Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
T |
A |
8: 111,767,361 (GRCm39) |
W156R |
probably damaging |
Het |
Acvr1 |
T |
A |
2: 58,364,286 (GRCm39) |
|
probably null |
Het |
Adamts2 |
G |
T |
11: 50,494,315 (GRCm39) |
V130L |
probably damaging |
Het |
Adcy4 |
C |
T |
14: 56,012,697 (GRCm39) |
V541I |
probably benign |
Het |
Adgrl2 |
C |
T |
3: 148,552,542 (GRCm39) |
V654I |
probably damaging |
Het |
Ago3 |
T |
A |
4: 126,270,721 (GRCm39) |
K258* |
probably null |
Het |
Akap11 |
A |
T |
14: 78,749,929 (GRCm39) |
S819R |
|
Het |
Alox5ap |
T |
C |
5: 149,224,419 (GRCm39) |
F121L |
probably damaging |
Het |
Baz2b |
A |
T |
2: 59,731,858 (GRCm39) |
M2060K |
probably damaging |
Het |
Bltp3b |
T |
C |
10: 89,627,281 (GRCm39) |
S449P |
probably benign |
Het |
C030005K15Rik |
T |
C |
10: 97,561,414 (GRCm39) |
I106V |
unknown |
Het |
Ccdc121rt2 |
C |
T |
5: 112,598,653 (GRCm39) |
T400I |
probably benign |
Het |
Cdhr1 |
T |
C |
14: 36,813,935 (GRCm39) |
T164A |
probably benign |
Het |
Dhx30 |
T |
C |
9: 109,914,569 (GRCm39) |
E976G |
possibly damaging |
Het |
Dnah17 |
C |
T |
11: 118,005,021 (GRCm39) |
G788R |
probably benign |
Het |
Dus2 |
T |
C |
8: 106,722,645 (GRCm39) |
|
probably benign |
Het |
Etv6 |
T |
C |
6: 134,225,717 (GRCm39) |
V316A |
possibly damaging |
Het |
Fabp9 |
T |
G |
3: 10,259,085 (GRCm39) |
K107T |
possibly damaging |
Het |
Fmn2 |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
1: 174,436,769 (GRCm39) |
|
probably benign |
Het |
Gapdh |
A |
G |
6: 125,140,226 (GRCm39) |
V92A |
probably benign |
Het |
Gfy |
A |
G |
7: 44,826,019 (GRCm39) |
L453P |
probably damaging |
Het |
Gp2 |
C |
T |
7: 119,042,010 (GRCm39) |
C505Y |
probably benign |
Het |
Gtpbp8 |
T |
C |
16: 44,566,676 (GRCm39) |
R9G |
probably benign |
Het |
Hipk4 |
G |
T |
7: 27,223,033 (GRCm39) |
R31L |
probably damaging |
Het |
Htt |
T |
A |
5: 35,063,068 (GRCm39) |
M2900K |
probably damaging |
Het |
Ighv1-20 |
T |
C |
12: 114,687,810 (GRCm39) |
I6V |
probably benign |
Het |
Il17d |
C |
T |
14: 57,779,937 (GRCm39) |
T153I |
probably damaging |
Het |
Izumo3 |
T |
A |
4: 92,034,581 (GRCm39) |
N117I |
probably damaging |
Het |
Kcnh7 |
T |
C |
2: 62,680,879 (GRCm39) |
D236G |
probably benign |
Het |
Kmt2d |
T |
C |
15: 98,750,478 (GRCm39) |
D2405G |
unknown |
Het |
Map4k2 |
T |
C |
19: 6,396,596 (GRCm39) |
W533R |
probably damaging |
Het |
Matn1 |
C |
A |
4: 130,673,300 (GRCm39) |
Y89* |
probably null |
Het |
Mettl18 |
T |
A |
1: 163,824,509 (GRCm39) |
Y277N |
probably damaging |
Het |
Muc5b |
G |
A |
7: 141,417,898 (GRCm39) |
G3615S |
probably benign |
Het |
Mycbp2 |
A |
C |
14: 103,398,111 (GRCm39) |
|
probably null |
Het |
Myh4 |
T |
A |
11: 67,143,390 (GRCm39) |
S1041T |
possibly damaging |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Naaladl1 |
T |
C |
19: 6,159,703 (GRCm39) |
V378A |
possibly damaging |
Het |
Nars1 |
T |
C |
18: 64,637,458 (GRCm39) |
D374G |
probably benign |
Het |
Neb |
C |
T |
2: 52,198,283 (GRCm39) |
|
probably null |
Het |
Neurl1b |
A |
G |
17: 26,650,965 (GRCm39) |
Y79C |
probably damaging |
Het |
Nynrin |
A |
G |
14: 56,101,248 (GRCm39) |
T306A |
probably benign |
Het |
Ola1 |
G |
T |
2: 73,029,745 (GRCm39) |
R125S |
probably damaging |
Het |
Or12d15 |
T |
A |
17: 37,694,122 (GRCm39) |
