Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 110,039,706 (GRCm39) |
F436L |
probably damaging |
Het |
Adh6a |
A |
G |
3: 138,031,932 (GRCm39) |
T275A |
possibly damaging |
Het |
Agap2 |
A |
G |
10: 126,927,244 (GRCm39) |
D1082G |
possibly damaging |
Het |
Alox5 |
A |
T |
6: 116,400,150 (GRCm39) |
V263E |
probably damaging |
Het |
Arhgef16 |
C |
T |
4: 154,372,420 (GRCm39) |
|
probably null |
Het |
Bspry |
G |
A |
4: 62,404,762 (GRCm39) |
R186Q |
probably damaging |
Het |
Ccdc188 |
T |
A |
16: 18,036,159 (GRCm39) |
H111Q |
probably damaging |
Het |
Cd40 |
T |
C |
2: 164,911,615 (GRCm39) |
F209S |
possibly damaging |
Het |
Cfap43 |
C |
A |
19: 47,736,298 (GRCm39) |
V1398L |
probably benign |
Het |
Cln3 |
A |
T |
7: 126,174,565 (GRCm39) |
I286N |
possibly damaging |
Het |
Col9a1 |
T |
C |
1: 24,263,787 (GRCm39) |
|
probably null |
Het |
Cpne9 |
A |
G |
6: 113,279,016 (GRCm39) |
E470G |
probably damaging |
Het |
Cul5 |
A |
T |
9: 53,534,171 (GRCm39) |
W654R |
probably damaging |
Het |
Cyp2a22 |
T |
A |
7: 26,638,634 (GRCm39) |
K51* |
probably null |
Het |
Dcaf10 |
G |
A |
4: 45,372,769 (GRCm39) |
R394Q |
possibly damaging |
Het |
Dot1l |
C |
A |
10: 80,622,016 (GRCm39) |
S556* |
probably null |
Het |
Eif3d |
A |
T |
15: 77,851,516 (GRCm39) |
M98K |
probably benign |
Het |
Fiz1 |
A |
G |
7: 5,012,167 (GRCm39) |
V117A |
probably benign |
Het |
Fryl |
A |
G |
5: 73,257,636 (GRCm39) |
V722A |
probably benign |
Het |
Ftdc1 |
G |
A |
16: 58,434,333 (GRCm39) |
T128I |
probably benign |
Het |
Gm3095 |
G |
T |
14: 3,964,471 (GRCm38) |
R63I |
probably benign |
Het |
Gm7133 |
A |
T |
1: 97,197,224 (GRCm39) |
|
noncoding transcript |
Het |
Hoxb8 |
A |
T |
11: 96,175,286 (GRCm39) |
D241V |
probably benign |
Het |
Hrnr |
A |
G |
3: 93,230,959 (GRCm39) |
Q399R |
unknown |
Het |
Itpk1 |
A |
T |
12: 102,572,434 (GRCm39) |
V93D |
probably damaging |
Het |
Kars1 |
C |
T |
8: 112,729,216 (GRCm39) |
A164T |
probably benign |
Het |
Kcnq4 |
A |
T |
4: 120,574,208 (GRCm39) |
I150N |
probably damaging |
Het |
Kcnrg |
A |
T |
14: 61,849,176 (GRCm39) |
L212F |
probably damaging |
Het |
Kif5b |
A |
T |
18: 6,216,759 (GRCm39) |
D521E |
probably benign |
Het |
Klf11 |
C |
T |
12: 24,705,071 (GRCm39) |
T158M |
probably damaging |
Het |
Klhl6 |
T |
C |
16: 19,776,034 (GRCm39) |
I175V |
probably benign |
Het |
Lsm1 |
A |
G |
8: 26,283,708 (GRCm39) |
N40S |
probably damaging |
Het |
Map1b |
T |
C |
13: 99,567,576 (GRCm39) |
E1715G |
unknown |
Het |
Mecom |
C |
A |
3: 30,292,459 (GRCm39) |
A4S |
probably benign |
Het |
Muc5b |
G |
A |
7: 141,396,031 (GRCm39) |
V96M |
unknown |
Het |
Mug2 |
A |
T |
6: 122,013,255 (GRCm39) |
I341L |
probably benign |
Het |
Mxra7 |
A |
T |
11: 116,707,078 (GRCm39) |
|
probably null |
Het |
Myo5a |
T |
C |
9: 75,061,105 (GRCm39) |
L537P |
probably damaging |
Het |
Myo5b |
A |
T |
18: 74,855,533 (GRCm39) |
N1241Y |
probably damaging |
Het |
Naa16 |
T |
C |
14: 79,582,497 (GRCm39) |
R531G |
