Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
A |
T |
11: 109,871,708 (GRCm39) |
M90K |
probably damaging |
Het |
Actn2 |
T |
C |
13: 12,303,516 (GRCm39) |
D428G |
probably damaging |
Het |
Arrb1 |
T |
C |
7: 99,243,836 (GRCm39) |
V262A |
probably damaging |
Het |
Bok |
A |
G |
1: 93,622,661 (GRCm39) |
I102V |
|
Het |
C87436 |
T |
A |
6: 86,439,567 (GRCm39) |
F419L |
probably damaging |
Het |
Capn15 |
A |
G |
17: 26,192,141 (GRCm39) |
C34R |
probably benign |
Het |
Ccdc8 |
T |
A |
7: 16,728,800 (GRCm39) |
Y96* |
probably null |
Het |
Cd274 |
T |
A |
19: 29,357,771 (GRCm39) |
C154* |
probably null |
Het |
Cfap251 |
A |
G |
5: 123,418,082 (GRCm39) |
|
probably benign |
Het |
Ckap4 |
A |
T |
10: 84,369,402 (GRCm39) |
L110Q |
probably damaging |
Het |
Col26a1 |
A |
T |
5: 136,777,202 (GRCm39) |
D335E |
probably benign |
Het |
Crybg1 |
C |
T |
10: 43,874,844 (GRCm39) |
V755I |
probably benign |
Het |
Dhx38 |
A |
T |
8: 110,282,783 (GRCm39) |
Y628N |
probably damaging |
Het |
Dnah12 |
A |
T |
14: 26,492,325 (GRCm39) |
K1155M |
probably benign |
Het |
Ei24 |
A |
G |
9: 36,697,270 (GRCm39) |
F153L |
probably damaging |
Het |
Erg |
T |
A |
16: 95,178,188 (GRCm39) |
E246D |
probably benign |
Het |
Exoc6b |
T |
C |
6: 84,982,000 (GRCm39) |
N99D |
possibly damaging |
Het |
Fam222b |
G |
T |
11: 78,046,020 (GRCm39) |
R527L |
probably damaging |
Het |
Fam83h |
T |
C |
15: 75,875,135 (GRCm39) |
Y734C |
probably damaging |
Het |
Fbxo43 |
T |
C |
15: 36,162,619 (GRCm39) |
E196G |
possibly damaging |
Het |
Gata5 |
G |
A |
2: 179,976,131 (GRCm39) |
P11L |
possibly damaging |
Het |
Gbp3 |
A |
T |
3: 142,271,048 (GRCm39) |
S151C |
probably benign |
Het |
Gli3 |
T |
C |
13: 15,901,320 (GRCm39) |
L1569P |
probably damaging |
Het |
Helz |
G |
A |
11: 107,523,041 (GRCm39) |
V742M |
probably damaging |
Het |
Ifi27l2b |
A |
T |
12: 103,418,114 (GRCm39) |
N175K |
unknown |
Het |
Itga1 |
A |
T |
13: 115,185,856 (GRCm39) |
Y49N |
probably damaging |
Het |
Kcnk2 |
T |
C |
1: 188,991,072 (GRCm39) |
T167A |
probably damaging |
Het |
Kirrel2 |
T |
A |
7: 30,147,642 (GRCm39) |
T669S |
probably benign |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Lrit2 |
A |
T |
14: 36,790,812 (GRCm39) |
T164S |
possibly damaging |
Het |
Lrriq1 |
A |
G |
10: 103,051,864 (GRCm39) |
V296A |
probably damaging |
Het |
Malsu1 |
C |
T |
6: 49,050,731 (GRCm39) |
|
probably benign |
Het |
Nfs1 |
C |
T |
2: 155,968,934 (GRCm39) |
G380E |
probably damaging |
Het |
Nol4l |
C |
A |
2: 153,312,630 (GRCm39) |
R226L |
probably damaging |
Het |
Nsmaf |
CAAACTTTTAAACTT |
CAAACTT |
4: 6,416,543 (GRCm39) |
|
probably null |
Het |
Nup98 |
T |
A |
7: 101,844,173 (GRCm39) |
N54I |
probably damaging |
Het |
Or7g21 |
C |
T |
9: 19,032,890 (GRCm39) |
P210L |
probably benign |
Het |
Or8g22 |
A |
T |
9: 38,958,026 (GRCm39) |
C230S |
probably benign |
Het |
Or8g53 |
A |
G |
9: 39,683,514 (GRCm39) |
I194T |
|
Het |
Otoa |
T |
A |
7: 120,739,055 (GRCm39) |
