Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adhfe1 |
G |
A |
1: 9,623,698 (GRCm39) |
|
probably null |
Het |
Adsl |
C |
T |
15: 80,836,425 (GRCm39) |
Q61* |
probably null |
Het |
Arhgap26 |
T |
A |
18: 39,429,925 (GRCm39) |
C214S |
probably damaging |
Het |
Armc8 |
A |
T |
9: 99,419,782 (GRCm39) |
N9K |
probably damaging |
Het |
Asxl1 |
A |
G |
2: 153,242,375 (GRCm39) |
D975G |
probably damaging |
Het |
Atp8b3 |
T |
C |
10: 80,368,412 (GRCm39) |
E187G |
probably damaging |
Het |
Bltp1 |
G |
A |
3: 36,996,548 (GRCm39) |
D1087N |
probably damaging |
Het |
Cdcp2 |
T |
C |
4: 106,959,710 (GRCm39) |
S42P |
probably damaging |
Het |
Chek1 |
A |
G |
9: 36,630,820 (GRCm39) |
L198P |
probably damaging |
Het |
Dlc1 |
A |
G |
8: 37,317,406 (GRCm39) |
V423A |
probably benign |
Het |
Dpy19l2 |
A |
G |
9: 24,492,511 (GRCm39) |
S696P |
probably benign |
Het |
Echdc3 |
A |
T |
2: 6,200,438 (GRCm39) |
C183S |
possibly damaging |
Het |
Exph5 |
A |
C |
9: 53,285,595 (GRCm39) |
D892A |
probably benign |
Het |
Fam120b |
T |
A |
17: 15,622,073 (GRCm39) |
I17K |
possibly damaging |
Het |
Fbln5 |
C |
T |
12: 101,731,457 (GRCm39) |
D246N |
probably benign |
Het |
Fbxo15 |
A |
C |
18: 84,980,745 (GRCm39) |
K195T |
possibly damaging |
Het |
Fzd1 |
C |
A |
5: 4,807,514 (GRCm39) |
E23* |
probably null |
Het |
Gas2l1 |
C |
A |
11: 5,014,434 (GRCm39) |
A9S |
probably damaging |
Het |
Gcc2 |
C |
T |
10: 58,105,270 (GRCm39) |
L69F |
probably damaging |
Het |
Ggt6 |
C |
T |
11: 72,328,559 (GRCm39) |
A353V |
possibly damaging |
Het |
Gphn |
T |
A |
12: 78,730,657 (GRCm39) |
V764E |
probably damaging |
Het |
Grid1 |
A |
T |
14: 35,167,922 (GRCm39) |
Y482F |
probably damaging |
Het |
Hlx |
G |
T |
1: 184,464,184 (GRCm39) |
A52D |
probably damaging |
Het |
Ifit1bl1 |
C |
T |
19: 34,571,444 (GRCm39) |
V338M |
probably benign |
Het |
Klhl14 |
T |
A |
18: 21,698,589 (GRCm39) |
Q408L |
possibly damaging |
Het |
Lacc1 |
T |
A |
14: 77,267,081 (GRCm39) |
Q394L |
probably benign |
Het |
Lcor |
T |
G |
19: 41,573,513 (GRCm39) |
M756R |
probably benign |
Het |
Lipe |
A |
G |
7: 25,087,569 (GRCm39) |
F477L |
probably damaging |
Het |
Lrig2 |
A |
G |
3: 104,387,423 (GRCm39) |
|
probably null |
Het |
Megf8 |
T |
A |
7: 25,058,120 (GRCm39) |
H2131Q |
probably damaging |
Het |
Nek1 |
A |
G |
8: 61,577,310 (GRCm39) |
D1097G |
possibly damaging |
Het |
Nhlrc3 |
A |
T |
3: 53,366,078 (GRCm39) |
Y138* |
probably null |
Het |
Nudcd2 |
T |
A |
11: 40,626,834 (GRCm39) |
|
probably null |
Het |
Numb |
T |
C |
12: 83,847,784 (GRCm39) |
|
probably null |
Het |
Or7h8 |
T |
G |
9: 20,124,242 (GRCm39) |
L199R |
probably benign |
Het |
Pacrg |
G |
A |
17: 11,058,725 (GRCm39) |
Q11* |
probably null |
Het |
Ppp1r37 |
A |
T |
7: 19,268,924 (GRCm39) |
M192K |
probably damaging |
Het |
Prmt8 |
T |
A |
6: 127,666,799 (GRCm39) |
K392* |
probably null |
Het |
Rab28 |
A |
T |
5: 41,855,795 (GRCm39) |
W67R |
probably damaging |
Het |
Rad21l |
C |
T |
2: 151,496,606 (GRCm39) |
C365Y |
probably damaging |
Het |
Rbm17 |
A |
T |
2: 11,600,208 (GRCm39) |
F147I |
probably benign |
Het |
Rbm46 |
A |
C |
3: 82,771,848 (GRCm39) |
F256V |
probably damaging |
Het |
Rcc1 |
A |
T |
4: 132,062,087 (GRCm39) |
|
probably null |
Het |
Rnf217 |
G |
T |
10: 31,410,807 (GRCm39) |
T296N |
possibly damaging |
Het |
Rnmt |
A |
G |
18: 68,444,724 (GRCm39) |
D231G |
possibly damaging |
Het |
Rph3al |
C |
T |
11: 75,797,367 (GRCm39) |
V110I |
probably damaging |
Het |
Rxfp2 |
T |
C |
5: 149,983,362 (GRCm39) |
M289T |
probably benign |
Het |
Sash1 |
T |
C |
10: 8,605,721 (GRCm39) |
R890G |
