Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd4 |
T |
C |
12: 84,661,874 (GRCm39) |
T84A |
probably benign |
Het |
Adgra1 |
T |
A |
7: 139,453,947 (GRCm39) |
Y161* |
probably null |
Het |
Aldoart1 |
G |
T |
4: 72,770,173 (GRCm39) |
H212N |
probably benign |
Het |
Aldob |
A |
G |
4: 49,536,861 (GRCm39) |
Y343H |
probably damaging |
Het |
Ankrd17 |
A |
T |
5: 90,391,235 (GRCm39) |
V2036E |
possibly damaging |
Het |
Ass1 |
A |
G |
2: 31,376,528 (GRCm39) |
T131A |
probably benign |
Het |
Baz1a |
C |
T |
12: 54,945,293 (GRCm39) |
R1354H |
probably damaging |
Het |
C2cd2l |
A |
G |
9: 44,228,108 (GRCm39) |
V71A |
probably benign |
Het |
C4b |
T |
A |
17: 34,955,901 (GRCm39) |
N678I |
possibly damaging |
Het |
Carmil1 |
A |
G |
13: 24,357,657 (GRCm39) |
L64P |
probably damaging |
Het |
Cdh18 |
T |
C |
15: 23,474,487 (GRCm39) |
S786P |
probably benign |
Het |
Cep135 |
A |
G |
5: 76,751,042 (GRCm39) |
E296G |
possibly damaging |
Het |
Chml |
G |
A |
1: 175,515,444 (GRCm39) |
T159I |
probably benign |
Het |
Cntn3 |
C |
T |
6: 102,246,166 (GRCm39) |
E328K |
possibly damaging |
Het |
Cstf1 |
A |
G |
2: 172,214,983 (GRCm39) |
I35V |
possibly damaging |
Het |
Cyp2c65 |
A |
G |
19: 39,070,642 (GRCm39) |
K275R |
probably benign |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dbx2 |
T |
C |
15: 95,522,615 (GRCm39) |
E364G |
probably benign |
Het |
Dcaf13 |
A |
T |
15: 38,993,633 (GRCm39) |
N242I |
probably damaging |
Het |
Dcc |
A |
G |
18: 71,579,470 (GRCm39) |
V701A |
probably benign |
Het |
Elapor2 |
A |
T |
5: 9,468,021 (GRCm39) |
T230S |
probably benign |
Het |
Fastkd5 |
A |
T |
2: 130,456,200 (GRCm39) |
Y797N |
probably damaging |
Het |
Fat4 |
T |
A |
3: 39,064,417 (GRCm39) |
I4791K |
probably damaging |
Het |
Gm3852 |
T |
C |
1: 46,051,048 (GRCm39) |
I45V |
possibly damaging |
Het |
Gng4 |
A |
G |
13: 13,999,851 (GRCm39) |
D40G |
probably damaging |
Het |
Gns |
A |
G |
10: 121,213,952 (GRCm39) |
D209G |
probably benign |
Het |
Kif6 |
C |
A |
17: 50,210,677 (GRCm39) |
Q791K |
possibly damaging |
Het |
Klhl35 |
G |
A |
7: 99,123,082 (GRCm39) |
V569M |
possibly damaging |
Het |
Krt1c |
A |
G |
15: 101,719,589 (GRCm39) |
S694P |
unknown |
Het |
Lrrc8c |
A |
G |
5: 105,754,603 (GRCm39) |
Y126C |
probably damaging |
Het |
Mad2l1bp |
A |
G |
17: 46,463,838 (GRCm39) |
V62A |
probably benign |
Het |
Mertk |
A |
G |
2: 128,592,094 (GRCm39) |
I273V |
probably benign |
Het |
Mfsd4b1 |
A |
G |
10: 39,879,223 (GRCm39) |
Y225H |
probably damaging |
Het |
Mrc2 |
T |
C |
11: 105,229,619 (GRCm39) |
V684A |
probably damaging |
Het |
Msh6 |
G |
A |
17: 88,287,651 (GRCm39) |
W97* |
probably null |
Het |
Mtmr10 |
A |
G |
7: 63,986,469 (GRCm39) |
