Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acacb |
A |
G |
5: 114,207,348 (GRCm38) |
D954G |
probably damaging |
Het |
Acvr1 |
T |
C |
2: 58,462,913 (GRCm38) |
K345R |
probably null |
Het |
Aldoart2 |
A |
G |
12: 55,566,319 (GRCm38) |
Y343C |
probably damaging |
Het |
Arpp21 |
T |
A |
9: 112,065,979 (GRCm38) |
Y739F |
possibly damaging |
Het |
Cachd1 |
C |
A |
4: 100,974,880 (GRCm38) |
Y746* |
probably null |
Het |
Card14 |
T |
C |
11: 119,333,932 (GRCm38) |
V595A |
probably damaging |
Het |
Dhx33 |
T |
C |
11: 70,989,152 (GRCm38) |
D344G |
probably benign |
Het |
Dnah12 |
T |
A |
14: 26,706,065 (GRCm38) |
D171E |
probably benign |
Het |
Fat3 |
A |
G |
9: 16,247,041 (GRCm38) |
|
probably benign |
Het |
Fmnl3 |
A |
G |
15: 99,321,864 (GRCm38) |
F668L |
probably damaging |
Het |
Frmpd4 |
G |
A |
X: 167,486,807 (GRCm38) |
T493M |
probably damaging |
Het |
Gcn1l1 |
A |
T |
5: 115,583,394 (GRCm38) |
|
probably benign |
Het |
Hspbp1 |
G |
T |
7: 4,677,809 (GRCm38) |
Q223K |
probably damaging |
Het |
Ighv1-19 |
C |
A |
12: 114,708,877 (GRCm38) |
C40F |
probably damaging |
Het |
Igkv4-90 |
A |
G |
6: 68,807,681 (GRCm38) |
F10L |
probably benign |
Het |
Kctd5 |
T |
C |
17: 24,059,238 (GRCm38) |
D146G |
probably benign |
Het |
Kif4-ps |
A |
G |
12: 101,146,110 (GRCm38) |
E166G |
probably damaging |
Het |
Lemd3 |
T |
C |
10: 120,928,015 (GRCm38) |
D780G |
probably damaging |
Het |
Manba |
G |
A |
3: 135,554,850 (GRCm38) |
V599I |
probably benign |
Het |
Map2 |
A |
G |
1: 66,412,446 (GRCm38) |
E247G |
possibly damaging |
Het |
Mfsd1 |
T |
C |
3: 67,582,965 (GRCm38) |
F50L |
probably benign |
Het |
Mier2 |
T |
C |
10: 79,545,042 (GRCm38) |
|
probably benign |
Het |
Nol10 |
A |
T |
12: 17,424,673 (GRCm38) |
K622I |
probably benign |
Het |
Olfr486 |
A |
T |
7: 108,172,309 (GRCm38) |
I145N |
probably benign |
Het |
Olfr926 |
T |
C |
9: 38,877,251 (GRCm38) |
F25S |
probably damaging |
Het |
Phtf1 |
A |
G |
3: 103,985,779 (GRCm38) |
M120V |
probably benign |
Het |
Prrx1 |
A |
G |
1: 163,261,877 (GRCm38) |
L127P |
probably damaging |
Het |
Rbsn |
T |
C |
6: 92,191,335 (GRCm38) |
M373V |
possibly damaging |
Het |
Sec24b |
T |
C |
3: 130,033,833 (GRCm38) |
K203R |
possibly damaging |
Het |
Shroom3 |
G |
T |
5: 92,943,086 (GRCm38) |
V1151F |
probably damaging |
Het |
Slc16a10 |
G |
C |
10: 40,056,624 (GRCm38) |
H314D |
possibly damaging |
Het |
Slc4a7 |
A |
T |
14: 14,729,276 (GRCm38) |
E47D |
probably damaging |
Het |
Taf12 |
C |
A |
4: 132,282,954 (GRCm38) |
P78Q |
probably damaging |
Het |
Tnn |
A |
G |
1: 160,146,240 (GRCm38) |
C186R |
probably damaging |
Het |
Trim46 |
T |
A |
3: 89,234,949 (GRCm38) |
T721S |
probably benign |
Het |
Trip4 |
T |
C |
9: 65,880,942 (GRCm38) |
N74D |
possibly damaging |
Het |
Tssk5 |
C |
T |
15: 76,372,896 (GRCm38) |
R262H |
probably benign |
Het |
Vegfa |
T |
C |
17: 46,024,520 (GRCm38) |
I105V |
possibly damaging |
Het |
Vmn2r14 |
T |
C |
5: 109,216,229 (GRCm38) |
Y607C |
probably damaging |
Het |
Wdr83 |
G |
T |
8: 85,080,339 (GRCm38) |
H66Q |
probably damaging |
Het |
Zfp280b |
A |
G |
10: 76,039,102 (GRCm38) |
T272A |
probably benign |
Het |
Zfp960 |
T |
A |
17: 17,088,371 (GRCm38) |
L449H |
probably damaging |
Het |
|
Other mutations in Mslnl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01621:Mslnl
|
APN |
17 |
25,743,667 (GRCm38) |
unclassified |
probably benign |
|
IGL01629:Mslnl
|
APN |
17 |
25,744,775 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL02084:Mslnl
|
APN |
17 |
25,746,151 (GRCm38) |
missense |
probably benign |
0.07 |
IGL02408:Mslnl
|
APN |
17 |
25,747,998 (GRCm38) |
missense |
possibly damaging |
0.80 |
IGL02726:Mslnl
|
APN |
17 |
25,744,103 (GRCm38) |
critical splice donor site |
probably null |
|
IGL03387:Mslnl
|
APN |
17 |
25,744,077 (GRCm38) |
missense |
probably benign |
0.06 |
R0561:Mslnl
|
UTSW |
17 |
25,743,203 (GRCm38) |
nonsense |
probably null |
|
R0881:Mslnl
|
UTSW |
17 |
25,742,965 (GRCm38) |
missense |
possibly damaging |
0.82 |
R1295:Mslnl
|
UTSW |
17 |
25,743,240 (GRCm38) |
missense |
probably damaging |
1.00 |
R1296:Mslnl
|
UTSW |
17 |
25,743,240 (GRCm38) |
missense |
probably damaging |
1.00 |
