Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
A |
T |
5: 8,989,885 (GRCm39) |
R813* |
probably null |
Het |
Accsl |
T |
A |
2: 93,696,419 (GRCm39) |
I60F |
probably benign |
Het |
Ankrd13c |
A |
G |
3: 157,697,351 (GRCm39) |
I319V |
probably benign |
Het |
Bag6 |
T |
G |
17: 35,360,442 (GRCm39) |
V327G |
probably damaging |
Het |
Barhl1 |
C |
T |
2: 28,805,304 (GRCm39) |
A130T |
probably benign |
Het |
Bend4 |
T |
C |
5: 67,555,583 (GRCm39) |
D541G |
probably damaging |
Het |
Birc6 |
A |
C |
17: 74,999,290 (GRCm39) |
T4673P |
probably damaging |
Het |
Ccdc81 |
T |
C |
7: 89,539,679 (GRCm39) |
R186G |
probably damaging |
Het |
Cdyl2 |
A |
G |
8: 117,309,931 (GRCm39) |
F342L |
probably damaging |
Het |
Chd3 |
C |
A |
11: 69,248,367 (GRCm39) |
V748L |
probably damaging |
Het |
CN725425 |
G |
T |
15: 91,123,147 (GRCm39) |
R72I |
possibly damaging |
Het |
Col22a1 |
A |
G |
15: 71,834,520 (GRCm39) |
|
probably null |
Het |
Cops3 |
A |
G |
11: 59,709,243 (GRCm39) |
|
probably null |
Het |
Ctnnd1 |
G |
T |
2: 84,433,606 (GRCm39) |
Q940K |
possibly damaging |
Het |
Dtnb |
C |
T |
12: 3,641,971 (GRCm39) |
Q45* |
probably null |
Het |
Efr3a |
T |
A |
15: 65,714,553 (GRCm39) |
I280K |
probably damaging |
Het |
Eml6 |
A |
C |
11: 29,843,213 (GRCm39) |
V167G |
probably benign |
Het |
Fam83c |
T |
A |
2: 155,672,215 (GRCm39) |
M407L |
probably benign |
Het |
Fasn |
T |
C |
11: 120,701,894 (GRCm39) |
T1862A |
probably benign |
Het |
Fbxl6 |
A |
G |
15: 76,420,155 (GRCm39) |
I486T |
probably damaging |
Het |
Gpr182 |
A |
G |
10: 127,586,565 (GRCm39) |
Y129H |
probably damaging |
Het |
Gpr75 |
A |
G |
11: 30,842,456 (GRCm39) |
S454G |
probably damaging |
Het |
Hectd4 |
G |
A |
5: 121,502,653 (GRCm39) |
|
probably null |
Het |
Hsf4 |
A |
G |
8: 106,002,222 (GRCm39) |
T411A |
probably benign |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Il4 |
A |
T |
11: 53,509,432 (GRCm39) |
M1K |
probably null |
Het |
Ints11 |
G |
T |
4: 155,972,405 (GRCm39) |
R463L |
probably benign |
Het |
Ints4 |
G |
A |
7: 97,178,430 (GRCm39) |
E677K |
probably damaging |
Het |
Klk1b11 |
G |
A |
7: 43,647,216 (GRCm39) |
C50Y |
probably damaging |
Het |
Krt14 |
C |
A |
11: 100,098,221 (GRCm39) |
G21C |
unknown |
Het |
Krt81 |
C |
A |
15: 101,361,508 (GRCm39) |
R24L |
possibly damaging |
Het |
L3mbtl2 |
C |
T |
15: 81,552,942 (GRCm39) |
A125V |
probably damaging |
Het |
Lama3 |
A |
G |
18: 12,633,569 (GRCm39) |
|
probably null |
Het |
Lrrk2 |
T |
C |
15: 91,634,478 (GRCm39) |
L1414P |
probably damaging |
Het |
Matn2 |
T |
C |
15: 34,428,687 (GRCm39) |
S684P |
probably damaging |
Het |
Mga |
T |
A |
2: 119,771,862 (GRCm39) |
V1574D |
probably damaging |
Het |
Mia2 |
T |
C |
12: 59,219,380 (GRCm39) |
|
probably null |
Het |
Mrpl21 |
T |
A |
19: 3,342,459 (GRCm39) |
|
probably benign |
Het |
Msh5 |
T |
A |
17: 35,260,458 (GRCm39) |
Q266L |
probably benign |
Het |
Mybpc1 |
C |
A |
10: 88,376,822 (GRCm39) |
C758F |
probably damaging |
Het |
Myo15a |
G |
A |
11: 60,400,422 (GRCm39) |
A2932T |
possibly damaging |
Het |
Nbas |
T |
A |
12: 13,569,109 (GRCm39) |
I2021K |
probably benign |
Het |
Neurl4 |
T |
C |
11: 69,796,393 (GRCm39) |
S424P |
probably damaging |
Het |
Or10j5 |
T |
A |
1: 172,784,965 (GRCm39) |
V201E |
probably damaging |
Het |
Or2w3 |
A |
C |
11: 58,556,789 (GRCm39) |
I135L |
probably benign |
Het |
Or6c6 |
A |
G |
10: 129,187,103 (GRCm39) |
M224V |
probably benign |
Het |
Or7g17 |
T |
C |
9: 18,767,945 (GRCm39) |
M8T |
probably benign |
Het |
Or7g32 |
T |
A |