I516V |
possibly damaging |
Het |
Myo7a |
A |
T |
7: 97,761,813 (GRCm39) |
|
probably benign |
Het |
Ndufs5 |
T |
C |
4: 123,606,661 (GRCm39) |
Y92C |
probably benign |
Het |
Nlrp1b |
C |
T |
11: 71,050,979 (GRCm39) |
V1035I |
probably benign |
Het |
Ntrk2 |
A |
G |
13: 59,009,132 (GRCm39) |
R308G |
possibly damaging |
Het |
Or12e13 |
A |
G |
2: 87,663,643 (GRCm39) |
I87V |
probably benign |
Het |
Pcdhb16 |
G |
T |
18: 37,612,233 (GRCm39) |
G398W |
probably damaging |
Het |
Plpbp |
T |
A |
8: 27,543,326 (GRCm39) |
S237T |
probably damaging |
Het |
Pnpla6 |
T |
A |
8: 3,584,634 (GRCm39) |
F769I |
possibly damaging |
Het |
Polk |
A |
G |
13: 96,631,950 (GRCm39) |
V261A |
probably damaging |
Het |
Prss52 |
C |
T |
14: 64,351,082 (GRCm39) |
A289V |
probably damaging |
Het |
Puf60 |
T |
C |
15: 75,942,723 (GRCm39) |
K407E |
probably benign |
Het |
Pzp |
T |
C |
6: 128,462,580 (GRCm39) |
D1455G |
probably damaging |
Het |
Ranbp17 |
T |
C |
11: 33,167,301 (GRCm39) |
N1054S |
probably benign |
Het |
Sdk2 |
A |
G |
11: 113,684,567 (GRCm39) |
S1965P |
probably benign |
Het |
Spryd7 |
T |
C |
14: 61,777,654 (GRCm39) |
Y142C |
probably damaging |
Het |
Srrt |
A |
T |
5: 137,298,122 (GRCm39) |
|
probably benign |
Het |
Stk10 |
A |
G |
11: 32,572,464 (GRCm39) |
E935G |
possibly damaging |
Het |
Tas2r115 |
G |
A |
6: 132,714,934 (GRCm39) |
R6C |
probably damaging |
Het |
Tdrd7 |
T |
A |
4: 45,987,681 (GRCm39) |
|
probably benign |
Het |
Trim29 |
A |
T |
9: 43,243,673 (GRCm39) |
Q564L |
probably damaging |
Het |
Trim5 |
T |
C |
7: 103,925,868 (GRCm39) |
D231G |
probably damaging |
Het |
Trpv2 |
A |
G |
11: 62,487,787 (GRCm39) |
K676E |
probably benign |
Het |
Ttn |
T |
C |
2: 76,583,859 (GRCm39) |
R22383G |
probably damaging |
Het |
Ugt1a2 |
A |
G |
1: 88,129,160 (GRCm39) |
I268V |
probably benign |
Het |
Ugt8a |
T |
C |
3: 125,667,852 (GRCm39) |
N330D |
probably benign |
Het |
Utrn |
G |
A |
10: 12,351,040 (GRCm39) |
H2822Y |
probably damaging |
Het |
Vmn1r176 |
G |
A |
7: 23,534,946 (GRCm39) |
A69V |
probably benign |
Het |
Vmn2r106 |
T |
C |
17: 20,488,560 (GRCm39) |
Y613C |
probably damaging |
Het |
Wdfy1 |
A |
T |
1: 79,686,857 (GRCm39) |
W296R |
probably damaging |
Het |
Zfp11 |
G |
A |
5: 129,734,822 (GRCm39) |
T213I |
possibly damaging |
Het |
Zfp142 |
A |
T |
1: 74,618,790 (GRCm39) |
F193I |
probably damaging |
Het |
Zfp764 |
G |
A |
7: 127,004,739 (GRCm39) |
Q131* |
probably null |
Het |
|
Other mutations in Map1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00508:Map1b
|
APN |
13 |
99,565,741 (GRCm39) |
missense |
unknown |
|
IGL00533:Map1b
|
APN |
13 |
99,569,112 (GRCm39) |
missense |
unknown |
|
IGL00801:Map1b
|
APN |
13 |
