Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arfgef3 |
A |
G |
10: 18,528,280 (GRCm39) |
|
probably null |
Het |
Arid1a |
T |
C |
4: 133,479,973 (GRCm39) |
Y317C |
probably damaging |
Het |
Asxl2 |
A |
G |
12: 3,552,220 (GRCm39) |
T1321A |
probably benign |
Het |
Bckdk |
A |
G |
7: 127,504,931 (GRCm39) |
Y129C |
probably damaging |
Het |
Birc2 |
A |
G |
9: 7,834,301 (GRCm39) |
V60A |
probably benign |
Het |
Bmp8a |
T |
C |
4: 123,218,952 (GRCm39) |
H152R |
probably benign |
Het |
C3 |
T |
C |
17: 57,528,029 (GRCm39) |
H730R |
probably benign |
Het |
Ccser1 |
T |
A |
6: 61,289,088 (GRCm39) |
V417E |
probably benign |
Het |
Cfap58 |
T |
A |
19: 48,017,540 (GRCm39) |
M800K |
probably damaging |
Het |
Clip1 |
A |
G |
5: 123,780,627 (GRCm39) |
L352P |
probably damaging |
Het |
Cr2 |
A |
G |
1: 194,840,376 (GRCm39) |
L522P |
probably damaging |
Het |
Ctcf |
T |
A |
8: 106,393,379 (GRCm39) |
H347Q |
possibly damaging |
Het |
Gm13271 |
A |
T |
4: 88,673,318 (GRCm39) |
M72L |
probably benign |
Het |
Gpat4 |
GTGTT |
GT |
8: 23,669,498 (GRCm39) |
|
probably benign |
Het |
Ighv5-8 |
C |
T |
12: 113,618,813 (GRCm39) |
A76V |
unknown |
Het |
Irx5 |
G |
A |
8: 93,086,962 (GRCm39) |
G298D |
probably benign |
Het |
Klf5 |
T |
C |
14: 99,539,670 (GRCm39) |
I361T |
possibly damaging |
Het |
Lsm11 |
G |
A |
11: 45,835,591 (GRCm39) |
A50V |
probably benign |
Het |
Muc5b |
A |
T |
7: 141,405,552 (GRCm39) |
T954S |
unknown |
Het |
Nhsl1 |
A |
G |
10: 18,400,910 (GRCm39) |
N678S |
probably benign |
Het |
Npsr1 |
T |
A |
9: 24,221,377 (GRCm39) |
I277N |
possibly damaging |
Het |
Ntsr2 |
A |
G |
12: 16,706,821 (GRCm39) |
H283R |
probably damaging |
Het |
Obscn |
A |
T |
11: 58,893,829 (GRCm39) |
I6746N |
probably benign |
Het |
Obsl1 |
T |
C |
1: 75,480,350 (GRCm39) |
T425A |
probably benign |
Het |
Pag1 |
T |
A |
3: 9,759,112 (GRCm39) |
E335D |
probably benign |
Het |
Parp3 |
T |
A |
9: 106,351,447 (GRCm39) |
Q223L |
probably benign |
Het |
Pogz |
T |
C |
3: 94,786,061 (GRCm39) |
V883A |
probably benign |
Het |
Rsbn1l |
A |
T |
5: 21,132,665 (GRCm39) |
M198K |
probably benign |
Het |
Sh3bgr |
A |
G |
16: 96,007,680 (GRCm39) |
|
probably null |
Het |
Shc4 |
A |
G |
2: 125,471,617 (GRCm39) |
I600T |
probably damaging |
Het |
Slc26a1 |
T |
C |
5: 108,821,715 (GRCm39) |
H74R |
probably benign |
Het |
Slc7a11 |
A |
C |
3: 50,338,578 (GRCm39) |
I277S |
possibly damaging |
Het |
Tep1 |
G |
T |
14: 51,074,529 (GRCm39) |
T1832N |
probably benign |
Het |
Terf2 |
A |
G |
8: 107,809,613 (GRCm39) |
|
probably null |
Het |
Tle4 |
G |
A |
19: 14,432,323 (GRCm39) |
Q458* |
probably null |
Het |
Trim34b |
A |
T |
7: 103,979,083 (GRCm39) |
D110V |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,308,034 (GRCm39) |
N2267K |
possibly damaging |
Het |
Vmn2r50 |
G |
A |
7: 9,781,639 (GRCm39) |
Q369* |
probably null |
Het |
Zfp217 |
G |
A |
2: 169,961,571 (GRCm39) |
S252F |
possibly damaging |
Het |
Zfp229 |
T |
C |
17: 21,965,077 (GRCm39) |
S436P |
probably damaging |
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 |
|
R1770:Map1b
|
UTSW |
13 |
99,567,001 (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 |
|
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 |
|