F221L |
probably benign |
Het |
Or51a43 |
A |
T |
7: 103,717,383 (GRCm39) |
V285D |
probably damaging |
Het |
Pak1ip1 |
C |
A |
13: 41,158,214 (GRCm39) |
T29K |
probably benign |
Het |
Podnl1 |
T |
A |
8: 84,857,402 (GRCm39) |
L337H |
|
Het |
Rictor |
T |
G |
15: 6,807,800 (GRCm39) |
|
probably null |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Sel1l2 |
T |
C |
2: 140,072,753 (GRCm39) |
I627M |
probably benign |
Het |
Sh3rf2 |
T |
C |
18: 42,244,493 (GRCm39) |
S352P |
probably damaging |
Het |
Slc6a6 |
G |
A |
6: 91,703,224 (GRCm39) |
W199* |
probably null |
Het |
Smc2 |
T |
A |
4: 52,450,965 (GRCm39) |
V261E |
probably benign |
Het |
Sorcs3 |
G |
A |
19: 48,692,808 (GRCm39) |
|
probably null |
Het |
Spdye4a |
T |
A |
5: 143,211,562 (GRCm39) |
M1L |
probably benign |
Het |
Stag1 |
T |
C |
9: 100,639,819 (GRCm39) |
I125T |
possibly damaging |
Het |
Stx8 |
T |
A |
11: 67,911,814 (GRCm39) |
D177E |
probably benign |
Het |
Sun2 |
T |
C |
15: 79,623,125 (GRCm39) |
Y71C |
probably damaging |
Het |
Tmed9 |
T |
C |
13: 55,742,617 (GRCm39) |
F129L |
probably benign |
Het |
Tmem216 |
T |
A |
19: 10,529,336 (GRCm39) |
T17S |
probably benign |
Het |
Tmpo |
A |
T |
10: 90,997,974 (GRCm39) |
N604K |
probably benign |
Het |
Tmprss11f |
T |
A |
5: 86,681,666 (GRCm39) |
I196F |
probably benign |
Het |
Tnks |
A |
G |
8: 35,301,738 (GRCm39) |
F1244L |
probably benign |
Het |
Tspan2 |
T |
C |
3: 102,676,226 (GRCm39) |
C212R |
probably damaging |
Het |
Tspan4 |
A |
G |
7: 141,071,718 (GRCm39) |
D155G |
probably damaging |
Het |
Ttc6 |
T |
C |
12: 57,707,282 (GRCm39) |
F730L |
possibly damaging |
Het |
Txnrd2 |
G |
A |
16: 18,245,291 (GRCm39) |
A33T |
unknown |
Het |
Wnk1 |
C |
T |
6: 119,940,454 (GRCm39) |
R761H |
probably damaging |
Het |
Zfp217 |
T |
C |
2: 169,962,024 (GRCm39) |
D101G |
probably damaging |
Het |
Zfp281 |
T |
C |
1: 136,555,620 (GRCm39) |
F866S |
probably damaging |
Het |
|
Other mutations in Carmil2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Carmil2
|
APN |
8 |
106,418,038 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01295:Carmil2
|
APN |
8 |
106,422,148 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02055:Carmil2
|
APN |
8 |
106,423,539 (GRCm39) |
splice site |
probably benign |
|
IGL02532:Carmil2
|
APN |
8 |
106,419,063 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02900:Carmil2
|
APN |
8 |
106,422,151 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03242:Carmil2
|
APN |
8 |
106,417,952 (GRCm39) |
splice site |
probably benign |
|
IGL03335:Carmil2
|
APN |
8 |
106,423,661 (GRCm39) |
missense |
probably benign |
0.14 |
Acubra
|
UTSW |
8 |
106,415,130 (GRCm39) |
nonsense |
probably null |
|
bowler
|
UTSW |
8 |
106,417,437 (GRCm39) |
missense |
probably damaging |
0.98 |
fedora
|
UTSW |
8 |
106,417,398 (GRCm39) |
missense |
possibly damaging |
0.88 |
fez
|
UTSW |
8 |
106,419,677 (GRCm39) |
missense |
probably damaging |
1.00 |
Panama
|
UTSW |
8 |
106,412,947 (GRCm39) |
critical splice donor site |
probably null |
|
R0544:Carmil2
|
UTSW |
8 |
106,417,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R2160:Carmil2
|
UTSW |
8 |
106,423,680 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2512:Carmil2
|
UTSW |
8 |
106,424,025 (GRCm39) |
missense |