R1582:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R1629:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R1630:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R1631:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R1632:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R1794:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R1850:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R1866:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R1876:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R1914:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2166:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2241:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2243:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2247:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2282:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2284:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2852:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2867:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2867:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2877:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2878:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2919:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R2920:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R3026:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R3405:Mslnl
|
UTSW |
17 |
25,746,181 (GRCm38) |
missense |
probably damaging |
1.00 |
R3406:Mslnl
|
UTSW |
17 |
25,746,181 (GRCm38) |
missense |
probably damaging |
1.00 |
R3411:Mslnl
|
UTSW |
17 |
25,744,517 (GRCm38) |
missense |
probably benign |
0.05 |
R3434:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R3546:Mslnl
|
UTSW |
17 |
25,744,969 (GRCm38) |
missense |
probably damaging |
0.98 |
R3612:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R3730:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R3802:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R3804:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R3894:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R3895:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R4454:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R4455:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R4456:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R4457:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R4561:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R4562:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R4564:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R4600:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R4601:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R4610:Mslnl
|
UTSW |
17 |
25,742,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R4704:Mslnl
|
UTSW |
17 |
25,738,978 (GRCm38) |
missense |
possibly damaging |
0.73 |
R5155:Mslnl
|
UTSW |
17 |
25,738,968 (GRCm38) |
nonsense |
probably null |
|
R5257:Mslnl
|
UTSW |
17 |
25,746,165 (GRCm38) |
missense |
probably benign |
0.00 |
R5456:Mslnl
|
UTSW |
17 |
25,743,159 (GRCm38) |
missense |
probably damaging |
0.98 |
R5645:Mslnl
|
UTSW |
17 |
25,737,842 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6007:Mslnl
|
UTSW |
17 |
25,746,775 (GRCm38) |
missense |
probably benign |
0.00 |
R6083:Mslnl
|
UTSW |
17 |
25,737,902 (GRCm38) |
missense |
possibly damaging |
0.83 |
R6142:Mslnl
|
UTSW |
17 |
25,744,557 (GRCm38) |
missense |
probably damaging |
1.00 |
R6761:Mslnl
|
UTSW |
17 |
25,746,073 (GRCm38) |
missense |
probably damaging |
1.00 |
R7058:Mslnl
|
UTSW |
17 |
25,743,212 (GRCm38) |
missense |
probably benign |
0.03 |
R7156:Mslnl
|
UTSW |
17 |
25,743,210 (GRCm38) |
missense |
probably benign |
0.20 |
R7467:Mslnl
|
UTSW |
17 |
25,736,921 (GRCm38) |
start codon destroyed |
probably benign |
0.33 |
R7687:Mslnl
|
UTSW |
17 |
25,743,183 (GRCm38) |
missense |
probably damaging |
0.97 |
R7807:Mslnl
|
UTSW |
17 |
25,746,777 (GRCm38) |
missense |
probably benign |
0.03 |
R8682:Mslnl
|
UTSW |
17 |
25,746,988 (GRCm38) |
missense |
probably benign |
|
R8735:Mslnl
|
UTSW |
17 |
25,745,088 (GRCm38) |
missense |
probably benign |
0.09 |
R8742:Mslnl
|
UTSW |
17 |
25,745,073 (GRCm38) |
missense |
probably damaging |
1.00 |
R9208:Mslnl
|
UTSW |
17 |
25,742,720 (GRCm38) |
missense |
possibly damaging |
0.94 |
R9264:Mslnl
|
UTSW |
17 |
25,742,532 (GRCm38) |
intron |
probably benign |
|
RF007:Mslnl
|
UTSW |
17 |
25,743,228 (GRCm38) |
missense |
possibly damaging |
0.87 |
|