probably benign |
Het |
Sf3b2 |
A |
T |
19: 5,338,026 (GRCm39) |
D245E |
probably benign |
Het |
Skint9 |
A |
T |
4: 112,246,398 (GRCm39) |
V238E |
probably benign |
Het |
Slc26a8 |
T |
A |
17: 28,857,455 (GRCm39) |
D896V |
possibly damaging |
Het |
Slc35b4 |
T |
A |
6: 34,135,323 (GRCm39) |
K330* |
probably null |
Het |
Slco1a4 |
G |
T |
6: 141,785,337 (GRCm39) |
H84Q |
probably damaging |
Het |
Sptbn2 |
G |
T |
19: 4,800,270 (GRCm39) |
|
probably null |
Het |
St6galnac3 |
A |
T |
3: 152,912,305 (GRCm39) |
D227E |
probably benign |
Het |
Tek |
G |
A |
4: 94,738,004 (GRCm39) |
D685N |
probably damaging |
Het |
Trf |
G |
T |
9: 103,102,335 (GRCm39) |
|
probably null |
Het |
Trpm5 |
T |
A |
7: 142,638,908 (GRCm39) |
K288* |
probably null |
Het |
Ttn |
C |
T |
2: 76,567,356 (GRCm39) |
V27846I |
probably damaging |
Het |
Tyr |
A |
T |
7: 87,087,179 (GRCm39) |
D444E |
probably benign |
Het |
Ucp1 |
C |
A |
8: 84,021,933 (GRCm39) |
A255E |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,491,963 (GRCm39) |
D3084G |
probably benign |
Het |
Yeats4 |
T |
C |
10: 117,053,344 (GRCm39) |
Y139C |
probably damaging |
Het |
Zbtb6 |
A |
G |
2: 37,319,130 (GRCm39) |
V266A |
probably benign |
Het |
Zfp784 |
A |
T |
7: 5,038,774 (GRCm39) |
N261K |
possibly damaging |
Het |
|
Other mutations in Abcc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00430:Abcc2
|
APN |
19 |
43,772,641 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01611:Abcc2
|
APN |
19 |
43,815,068 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01800:Abcc2
|
APN |
19 |
43,772,734 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02008:Abcc2
|
APN |
19 |
43,810,189 (GRCm39) |
splice site |
probably benign |
|
IGL02041:Abcc2
|
APN |
19 |
43,772,674 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02528:Abcc2
|
APN |
19 |
43,786,943 (GRCm39) |
missense |
probably benign |
|
IGL02950:Abcc2
|
APN |
19 |
43,814,406 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03081:Abcc2
|
APN |
19 |
43,770,841 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03397:Abcc2
|
APN |
19 |
43,772,743 (GRCm39) |
missense |
probably benign |
0.00 |
loser
|
UTSW |
19 |
43,827,850 (GRCm39) |
utr 3 prime |
probably benign |
|
nelson
|
UTSW |
19 |
43,792,178 (GRCm39) |
missense |
probably benign |
0.07 |
Sore
|
UTSW |
19 |
43,786,633 (GRCm39) |
missense |
probably benign |
0.22 |
BB002:Abcc2
|
UTSW |
19 |
43,795,551 (GRCm39) |
missense |
probably benign |
0.07 |
BB012:Abcc2
|
UTSW |
19 |
43,795,551 (GRCm39) |
missense |
probably benign |
0.07 |
PIT4453001:Abcc2
|
UTSW |
19 |
43,792,221 (GRCm39) |
nonsense |
probably null |
|
PIT4519001:Abcc2
|
UTSW |
19 |
43,807,836 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0197:Abcc2
|
UTSW |
19 |
43,815,053 (GRCm39) |
nonsense |
probably null |
|
R0326:Abcc2
|
UTSW |
19 |
43,814,386 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0391:Abcc2
|
UTSW |
19 |
43,810,044 (GRCm39) |
splice site |
probably benign |
|
R0558:Abcc2
|
UTSW |
19 |
43,789,163 (GRCm39) |
missense |
probably benign |
0.00 |
R0577:Abcc2
|
UTSW |
19 |
43,807,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R0787:Abcc2
|
UTSW |
19 |
43,786,955 (GRCm39) |
critical splice donor site |
probably null |
|
R1189:Abcc2
|
UTSW |
19 |
43,807,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R1200:Abcc2
|
UTSW |
19 |
43,822,426 (GRCm39) |
missense |
probably damaging |
0.98 |
R1395:Abcc2
|
UTSW |
19 |
43,822,379 (GRCm39) |
missense |
probably benign |
0.22 |
R1775:Abcc2
|
UTSW |
19 |
43,786,858 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1797:Abcc2