probably benign |
0.31 |
R2877:Carmil2
|
UTSW |
8 |
106,422,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R2943:Carmil2
|
UTSW |
8 |
106,419,564 (GRCm39) |
missense |
probably benign |
0.17 |
R4038:Carmil2
|
UTSW |
8 |
106,422,039 (GRCm39) |
missense |
probably damaging |
0.99 |
R4615:Carmil2
|
UTSW |
8 |
106,421,706 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4914:Carmil2
|
UTSW |
8 |
106,420,175 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5106:Carmil2
|
UTSW |
8 |
106,420,638 (GRCm39) |
splice site |
probably null |
|
R5125:Carmil2
|
UTSW |
8 |
106,423,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5178:Carmil2
|
UTSW |
8 |
106,423,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5735:Carmil2
|
UTSW |
8 |
106,424,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R5991:Carmil2
|
UTSW |
8 |
106,418,023 (GRCm39) |
missense |
probably null |
1.00 |
R6035:Carmil2
|
UTSW |
8 |
106,419,195 (GRCm39) |
missense |
probably benign |
0.27 |
R6035:Carmil2
|
UTSW |
8 |
106,419,195 (GRCm39) |
missense |
probably benign |
0.27 |
R6226:Carmil2
|
UTSW |
8 |
106,415,664 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6411:Carmil2
|
UTSW |
8 |
106,423,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R7263:Carmil2
|
UTSW |
8 |
106,419,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R7368:Carmil2
|
UTSW |
8 |
106,417,467 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7409:Carmil2
|
UTSW |
8 |
106,419,423 (GRCm39) |
splice site |
probably null |
|
R7597:Carmil2
|
UTSW |
8 |
106,422,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R7674:Carmil2
|
UTSW |
8 |
106,423,918 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7759:Carmil2
|
UTSW |
8 |
106,423,668 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7864:Carmil2
|
UTSW |
8 |
106,414,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R7921:Carmil2
|
UTSW |
8 |
106,417,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R8057:Carmil2
|
UTSW |
8 |
106,419,008 (GRCm39) |
missense |
probably benign |
0.04 |
R8079:Carmil2
|
UTSW |
8 |
106,413,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Carmil2
|
UTSW |
8 |
106,416,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R8366:Carmil2
|
UTSW |
8 |
106,419,707 (GRCm39) |
missense |
probably benign |
0.02 |
R8453:Carmil2
|
UTSW |
8 |
106,416,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R8526:Carmil2
|
UTSW |
8 |
106,415,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Carmil2
|
UTSW |
8 |
106,412,947 (GRCm39) |
critical splice donor site |
probably null |
|
R8925:Carmil2
|
UTSW |
8 |
106,415,130 (GRCm39) |
nonsense |
probably null |
|
R8927:Carmil2
|
UTSW |
8 |
106,415,130 (GRCm39) |
nonsense |
probably null |
|
R8944:Carmil2
|
UTSW |
8 |
106,417,437 (GRCm39) |
missense |
probably damaging |
0.98 |
R8952:Carmil2
|
UTSW |
8 |
106,417,398 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9003:Carmil2
|
UTSW |
8 |
106,423,905 (GRCm39) |
missense |
probably damaging |
0.98 |
R9155:Carmil2
|
UTSW |
8 |
106,412,922 (GRCm39) |
missense |
probably benign |
0.12 |
R9318:Carmil2
|
UTSW |
8 |
106,414,486 (GRCm39) |
missense |
probably benign |
0.00 |
R9753:Carmil2
|
UTSW |
8 |
106,417,539 (GRCm39) |
missense |
probably damaging |
1.00 |
|