F755I |
probably benign |
Het |
P4htm |
A |
T |
9: 108,460,911 (GRCm39) |
M187K |
probably benign |
Het |
Phldb3 |
C |
T |
7: 24,323,727 (GRCm39) |
R453C |
probably benign |
Het |
Pkd1l1 |
C |
T |
11: 8,922,986 (GRCm39) |
A94T |
|
Het |
Pkp1 |
A |
G |
1: 135,805,429 (GRCm39) |
F669S |
probably benign |
Het |
Prl8a2 |
C |
G |
13: 27,536,793 (GRCm39) |
Y138* |
probably null |
Het |
Prl8a2 |
T |
A |
13: 27,536,794 (GRCm39) |
Y139N |
probably benign |
Het |
Rtn4r |
T |
A |
16: 17,969,068 (GRCm39) |
N165K |
probably benign |
Het |
Scaper |
G |
T |
9: 55,669,616 (GRCm39) |
D353E |
probably damaging |
Het |
Scn4a |
G |
T |
11: 106,211,000 (GRCm39) |
D1672E |
probably damaging |
Het |
She |
A |
G |
3: 89,739,078 (GRCm39) |
S90G |
probably benign |
Het |
Shmt2 |
A |
T |
10: 127,355,962 (GRCm39) |
D130E |
possibly damaging |
Het |
Slc2a12 |
T |
A |
10: 22,569,923 (GRCm39) |
I538K |
possibly damaging |
Het |
Snx29 |
T |
A |
16: 11,478,435 (GRCm39) |
W322R |
probably damaging |
Het |
Spp1 |
A |
G |
5: 104,588,387 (GRCm39) |
D263G |
probably benign |
Het |
Srek1ip1 |
T |
C |
13: 104,973,964 (GRCm39) |
S124P |
possibly damaging |
Het |
Tcp10b |
C |
T |
17: 13,280,656 (GRCm39) |
|
probably benign |
Het |
Thap12 |
T |
C |
7: 98,364,600 (GRCm39) |
F256S |
probably damaging |
Het |
Tpte |
T |
C |
8: 22,845,497 (GRCm39) |
Y516H |
|
Het |
Trem1 |
C |
A |
17: 48,544,271 (GRCm39) |
Q99K |
possibly damaging |
Het |
Umodl1 |
C |
T |
17: 31,178,147 (GRCm39) |
P41L |
probably benign |
Het |
Upp2 |
T |
C |
2: 58,457,542 (GRCm39) |
|
probably null |
Het |
Zfand1 |
A |
T |
3: 10,406,148 (GRCm39) |
M181K |
probably damaging |
Het |
Zfp292 |
T |
C |
4: 34,809,228 (GRCm39) |
E1277G |
possibly damaging |
Het |
Zfp458 |
G |
T |
13: 67,405,696 (GRCm39) |
P248T |
probably damaging |
Het |
Zfp667 |
T |
A |
7: 6,308,322 (GRCm39) |
M330K |
probably benign |
Het |
Zfp827 |
A |
G |
8: 79,917,107 (GRCm39) |
T561A |
|
Het |
Zfp947 |
C |
T |
17: 22,364,855 (GRCm39) |
G273D |
probably benign |
Het |
|
Other mutations in Moxd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Moxd1
|
APN |
10 |
24,155,762 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00227:Moxd1
|
APN |
10 |
24,158,491 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00331:Moxd1
|
APN |
10 |
24,158,453 (GRCm39) |
splice site |
probably benign |
|
IGL01074:Moxd1
|
APN |
10 |
24,155,282 (GRCm39) |
missense |
probably benign |
0.45 |
IGL01462:Moxd1
|
APN |
10 |
24,120,286 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01777:Moxd1
|
APN |
10 |
24,128,494 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02051:Moxd1
|
APN |
10 |
24,128,916 (GRCm39) |
splice site |
probably null |
|
IGL02272:Moxd1
|
APN |
10 |
24,158,598 (GRCm39) |
nonsense |
probably null |
|
IGL02343:Moxd1
|
APN |
10 |
24,155,762 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02425:Moxd1
|
APN |
10 |
24,155,334 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02448:Moxd1