probably damaging |
Het |
Neb |
T |
A |
2: 52,134,087 (GRCm39) |
M3299L |
probably benign |
Het |
Nlrp4b |
T |
A |
7: 10,453,130 (GRCm39) |
Y76N |
probably benign |
Het |
Nmral1 |
T |
C |
16: 4,534,205 (GRCm39) |
T79A |
probably damaging |
Het |
Noct |
C |
T |
3: 51,155,300 (GRCm39) |
Q23* |
probably null |
Het |
Nrxn1 |
A |
T |
17: 90,344,509 (GRCm39) |
V438D |
probably damaging |
Het |
Or5b109 |
A |
C |
19: 13,212,132 (GRCm39) |
N173H |
possibly damaging |
Het |
Or5m9 |
T |
A |
2: 85,877,242 (GRCm39) |
C139S |
probably damaging |
Het |
Oxct2a |
T |
C |
4: 123,216,836 (GRCm39) |
T182A |
probably benign |
Het |
Pank2 |
T |
C |
2: 131,115,945 (GRCm39) |
I121T |
probably damaging |
Het |
Pcdh1 |
T |
A |
18: 38,336,528 (GRCm39) |
T36S |
probably benign |
Het |
Pfdn1 |
A |
T |
18: 36,584,133 (GRCm39) |
M67K |
possibly damaging |
Het |
Plec |
T |
C |
15: 76,058,456 (GRCm39) |
E3849G |
probably damaging |
Het |
Polr3a |
A |
T |
14: 24,514,349 (GRCm39) |
S817T |
possibly damaging |
Het |
Pomgnt1 |
T |
A |
4: 116,012,707 (GRCm39) |
D401E |
probably damaging |
Het |
Ppp1r13b |
T |
A |
12: 111,798,992 (GRCm39) |
D891V |
probably damaging |
Het |
Prr14l |
A |
G |
5: 33,001,500 (GRCm39) |
|
probably benign |
Het |
Ptk2b |
A |
G |
14: 66,410,749 (GRCm39) |
|
probably null |
Het |
Rab13 |
G |
C |
3: 90,128,330 (GRCm39) |
|
probably null |
Het |
Rexo1 |
C |
T |
10: 80,382,255 (GRCm39) |
A751T |
probably benign |
Het |
Rfx1 |
T |
C |
8: 84,809,374 (GRCm39) |
V233A |
possibly damaging |
Het |
Rnf149 |
C |
T |
1: 39,616,295 (GRCm39) |
|
probably benign |
Het |
Rrm1 |
A |
G |
7: 102,097,086 (GRCm39) |
D122G |
probably benign |
Het |
Serpina1b |
A |
G |
12: 103,698,639 (GRCm39) |
F70S |
probably damaging |
Het |
Serpinb13 |
C |
T |
1: 106,910,574 (GRCm39) |
S66L |
probably damaging |
Het |
Sh3rf3 |
T |
C |
10: 58,649,526 (GRCm39) |
S44P |
possibly damaging |
Het |
Shroom1 |
A |
G |
11: 53,356,549 (GRCm39) |
T471A |
possibly damaging |
Het |
Slc6a1 |
A |
G |
6: 114,279,792 (GRCm39) |
Y152C |
probably damaging |
Het |
Spata31f3 |
T |
A |
4: 42,873,032 (GRCm39) |
|
probably null |
Het |
Spata6 |
A |
T |
4: 111,632,023 (GRCm39) |
T145S |
probably damaging |
Het |
Srcap |
G |
A |
7: 127,137,186 (GRCm39) |
G956D |
probably damaging |
Het |
Ssh2 |
A |
T |
11: 77,346,031 (GRCm39) |
I1339F |
possibly damaging |
Het |
Tardbp |
A |
T |
4: 148,697,078 (GRCm39) |
*99K |
probably null |
Het |
Tbc1d22a |
A |
G |
15: 86,196,037 (GRCm39) |
Y336C |
probably damaging |
Het |
Tmcc3 |
G |
A |
10: 94,381,419 (GRCm39) |
|
probably benign |
Het |
Tmem178b |
T |
G |
6: 40,222,547 (GRCm39) |
D87E |
probably benign |
Het |
Tmem184a |
A |
C |
5: 139,791,377 (GRCm39) |
S380A |
probably benign |
Het |
Tnfaip2 |
A |
G |
12: 111,411,682 (GRCm39) |
K84R |
possibly damaging |
Het |
Tpgs1 |
A |
G |
10: 79,511,235 (GRCm39) |
T126A |
probably benign |
Het |
Traf3ip1 |
A |
G |
1: 91,447,834 (GRCm39) |
E437G |
possibly damaging |
Het |
Trpc4ap |
C |
T |