99,566,605 (GRCm39) |
missense |
unknown |
|
IGL01141:Map1b
|
APN |
13 |
99,571,269 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01418:Map1b
|
APN |
13 |
99,568,338 (GRCm39) |
missense |
unknown |
|
IGL01464:Map1b
|
APN |
13 |
99,569,251 (GRCm39) |
missense |
unknown |
|
IGL01690:Map1b
|
APN |
13 |
99,571,512 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01991:Map1b
|
APN |
13 |
99,566,077 (GRCm39) |
missense |
unknown |
|
IGL02245:Map1b
|
APN |
13 |
99,568,036 (GRCm39) |
missense |
unknown |
|
IGL02376:Map1b
|
APN |
13 |
99,572,103 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02380:Map1b
|
APN |
13 |
99,567,651 (GRCm39) |
missense |
unknown |
|
IGL02442:Map1b
|
APN |
13 |
99,644,706 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02465:Map1b
|
APN |
13 |
99,569,914 (GRCm39) |
missense |
unknown |
|
IGL02816:Map1b
|
APN |
13 |
99,578,263 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02859:Map1b
|
APN |
13 |
99,569,544 (GRCm39) |
missense |
unknown |
|
IGL02934:Map1b
|
APN |
13 |
99,571,639 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02970:Map1b
|
APN |
13 |
99,567,242 (GRCm39) |
nonsense |
probably null |
|
IGL03148:Map1b
|
APN |
13 |
99,578,203 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03401:Map1b
|
APN |
13 |
99,563,776 (GRCm39) |
missense |
unknown |
|
IGL03138:Map1b
|
UTSW |
13 |
99,562,334 (GRCm39) |
missense |
unknown |
|
R0006:Map1b
|
UTSW |
13 |
99,571,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Map1b
|
UTSW |
13 |
99,571,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R0035:Map1b
|
UTSW |
13 |
99,571,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R0069:Map1b
|
UTSW |
13 |
99,566,356 (GRCm39) |
missense |
unknown |
|
R0315:Map1b
|
UTSW |
13 |
99,567,624 (GRCm39) |
missense |
unknown |
|
R0539:Map1b
|
UTSW |
13 |
99,570,526 (GRCm39) |
missense |
unknown |
|
R0548:Map1b
|
UTSW |
13 |
99,568,191 (GRCm39) |
missense |
unknown |
|
R0613:Map1b
|
UTSW |
13 |
99,578,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Map1b
|
UTSW |
13 |
99,566,274 (GRCm39) |
nonsense |
probably null |
|
R1103:Map1b
|
UTSW |
13 |
99,563,974 (GRCm39) |
splice site |
probably benign |
|
R1300:Map1b
|
UTSW |
13 |
99,569,029 (GRCm39) |
missense |
unknown |
|
R1353:Map1b
|
UTSW |
13 |
99,563,834 (GRCm39) |
missense |
unknown |
|
R1387:Map1b
|
UTSW |
13 |
99,569,158 (GRCm39) |
missense |
unknown |
|
R1481:Map1b
|
UTSW |
13 |
99,567,679 (GRCm39) |
missense |
unknown |
|
R1509:Map1b
|
UTSW |
13 |
99,568,036 (GRCm39) |
missense |
unknown |
|
R1521:Map1b
|
UTSW |
13 |
99,569,247 (GRCm39) |
missense |
unknown |
|
R1604:Map1b
|
UTSW |
13 |
99,566,080 (GRCm39) |
missense |
unknown |
