Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm3 |
T |
A |
7: 119,379,978 (GRCm39) |
|
probably null |
Het |
AW551984 |
T |
C |
9: 39,504,292 (GRCm39) |
D558G |
probably damaging |
Het |
Bcl9l |
GTGAACATGAACATGAACATGAAC |
GTGAACATGAACATGAACATGAACATGAAC |
9: 44,418,369 (GRCm39) |
|
probably benign |
Het |
Brd8dc |
A |
G |
18: 34,719,319 (GRCm39) |
V167A |
possibly damaging |
Het |
Ccdc12 |
T |
G |
9: 110,537,595 (GRCm39) |
|
probably null |
Het |
Ctsl |
T |
C |
13: 64,511,916 (GRCm39) |
|
probably null |
Het |
Cul1 |
T |
A |
6: 47,494,068 (GRCm39) |
D460E |
probably damaging |
Het |
Dnttip2 |
T |
A |
3: 122,069,870 (GRCm39) |
S362T |
probably damaging |
Het |
Fbxw16 |
T |
A |
9: 109,267,280 (GRCm39) |
D317V |
probably damaging |
Het |
Fbxw9 |
T |
A |
8: 85,788,839 (GRCm39) |
N196K |
possibly damaging |
Het |
Grap |
A |
G |
11: 61,551,064 (GRCm39) |
D32G |
probably damaging |
Het |
Hhatl |
T |
C |
9: 121,618,137 (GRCm39) |
D206G |
probably damaging |
Het |
Hrnr |
A |
T |
3: 93,239,192 (GRCm39) |
Q3143H |
unknown |
Het |
Ighv1-62-1 |
T |
C |
12: 115,350,529 (GRCm39) |
Y46C |
probably damaging |
Het |
Krtap16-3 |
A |
T |
16: 88,759,540 (GRCm39) |
Y58N |
unknown |
Het |
Mef2c |
A |
G |
13: 83,810,716 (GRCm39) |
K384R |
probably damaging |
Het |
Nalcn |
A |
G |
14: 123,702,084 (GRCm39) |
Y476H |
possibly damaging |
Het |
Oxgr1 |
A |
T |
14: 120,259,669 (GRCm39) |
N179K |
probably damaging |
Het |
Polk |
G |
A |
13: 96,633,138 (GRCm39) |
Q302* |
probably null |
Het |
Rab3gap1 |
T |
A |
1: 127,858,512 (GRCm39) |
S540R |
probably benign |
Het |
Samd5 |
A |
T |
10: 9,504,808 (GRCm39) |
|
probably null |
Het |
Sema6d |
GTGATAC |
G |
2: 124,496,762 (GRCm39) |
|
probably benign |
Het |
Slc1a6 |
C |
A |
10: 78,623,646 (GRCm39) |
A15D |
probably benign |
Het |
Slc8a1 |
A |
G |
17: 81,956,883 (GRCm39) |
C52R |
probably damaging |
Het |
Sod2 |
T |
A |
17: 13,227,252 (GRCm39) |
Y69N |
possibly damaging |
Het |
Tank |
T |
C |
2: 61,474,768 (GRCm39) |
|
probably null |
Het |
Tbc1d23 |
A |
T |
16: 57,034,580 (GRCm39) |
I73N |
probably benign |
Het |
Tnf |
A |
C |
17: 35,420,800 (GRCm39) |
M6R |
possibly damaging |
Het |
Trmt2a |
C |
T |
16: 18,068,341 (GRCm39) |
A16V |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,556,055 (GRCm39) |
Y21990H |
probably damaging |
Het |
Uaca |
C |
T |
9: 60,779,306 (GRCm39) |
S1231L |
probably benign |
Het |
Ubr1 |
A |
G |
2: 120,754,611 (GRCm39) |
|
probably null |
Het |
Unc13b |
A |
G |
4: 43,255,562 (GRCm39) |
D3849G |
probably damaging |
Het |
Vmn2r75 |
T |
A |
7: 85,797,644 (GRCm39) |
D723V |
probably damaging |
Het |
Wnt2 |
C |
A |
6: 18,028,091 (GRCm39) |
V48L |
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 |
R1606:Abcc2
|
UTSW |
19 |
43,825,091 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|