9: 19,389,388 (GRCm39) |
I53F |
possibly damaging |
Het |
Phlpp1 |
C |
T |
1: 106,278,308 (GRCm39) |
R907W |
probably damaging |
Het |
Pigg |
T |
C |
5: 108,484,277 (GRCm39) |
V508A |
probably benign |
Het |
Pkhd1l1 |
T |
G |
15: 44,364,915 (GRCm39) |
Y685D |
probably damaging |
Het |
Polr3a |
A |
T |
14: 24,534,534 (GRCm39) |
I34N |
probably damaging |
Het |
Pramel17 |
T |
C |
4: 101,694,158 (GRCm39) |
S242G |
probably benign |
Het |
Prex1 |
A |
G |
2: 166,411,297 (GRCm39) |
V1434A |
probably benign |
Het |
Ptprh |
T |
A |
7: 4,601,005 (GRCm39) |
D124V |
probably damaging |
Het |
Rad54b |
T |
A |
4: 11,606,131 (GRCm39) |
I513N |
probably benign |
Het |
Rbm12b1 |
A |
G |
4: 12,145,507 (GRCm39) |
N493S |
probably benign |
Het |
Rfx7 |
A |
T |
9: 72,517,586 (GRCm39) |
|
probably null |
Het |
Serpini1 |
A |
G |
3: 75,520,648 (GRCm39) |
K82E |
probably benign |
Het |
Slc27a6 |
T |
G |
18: 58,742,237 (GRCm39) |
|
probably null |
Het |
Slc35f2 |
G |
T |
9: 53,724,201 (GRCm39) |
L358F |
probably damaging |
Het |
Slc45a1 |
A |
C |
4: 150,727,762 (GRCm39) |
I158M |
probably damaging |
Het |
Slurp2 |
G |
A |
15: 74,614,955 (GRCm39) |
P62L |
probably damaging |
Het |
Sspo |
C |
T |
6: 48,443,674 (GRCm39) |
H1949Y |
probably damaging |
Het |
Tiam1 |
A |
T |
16: 89,634,715 (GRCm39) |
V865E |
possibly damaging |
Het |
Tlr4 |
A |
C |
4: 66,757,857 (GRCm39) |
I217L |
probably damaging |
Het |
Top1 |
C |
T |
2: 160,554,628 (GRCm39) |
R460* |
probably null |
Het |
Trpm3 |
T |
A |
19: 22,965,418 (GRCm39) |
S1638T |
probably benign |
Het |
Tubgcp5 |
C |
T |
7: 55,473,315 (GRCm39) |
R798C |
probably benign |
Het |
Vars1 |
T |
G |
17: 35,231,703 (GRCm39) |
|
probably null |
Het |
Xylt2 |
A |
G |
11: 94,557,159 (GRCm39) |
Y111H |
probably benign |
Het |
Zbed5 |
G |
A |
5: 129,930,567 (GRCm39) |
G172D |
probably damaging |
Het |
Zfp53 |
C |
T |
17: 21,729,095 (GRCm39) |
T376I |
probably benign |
Het |
Zfp937 |
G |
T |
2: 150,081,466 (GRCm39) |
V499L |
probably benign |
Het |
Zyx |
T |
A |
6: 42,328,247 (GRCm39) |
L152Q |
probably damaging |
Het |
|
Other mutations in Adam29 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01305:Adam29
|
APN |
8 |
56,324,879 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01406:Adam29
|
APN |
8 |
56,324,874 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01511:Adam29
|
APN |
8 |
56,324,456 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01869:Adam29
|
APN |
8 |
56,324,732 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01894:Adam29
|
APN |
8 |
56,324,865 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02023:Adam29
|
APN |
8 |
56,325,519 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02030:Adam29
|
APN |
8 |
56,325,157 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02071:Adam29
|
APN |
8 |
56,324,589 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02094:Adam29
|
APN |
8 |
56,324,480 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02108:Adam29
|
APN |
8 |
56,325,346 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02125:Adam29
|
APN |
8 |
56,324,974 (GRCm39) |
nonsense |
probably null |
|
IGL02330:Adam29
|
APN |
8 |
56,325,398 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02332:Adam29
|
APN |
8 |
56,324,775 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02548:Adam29
|
APN |
8 |
56,325,902 (GRCm39) |
nonsense |
probably null |
|
IGL02960:Adam29
|
APN |
8 |
56,325,701 (GRCm39) |
nonsense |
probably null |
|
IGL03030:Adam29
|
APN |
8 |
56,326,100 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU22:Adam29