|
R1649:Map1b
|
UTSW |
13 |
99,652,986 (GRCm39) |
missense |
probably benign |
0.03 |
R1651:Map1b
|
UTSW |
13 |
99,569,091 (GRCm39) |
missense |
unknown |
|
R1661:Map1b
|
UTSW |
13 |
99,568,437 (GRCm39) |
missense |
unknown |
|
R1665:Map1b
|
UTSW |
13 |
99,568,437 (GRCm39) |
missense |
unknown |
|
R1926:Map1b
|
UTSW |
13 |
99,567,200 (GRCm39) |
missense |
unknown |
|
R1928:Map1b
|
UTSW |
13 |
99,567,454 (GRCm39) |
missense |
unknown |
|
R2093:Map1b
|
UTSW |
13 |
99,566,178 (GRCm39) |
missense |
unknown |
|
R2110:Map1b
|
UTSW |
13 |
99,567,629 (GRCm39) |
missense |
unknown |
|
R2116:Map1b
|
UTSW |
13 |
99,567,152 (GRCm39) |
missense |
unknown |
|
R2164:Map1b
|
UTSW |
13 |
99,565,846 (GRCm39) |
missense |
unknown |
|
R2207:Map1b
|
UTSW |
13 |
99,567,591 (GRCm39) |
missense |
unknown |
|
R2273:Map1b
|
UTSW |
13 |
99,568,592 (GRCm39) |
missense |
unknown |
|
R2443:Map1b
|
UTSW |
13 |
99,566,919 (GRCm39) |
missense |
unknown |
|
R3054:Map1b
|
UTSW |
13 |
99,569,250 (GRCm39) |
missense |
unknown |
|
R3766:Map1b
|
UTSW |
13 |
99,570,595 (GRCm39) |
missense |
unknown |
|
R3911:Map1b
|
UTSW |
13 |
99,567,580 (GRCm39) |
missense |
unknown |
|
R4005:Map1b
|
UTSW |
13 |
99,566,415 (GRCm39) |
missense |
unknown |
|
R4130:Map1b
|
UTSW |
13 |
99,568,188 (GRCm39) |
missense |
unknown |
|
R4513:Map1b
|
UTSW |
13 |
99,580,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Map1b
|
UTSW |
13 |
99,566,810 (GRCm39) |
nonsense |
probably null |
|
R4633:Map1b
|
UTSW |
13 |
99,571,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R4646:Map1b
|
UTSW |
13 |
99,568,977 (GRCm39) |
missense |
unknown |
|
R4690:Map1b
|
UTSW |
13 |
99,567,576 (GRCm39) |
missense |
unknown |
|
R4704:Map1b
|
UTSW |
13 |
99,566,983 (GRCm39) |
missense |
unknown |
|
R4836:Map1b
|
UTSW |
13 |
99,567,562 (GRCm39) |
missense |
unknown |
|
R4916:Map1b
|
UTSW |
13 |
99,569,808 (GRCm39) |
missense |
unknown |
|
R4951:Map1b
|
UTSW |
13 |
99,568,935 (GRCm39) |
missense |
unknown |
|
R4960:Map1b
|
UTSW |
13 |
99,568,720 (GRCm39) |
missense |
probably benign |
0.23 |
R4961:Map1b
|
UTSW |
13 |
99,572,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R5030:Map1b
|
UTSW |
13 |
99,570,682 (GRCm39) |
missense |
unknown |
|
R5090:Map1b
|
UTSW |
13 |
99,566,534 (GRCm39) |
nonsense |
probably null |
|
R5469:Map1b
|
UTSW |
13 |
99,565,846 (GRCm39) |
missense |
unknown |
|
R5820:Map1b
|
UTSW |
13 |
99,569,332 (GRCm39) |
missense |
unknown |
|
R5885:Map1b
|
UTSW |
13 |
99,566,589 (GRCm39) |
missense |
unknown |
|
R5915:Map1b
|
UTSW |
13 |
99,566,839 (GRCm39) |
missense |
unknown |
|
R5923:Map1b
|
UTSW |
13 |
99,569,661 (GRCm39) |
missense |
unknown |
|
R6063:Map1b
|
UTSW |
13 |
99,567,645 (GRCm39) |