|
UTSW |
19 |
43,822,426 (GRCm39) |
missense |
probably damaging |
0.98 |
R1797:Abcc2
|
UTSW |
19 |
43,803,225 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1826:Abcc2
|
UTSW |
19 |
43,810,453 (GRCm39) |
missense |
probably benign |
0.01 |
R1882:Abcc2
|
UTSW |
19 |
43,786,945 (GRCm39) |
missense |
probably benign |
0.00 |
R1913:Abcc2
|
UTSW |
19 |
43,795,683 (GRCm39) |
missense |
probably benign |
0.10 |
R1986:Abcc2
|
UTSW |
19 |
43,818,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Abcc2
|
UTSW |
19 |
43,795,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R1992:Abcc2
|
UTSW |
19 |
43,795,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R2006:Abcc2
|
UTSW |
19 |
43,793,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R2057:Abcc2
|
UTSW |
19 |
43,806,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R3709:Abcc2
|
UTSW |
19 |
43,786,885 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3802:Abcc2
|
UTSW |
19 |
43,810,065 (GRCm39) |
missense |
probably benign |
0.01 |
R4010:Abcc2
|
UTSW |
19 |
43,818,303 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4014:Abcc2
|
UTSW |
19 |
43,811,559 (GRCm39) |
missense |
probably benign |
|
R4064:Abcc2
|
UTSW |
19 |
43,793,432 (GRCm39) |
nonsense |
probably null |
|
R4296:Abcc2
|
UTSW |
19 |
43,811,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R4296:Abcc2
|
UTSW |
19 |
43,811,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R4363:Abcc2
|
UTSW |
19 |
43,787,575 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4580:Abcc2
|
UTSW |
19 |
43,799,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R4625:Abcc2
|
UTSW |
19 |
43,792,178 (GRCm39) |
missense |
probably benign |
0.07 |
R4631:Abcc2
|
UTSW |
19 |
43,803,146 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4671:Abcc2
|
UTSW |
19 |
43,789,157 (GRCm39) |
missense |
probably benign |
|
R4715:Abcc2
|
UTSW |
19 |
43,805,321 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4726:Abcc2
|
UTSW |
19 |
43,820,553 (GRCm39) |
missense |
probably benign |
0.23 |
R4760:Abcc2
|
UTSW |
19 |
43,798,920 (GRCm39) |
missense |
probably benign |
0.03 |
R4801:Abcc2
|
UTSW |
19 |
43,807,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Abcc2
|
UTSW |
19 |
43,807,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R4976:Abcc2
|
UTSW |
19 |
43,789,074 (GRCm39) |
missense |
probably benign |
0.34 |
R5143:Abcc2
|
UTSW |
19 |
43,810,100 (GRCm39) |
missense |
probably benign |
0.28 |
R5206:Abcc2
|
UTSW |
19 |
43,806,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R5376:Abcc2
|
UTSW |
19 |
43,818,339 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5478:Abcc2
|
UTSW |
19 |
43,827,904 (GRCm39) |
utr 3 prime |
probably benign |
|
R5700:Abcc2
|
UTSW |
19 |
43,786,633 (GRCm39) |
missense |
probably benign |
0.22 |
R5863:Abcc2
|
UTSW |
19 |
43,786,575 (GRCm39) |
missense |
probably benign |
0.00 |
R5928:Abcc2
|
UTSW |
19 |
43,807,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R5955:Abcc2
|
UTSW |
19 |
43,801,629 (GRCm39) |
missense |
probably damaging |
0.98 |
R5983:Abcc2
|
UTSW |
19 |
43,807,942 (GRCm39) |
missense |
probably benign |
|
R6014:Abcc2
|
UTSW |
19 |
43,815,174 (GRCm39) |
missense |
probably benign |
|
R6419:Abcc2
|
UTSW |
19 |
43,825,947 (GRCm39) |
splice site |
probably null |
|
R6497:Abcc2
|
UTSW |
19 |
43,793,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R6510:Abcc2
|
UTSW |
19 |
43,770,645 (GRCm39) |
splice site |
probably null |
|
R6614:Abcc2
|
UTSW |
19 |
43,807,800 (GRCm39) |
missense |
probably benign |
0.01 |