2: 155,477,053 (GRCm39) |
C755Y |
probably damaging |
Het |
Tsfm |
A |
G |
10: 126,866,547 (GRCm39) |
|
probably benign |
Het |
Tulp1 |
A |
C |
17: 28,570,811 (GRCm39) |
|
probably benign |
Het |
Vmn1r23 |
A |
T |
6: 57,903,010 (GRCm39) |
M256K |
probably benign |
Het |
Zdhhc8 |
T |
C |
16: 18,044,605 (GRCm39) |
D305G |
probably damaging |
Het |
Zfp326 |
G |
A |
5: 106,054,942 (GRCm39) |
R282H |
probably damaging |
Het |
|
Other mutations in Adam28 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Adam28
|
APN |
14 |
68,859,569 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL00654:Adam28
|
APN |
14 |
68,886,877 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01021:Adam28
|
APN |
14 |
68,879,563 (GRCm39) |
missense |
probably benign |
|
IGL01099:Adam28
|
APN |
14 |
68,874,778 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01349:Adam28
|
APN |
14 |
68,848,455 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01744:Adam28
|
APN |
14 |
68,844,956 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01805:Adam28
|
APN |
14 |
68,879,540 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02007:Adam28
|
APN |
14 |
68,870,668 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02828:Adam28
|
APN |
14 |
68,884,319 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL03180:Adam28
|
APN |
14 |
68,874,883 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03355:Adam28
|
APN |
14 |
68,872,252 (GRCm39) |
splice site |
probably benign |
|
IGL02980:Adam28
|
UTSW |
14 |
68,857,255 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4453001:Adam28
|
UTSW |
14 |
68,872,325 (GRCm39) |
missense |
probably benign |
0.00 |
R0184:Adam28
|
UTSW |
14 |
68,874,822 (GRCm39) |
missense |
probably benign |
0.33 |
R0321:Adam28
|
UTSW |
14 |
68,855,200 (GRCm39) |
missense |
probably damaging |
0.97 |
R0329:Adam28
|
UTSW |
14 |
68,855,188 (GRCm39) |
missense |
probably damaging |
0.96 |
R0494:Adam28
|
UTSW |
14 |
68,868,241 (GRCm39) |
splice site |
probably benign |
|
R0605:Adam28
|
UTSW |
14 |
68,844,049 (GRCm39) |
unclassified |
probably benign |
|
R0732:Adam28
|
UTSW |
14 |
68,874,796 (GRCm39) |
missense |
probably benign |
0.00 |
R0959:Adam28
|
UTSW |
14 |
68,845,387 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1319:Adam28
|
UTSW |
14 |
68,846,578 (GRCm39) |
missense |
probably benign |
0.28 |
R1745:Adam28
|
UTSW |
14 |
68,870,620 (GRCm39) |
missense |
probably benign |
0.04 |
R1836:Adam28
|
UTSW |
14 |
68,886,870 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1838:Adam28
|
UTSW |
14 |
68,876,659 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1839:Adam28
|
UTSW |
14 |
68,876,659 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1850:Adam28
|
UTSW |
14 |
68,876,644 (GRCm39) |
missense |
probably benign |
0.01 |
R1912:Adam28
|
UTSW |
14 |
68,881,780 (GRCm39) |
missense |
probably benign |
0.24 |
R2830:Adam28
|
UTSW |
14 |
68,864,363 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2889:Adam28