missense |
unknown |
|
R6102:Map1b
|
UTSW |
13 |
99,562,381 (GRCm39) |
missense |
unknown |
|
R6218:Map1b
|
UTSW |
13 |
99,569,714 (GRCm39) |
missense |
unknown |
|
R6435:Map1b
|
UTSW |
13 |
99,652,871 (GRCm39) |
missense |
probably damaging |
0.99 |
R6663:Map1b
|
UTSW |
13 |
99,566,530 (GRCm39) |
missense |
unknown |
|
R6765:Map1b
|
UTSW |
13 |
99,562,449 (GRCm39) |
missense |
unknown |
|
R6860:Map1b
|
UTSW |
13 |
99,571,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R6997:Map1b
|
UTSW |
13 |
99,567,142 (GRCm39) |
missense |
unknown |
|
R7001:Map1b
|
UTSW |
13 |
99,567,101 (GRCm39) |
missense |
unknown |
|
R7310:Map1b
|
UTSW |
13 |
99,570,163 (GRCm39) |
missense |
unknown |
|
R7349:Map1b
|
UTSW |
13 |
99,570,148 (GRCm39) |
missense |
unknown |
|
R7448:Map1b
|
UTSW |
13 |
99,644,648 (GRCm39) |
missense |
probably damaging |
0.99 |
R7449:Map1b
|
UTSW |
13 |
99,644,648 (GRCm39) |
missense |
probably damaging |
0.99 |
R7452:Map1b
|
UTSW |
13 |
99,644,648 (GRCm39) |
missense |
probably damaging |
0.99 |
R7810:Map1b
|
UTSW |
13 |
99,568,390 (GRCm39) |
missense |
unknown |
|
R7820:Map1b
|
UTSW |
13 |
99,567,685 (GRCm39) |
missense |
unknown |
|
R8396:Map1b
|
UTSW |
13 |
99,570,621 (GRCm39) |
missense |
unknown |
|
R8470:Map1b
|
UTSW |
13 |
99,652,950 (GRCm39) |
missense |
probably damaging |
0.98 |
R8535:Map1b
|
UTSW |
13 |
99,571,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R8777:Map1b
|
UTSW |
13 |
99,567,304 (GRCm39) |
missense |
unknown |
|
R8777-TAIL:Map1b
|
UTSW |
13 |
99,567,304 (GRCm39) |
missense |
unknown |
|
R8812:Map1b
|
UTSW |
13 |
99,569,323 (GRCm39) |
missense |
unknown |
|
R8903:Map1b
|
UTSW |
13 |
99,569,017 (GRCm39) |
nonsense |
probably null |
|
R8928:Map1b
|
UTSW |
13 |
99,568,624 (GRCm39) |
missense |
unknown |
|
R8954:Map1b
|
UTSW |
13 |
99,570,735 (GRCm39) |
missense |
unknown |
|
R9164:Map1b
|
UTSW |
13 |
99,568,816 (GRCm39) |
nonsense |
probably null |
|
R9164:Map1b
|
UTSW |
13 |
99,562,351 (GRCm39) |
missense |
unknown |
|
R9190:Map1b
|
UTSW |
13 |
99,571,914 (GRCm39) |
missense |
probably damaging |
0.99 |
R9334:Map1b
|
UTSW |
13 |
99,568,148 (GRCm39) |
missense |
unknown |
|
R9339:Map1b
|
UTSW |
13 |
99,567,570 (GRCm39) |
missense |
unknown |
|
R9357:Map1b
|
UTSW |
13 |
99,566,708 (GRCm39) |
nonsense |
probably null |
|
R9430:Map1b
|
UTSW |
13 |
99,570,616 (GRCm39) |
missense |
unknown |
|
RF003:Map1b
|
UTSW |
13 |
99,567,258 (GRCm39) |
missense |
unknown |
|
X0019:Map1b
|
UTSW |
13 |
99,568,920 (GRCm39) |
missense |
unknown |
|
X0019:Map1b
|
UTSW |
13 |
99,566,476 (GRCm39) |
missense |
unknown |
|
Z1088:Map1b
|
UTSW |
13 |
99,644,623 (GRCm39) |
missense |
probably benign |
0.07 |
|