|
APN |
10 |
24,158,617 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02452:Moxd1
|
APN |
10 |
24,158,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03301:Moxd1
|
APN |
10 |
24,155,382 (GRCm39) |
missense |
probably damaging |
0.99 |
R0631:Moxd1
|
UTSW |
10 |
24,128,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R1436:Moxd1
|
UTSW |
10 |
24,120,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Moxd1
|
UTSW |
10 |
24,099,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Moxd1
|
UTSW |
10 |
24,176,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Moxd1
|
UTSW |
10 |
24,176,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Moxd1
|
UTSW |
10 |
24,157,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Moxd1
|
UTSW |
10 |
24,155,781 (GRCm39) |
missense |
probably benign |
0.17 |
R3115:Moxd1
|
UTSW |
10 |
24,177,429 (GRCm39) |
nonsense |
probably null |
|
R3116:Moxd1
|
UTSW |
10 |
24,177,429 (GRCm39) |
nonsense |
probably null |
|
R5183:Moxd1
|
UTSW |
10 |
24,155,445 (GRCm39) |
critical splice donor site |
probably null |
|
R5183:Moxd1
|
UTSW |
10 |
24,163,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R5322:Moxd1
|
UTSW |
10 |
24,120,151 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5728:Moxd1
|
UTSW |
10 |
24,099,581 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5824:Moxd1
|
UTSW |
10 |
24,162,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Moxd1
|
UTSW |
10 |
24,160,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R6322:Moxd1
|
UTSW |
10 |
24,160,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R6662:Moxd1
|
UTSW |
10 |
24,160,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R6827:Moxd1
|
UTSW |
10 |
24,155,748 (GRCm39) |
missense |
probably benign |
0.29 |
R6928:Moxd1
|
UTSW |
10 |
24,176,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7048:Moxd1
|
UTSW |
10 |
24,157,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Moxd1
|
UTSW |
10 |
24,177,363 (GRCm39) |
missense |
probably benign |
0.05 |
R7736:Moxd1
|
UTSW |
10 |
24,158,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R8060:Moxd1
|
UTSW |
10 |
24,177,510 (GRCm39) |
missense |
unknown |
|
R8073:Moxd1
|
UTSW |
10 |
24,128,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R8089:Moxd1
|
UTSW |
10 |
24,157,417 (GRCm39) |
missense |
probably benign |
0.43 |
R8255:Moxd1
|
UTSW |
10 |
24,099,700 (GRCm39) |
missense |
probably benign |
0.02 |
R8314:Moxd1
|
UTSW |
10 |
24,128,438 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9039:Moxd1
|
UTSW |
10 |
24,155,251 (GRCm39) |
splice site |
probably benign |
|
R9306:Moxd1
|
UTSW |
10 |
24,128,824 (GRCm39) |
splice site |
probably benign |
|
R9657:Moxd1
|
UTSW |
10 |
24,128,485 (GRCm39) |
missense |
probably benign |
0.16 |
X0063:Moxd1
|
UTSW |
10 |
24,128,398 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Moxd1
|
UTSW |
10 |
24,160,702 (GRCm39) |
missense |
probably benign |
|
|