|
UTSW |
8 |
56,324,879 (GRCm39) |
missense |
probably benign |
0.01 |
D4043:Adam29
|
UTSW |
8 |
56,325,496 (GRCm39) |
nonsense |
probably null |
|
IGL02835:Adam29
|
UTSW |
8 |
56,326,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R0294:Adam29
|
UTSW |
8 |
56,326,311 (GRCm39) |
missense |
probably benign |
0.25 |
R0607:Adam29
|
UTSW |
8 |
56,326,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:Adam29
|
UTSW |
8 |
56,324,612 (GRCm39) |
missense |
probably benign |
0.24 |
R1296:Adam29
|
UTSW |
8 |
56,324,754 (GRCm39) |
nonsense |
probably null |
|
R1752:Adam29
|
UTSW |
8 |
56,325,309 (GRCm39) |
missense |
probably damaging |
0.98 |
R1930:Adam29
|
UTSW |
8 |
56,326,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R1931:Adam29
|
UTSW |
8 |
56,326,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R2397:Adam29
|
UTSW |
8 |
56,325,933 (GRCm39) |
missense |
probably benign |
0.04 |
R2764:Adam29
|
UTSW |
8 |
56,324,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R4052:Adam29
|
UTSW |
8 |
56,325,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R4978:Adam29
|
UTSW |
8 |
56,324,436 (GRCm39) |
missense |
probably damaging |
0.98 |
R5306:Adam29
|
UTSW |
8 |
56,324,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R6383:Adam29
|
UTSW |
8 |
56,324,543 (GRCm39) |
missense |
probably damaging |
0.99 |
R6528:Adam29
|
UTSW |
8 |
56,325,596 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6579:Adam29
|
UTSW |
8 |
56,325,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R6707:Adam29
|
UTSW |
8 |
56,325,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R7076:Adam29
|
UTSW |
8 |
56,324,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R7099:Adam29
|
UTSW |
8 |
56,324,439 (GRCm39) |
missense |
probably benign |
0.01 |
R7177:Adam29
|
UTSW |
8 |
56,325,659 (GRCm39) |
missense |
probably benign |
0.30 |
R7320:Adam29
|
UTSW |
8 |
56,325,749 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7420:Adam29
|
UTSW |
8 |
56,325,933 (GRCm39) |
missense |
probably benign |
0.04 |
R7438:Adam29
|
UTSW |
8 |
56,324,609 (GRCm39) |
missense |
probably damaging |
0.99 |
R7476:Adam29
|
UTSW |
8 |
56,326,230 (GRCm39) |
missense |
probably damaging |
0.97 |
R7524:Adam29
|
UTSW |
8 |
56,325,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R8066:Adam29
|
UTSW |
8 |
56,325,703 (GRCm39) |
missense |
probably benign |
0.11 |
R8111:Adam29
|
UTSW |
8 |
56,324,585 (GRCm39) |
missense |
probably benign |
0.00 |
R8221:Adam29
|
UTSW |
8 |
56,325,463 (GRCm39) |
missense |
probably benign |
0.02 |
R8350:Adam29
|
UTSW |
8 |
56,325,224 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8353:Adam29
|
UTSW |
8 |
56,326,196 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8453:Adam29
|
UTSW |
8 |
56,326,196 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8723:Adam29
|
UTSW |
8 |
56,324,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R8752:Adam29
|
UTSW |
8 |
56,325,328 (GRCm39) |
nonsense |
probably null |
|
R8809:Adam29
|
UTSW |
8 |
56,325,659 (GRCm39) |
missense |
probably benign |
0.30 |
R9025:Adam29
|
UTSW |
8 |
56,325,196 (GRCm39) |
nonsense |
probably null |
|
R9388:Adam29
|
UTSW |
8 |
56,325,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R9612:Adam29
|
UTSW |
8 |
56,325,118 (GRCm39) |
missense |
possibly damaging |
0.77 |
X0011:Adam29
|
UTSW |
8 |
56,326,203 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Adam29
|
UTSW |
8 |
56,324,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|