|
UTSW |
14 |
68,872,294 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3977:Adam28
|
UTSW |
14 |
68,848,443 (GRCm39) |
missense |
probably benign |
0.20 |
R3978:Adam28
|
UTSW |
14 |
68,848,443 (GRCm39) |
missense |
probably benign |
0.20 |
R3979:Adam28
|
UTSW |
14 |
68,848,443 (GRCm39) |
missense |
probably benign |
0.20 |
R4282:Adam28
|
UTSW |
14 |
68,885,155 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4416:Adam28
|
UTSW |
14 |
68,859,531 (GRCm39) |
critical splice donor site |
probably null |
|
R4724:Adam28
|
UTSW |
14 |
68,864,326 (GRCm39) |
missense |
probably damaging |
0.99 |
R4768:Adam28
|
UTSW |
14 |
68,872,264 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4883:Adam28
|
UTSW |
14 |
68,875,552 (GRCm39) |
missense |
probably damaging |
0.99 |
R5054:Adam28
|
UTSW |
14 |
68,855,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R5710:Adam28
|
UTSW |
14 |
68,847,357 (GRCm39) |
missense |
probably damaging |
0.96 |
R5835:Adam28
|
UTSW |
14 |
68,893,130 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6002:Adam28
|
UTSW |
14 |
68,879,511 (GRCm39) |
missense |
probably benign |
|
R6054:Adam28
|
UTSW |
14 |
68,879,601 (GRCm39) |
missense |
probably benign |
0.01 |
R6349:Adam28
|
UTSW |
14 |
68,870,621 (GRCm39) |
missense |
probably benign |
0.29 |
R6449:Adam28
|
UTSW |
14 |
68,868,116 (GRCm39) |
missense |
probably benign |
0.31 |
R6455:Adam28
|
UTSW |
14 |
68,870,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R6831:Adam28
|
UTSW |
14 |
68,855,576 (GRCm39) |
missense |
probably benign |
0.04 |
R6833:Adam28
|
UTSW |
14 |
68,855,576 (GRCm39) |
missense |
probably benign |
0.04 |
R7212:Adam28
|
UTSW |
14 |
68,874,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R7411:Adam28
|
UTSW |
14 |
68,864,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Adam28
|
UTSW |
14 |
68,864,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R7516:Adam28
|
UTSW |
14 |
68,868,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R7649:Adam28
|
UTSW |
14 |
68,872,282 (GRCm39) |
missense |
probably benign |
0.12 |
R7765:Adam28
|
UTSW |
14 |
68,846,555 (GRCm39) |
critical splice donor site |
probably null |
|
R8469:Adam28
|
UTSW |
14 |
68,844,029 (GRCm39) |
missense |
probably benign |
0.16 |
R8520:Adam28
|
UTSW |
14 |
68,879,532 (GRCm39) |
missense |
probably damaging |
0.98 |
R9026:Adam28
|
UTSW |
14 |
68,846,593 (GRCm39) |
missense |
probably benign |
0.16 |
R9163:Adam28
|
UTSW |
14 |
68,866,531 (GRCm39) |
missense |
probably damaging |
0.98 |
R9264:Adam28
|
UTSW |
14 |
68,844,914 (GRCm39) |
missense |
probably benign |
|
R9304:Adam28
|
UTSW |
14 |
68,874,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R9357:Adam28
|
UTSW |
14 |
68,879,479 (GRCm39) |
missense |
probably benign |
0.36 |
R9441:Adam28
|
UTSW |
14 |
68,874,943 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Adam28
|
UTSW |
14 |
68,864,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|