm39) |
N69I |
possibly damaging |
Het |
Vmn1r179 |
T |
A |
7: 23,627,819 (GRCm39) |
Y3* |
probably null |
Het |
Vmn2r38 |
T |
A |
7: 9,093,728 (GRCm39) |
Y498F |
probably benign |
Het |
Zc3h11a |
T |
C |
1: 133,566,655 (GRCm39) |
T179A |
probably damaging |
Het |
|
Other mutations in Zmym2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00516:Zmym2
|
APN |
14 |
57,185,394 (GRCm39) |
splice site |
probably benign |
|
IGL00587:Zmym2
|
APN |
14 |
57,140,817 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL00736:Zmym2
|
APN |
14 |
57,140,668 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00753:Zmym2
|
APN |
14 |
57,194,517 (GRCm39) |
nonsense |
probably null |
|
IGL01608:Zmym2
|
APN |
14 |
57,185,472 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL01744:Zmym2
|
APN |
14 |
57,184,029 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02150:Zmym2
|
APN |
14 |
57,148,526 (GRCm39) |
splice site |
probably benign |
|
IGL02186:Zmym2
|
APN |
14 |
57,180,808 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02654:Zmym2
|
APN |
14 |
57,148,772 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02960:Zmym2
|
APN |
14 |
57,175,870 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03104:Zmym2
|
APN |
14 |
57,187,784 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03162:Zmym2
|
APN |
14 |
57,151,500 (GRCm39) |
missense |
probably benign |
0.24 |
IGL03356:Zmym2
|
APN |
14 |
57,194,517 (GRCm39) |
nonsense |
probably null |
|
IGL03412:Zmym2
|
APN |
14 |
57,197,176 (GRCm39) |
nonsense |
probably null |
|
R5038_Zmym2_756
|
UTSW |
14 |
57,193,637 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0131:Zmym2
|
UTSW |
14 |
57,180,715 (GRCm39) |
missense |
probably benign |
|
R0131:Zmym2
|
UTSW |
14 |
57,180,715 (GRCm39) |
missense |
probably benign |
|
R0132:Zmym2
|
UTSW |
14 |
57,180,715 (GRCm39) |
missense |
probably benign |
|
R0270:Zmym2
|
UTSW |
14 |
57,187,141 (GRCm39) |
splice site |
probably null |
|
R0834:Zmym2
|
UTSW |
14 |
57,194,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R1071:Zmym2
|
UTSW |
14 |
57,197,278 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1386:Zmym2
|
UTSW |
14 |
57,150,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Zmym2
|
UTSW |
14 |
57,180,784 (GRCm39) |
missense |
probably damaging |
0.99 |
R1472:Zmym2
|
UTSW |
14 |
57,148,640 (GRCm39) |
missense |
probably benign |
0.20 |
R1595:Zmym2
|
UTSW |
14 |
57,158,187 (GRCm39) |
missense |
probably benign |
0.25 |
R1598:Zmym2
|
UTSW |
14 |
57,151,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R1598:Zmym2
|
UTSW |
14 |
57,140,226 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1916:Zmym2
|
UTSW |
14 |
57,197,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R2261:Zmym2
|
UTSW |
14 |
57,165,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R2393:Zmym2
|
UTSW |
14 |
57,158,180 (GRCm39) |
missense |
probably benign |
0.17 |
R2866:Zmym2
|
UTSW |
14 |
57,165,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R3727:Zmym2
|
UTSW |
14 |
57,156,806 (GRCm39) |
splice site |
probably benign |
|
R3847:Zmym2
|
UTSW |
14 |
57,158,956 (GRCm39) |
splice site |
probably benign |
|
R4043:Zmym2
|
UTSW |
14 |
57,195,765 (GRCm39) |
splice site |
probably benign |
|
R4074:Zmym2
|
UTSW |
14 |
57,140,461 (GRCm39) |
missense |
probably damaging |
0.99 |
R4343:Zmym2
|
UTSW |
14 |
57,159,019 (GRCm39) |
missense |
probably damaging |
0.99 |
R4420:Zmym2
|
UTSW |
14 |
57,194,335 (GRCm39) |
missense |
probably damaging |
0.98 |
R4645:Zmym2
|
UTSW |
14 |
57,165,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Zmym2
|
UTSW |
14 |
57,159,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R5038:Zmym2
|
UTSW |
14 |
57,193,637 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5223:Zmym2
|
UTSW |
14 |
57,183,971 (GRCm39) |
missense |
probably benign |
|
R5364:Zmym2
|
UTSW |
14 |
57,158,102 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5488:Zmym2
|
UTSW |
14 |
57,193,712 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5489:Zmym2
|
UTSW |
14 |
57,193,712 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5818:Zmym2
|
UTSW |
14 |
57,183,986 (GRCm39) |
missense |
probably benign |
|
R6160:Zmym2
|
UTSW |
14 |
57,187,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R6437:Zmym2
|
UTSW |
14 |
57,140,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R7153:Zmym2
|
UTSW |
14 |
57,187,659 (GRCm39) |
missense |
probably benign |
0.16 |
R7337:Zmym2
|
UTSW |
14 |
57,181,557 (GRCm39) |
missense |
probably benign |
0.04 |
R7535:Zmym2
|
UTSW |
14 |
57,194,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R7730:Zmym2
|
UTSW |
14 |
57,193,638 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7779:Zmym2
|
UTSW |
14 |
57,165,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R7849:Zmym2
|
UTSW |
14 |
57,184,020 (GRCm39) |
missense |
probably benign |
0.03 |
R8219:Zmym2
|
UTSW |
14 |
57,163,316 (GRCm39) |
missense |
probably benign |
0.07 |
R8493:Zmym2
|
UTSW |
14 |
57,151,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R8885:Zmym2
|
UTSW |
14 |
57,185,329 (GRCm39) |
intron |
probably benign |
|
R9162:Zmym2
|
UTSW |
14 |
57,163,361 (GRCm39) |
missense |
probably benign |
0.02 |
R9165:Zmym2
|
UTSW |
14 |
57,185,464 (GRCm39) |
missense |
probably damaging |
0.98 |
R9250:Zmym2
|
UTSW |
14 |
57,148,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R9453:Zmym2
|
UTSW |
14 |
57,180,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R9677:Zmym2
|
UTSW |
14 |
57,187,115 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Zmym2
|
UTSW |
14 |
57,150,456 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1177:Zmym2
|
UTSW |
14 |
57,151,419 (GRCm39) |
missense |
probably damaging |
1.00 |
|