R6649:Abcc2
|
UTSW |
19 |
43,800,941 (GRCm39) |
missense |
probably benign |
0.05 |
R6653:Abcc2
|
UTSW |
19 |
43,800,941 (GRCm39) |
missense |
probably benign |
0.05 |
R6670:Abcc2
|
UTSW |
19 |
43,827,850 (GRCm39) |
utr 3 prime |
probably benign |
|
R6964:Abcc2
|
UTSW |
19 |
43,786,515 (GRCm39) |
missense |
probably benign |
0.12 |
R6989:Abcc2
|
UTSW |
19 |
43,820,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7015:Abcc2
|
UTSW |
19 |
43,786,617 (GRCm39) |
missense |
probably benign |
0.03 |
R7026:Abcc2
|
UTSW |
19 |
43,818,974 (GRCm39) |
missense |
probably benign |
0.01 |
R7026:Abcc2
|
UTSW |
19 |
43,805,392 (GRCm39) |
missense |
probably benign |
0.00 |
R7136:Abcc2
|
UTSW |
19 |
43,825,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R7252:Abcc2
|
UTSW |
19 |
43,816,388 (GRCm39) |
missense |
probably damaging |
0.98 |
R7293:Abcc2
|
UTSW |
19 |
43,795,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R7392:Abcc2
|
UTSW |
19 |
43,797,126 (GRCm39) |
missense |
probably damaging |
0.97 |
R7450:Abcc2
|
UTSW |
19 |
43,810,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R7654:Abcc2
|
UTSW |
19 |
43,815,032 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7787:Abcc2
|
UTSW |
19 |
43,772,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R7815:Abcc2
|
UTSW |
19 |
43,818,866 (GRCm39) |
missense |
probably benign |
0.01 |
R7911:Abcc2
|
UTSW |
19 |
43,792,109 (GRCm39) |
missense |
probably benign |
0.00 |
R7919:Abcc2
|
UTSW |
19 |
43,805,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R7925:Abcc2
|
UTSW |
19 |
43,795,551 (GRCm39) |
missense |
probably benign |
0.07 |
R7993:Abcc2
|
UTSW |
19 |
43,803,231 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8097:Abcc2
|
UTSW |
19 |
43,805,394 (GRCm39) |
missense |
probably benign |
0.10 |
R8177:Abcc2
|
UTSW |
19 |
43,795,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Abcc2
|
UTSW |
19 |
43,793,410 (GRCm39) |
missense |
probably benign |
0.07 |
R8693:Abcc2
|
UTSW |
19 |
43,810,474 (GRCm39) |
missense |
probably benign |
0.06 |
R8722:Abcc2
|
UTSW |
19 |
43,825,052 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8734:Abcc2
|
UTSW |
19 |
43,770,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Abcc2
|
UTSW |
19 |
43,787,577 (GRCm39) |
missense |
probably damaging |
0.99 |
R8774-TAIL:Abcc2
|
UTSW |
19 |
43,787,577 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:Abcc2
|
UTSW |
19 |
43,797,105 (GRCm39) |
missense |
probably benign |
0.01 |
R8889:Abcc2
|
UTSW |
19 |
43,795,571 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8892:Abcc2
|
UTSW |
19 |
43,795,571 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8936:Abcc2
|
UTSW |
19 |
43,797,101 (GRCm39) |
missense |
probably benign |
0.35 |
R9031:Abcc2
|
UTSW |
19 |
43,810,466 (GRCm39) |
missense |
probably benign |
|
R9116:Abcc2
|
UTSW |
19 |
43,793,391 (GRCm39) |
missense |
probably benign |
0.30 |
R9201:Abcc2
|
UTSW |
19 |
43,786,880 (GRCm39) |
missense |
probably damaging |
0.97 |
R9246:Abcc2
|
UTSW |
19 |
43,786,882 (GRCm39) |
missense |
probably benign |
0.01 |
R9345:Abcc2
|
UTSW |
19 |
43,807,869 (GRCm39) |
missense |
probably damaging |
0.97 |
R9487:Abcc2
|
UTSW |
19 |
43,806,471 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Abcc2
|
UTSW |
19 |
43,820,644 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Abcc2
|
UTSW |
19 |
43,811,539 (GRCm39) |
nonsense |
probably null |
|
Z1177:Abcc2
|
UTSW |
19 |
43,792,175 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Abcc2
|
UTSW |
19 |
43,792,173 (GRCm39) |
missense |
probably benign |
0.05 |
|