Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
C |
A |
1: 12,042,300 (GRCm39) |
S440* |
probably null |
Het |
Chrdl2 |
A |
G |
7: 99,671,229 (GRCm39) |
T116A |
probably damaging |
Het |
Chst12 |
T |
C |
5: 140,510,401 (GRCm39) |
F343L |
probably damaging |
Het |
Cpeb2 |
T |
A |
5: 43,392,578 (GRCm39) |
|
probably benign |
Het |
Cyp27b1 |
A |
G |
10: 126,886,957 (GRCm39) |
D391G |
probably benign |
Het |
Dll3 |
T |
C |
7: 28,001,082 (GRCm39) |
|
probably null |
Het |
Dnah7b |
T |
A |
1: 46,260,932 (GRCm39) |
I2030N |
probably damaging |
Het |
Fap |
C |
T |
2: 62,361,051 (GRCm39) |
|
probably null |
Het |
Frmd4a |
C |
T |
2: 4,337,889 (GRCm39) |
R32C |
probably benign |
Het |
Fzd7 |
T |
C |
1: 59,523,566 (GRCm39) |
V483A |
probably damaging |
Het |
Gpm6a |
T |
C |
8: 55,500,428 (GRCm39) |
|
probably null |
Het |
Gprc6a |
T |
C |
10: 51,492,735 (GRCm39) |
H539R |
probably damaging |
Het |
Irs1 |
C |
T |
1: 82,265,685 (GRCm39) |
A844T |
probably benign |
Het |
Myo1a |
T |
G |
10: 127,549,950 (GRCm39) |
S477A |
probably benign |
Het |
Naga |
C |
T |
15: 82,221,095 (GRCm39) |
W67* |
probably null |
Het |
Or51ah3 |
G |
C |
7: 103,210,380 (GRCm39) |
R232T |
possibly damaging |
Het |
Or51ah3 |
A |
T |
7: 103,210,379 (GRCm39) |
R232* |
probably null |
Het |
Osbpl1a |
T |
C |
18: 12,952,652 (GRCm39) |
E87G |
probably benign |
Het |
Prr27 |
A |
G |
5: 87,990,766 (GRCm39) |
H126R |
probably benign |
Het |
Rb1 |
G |
A |
14: 73,500,135 (GRCm39) |
T504I |
probably damaging |
Het |
Rnf144b |
A |
G |
13: 47,396,418 (GRCm39) |
N252D |
probably damaging |
Het |
Spaca7b |
T |
A |
8: 11,728,590 (GRCm39) |
N27I |
probably damaging |
Het |
Tas2r124 |
A |
G |
6: 132,731,954 (GRCm39) |
I88V |
probably benign |
Het |
Trip11 |
A |
G |
12: 101,853,198 (GRCm39) |
F465L |
probably benign |
Het |
Usp31 |
G |
A |
7: 121,306,152 (GRCm39) |
P109S |
possibly damaging |
Het |
Vmn2r12 |
A |
G |
5: 109,233,872 (GRCm39) |
L780P |
probably damaging |
Het |
Vmn2r71 |
G |
T |
7: 85,273,360 (GRCm39) |
D725Y |
probably damaging |
Het |
Zfp459 |
T |
C |
13: 67,561,307 (GRCm39) |
K47R |
probably damaging |
Het |
|
Other mutations in Slit2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00791:Slit2
|
APN |
5 |
48,461,374 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL00809:Slit2
|
APN |
5 |
48,146,493 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00811:Slit2
|
APN |
5 |
48,146,493 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00813:Slit2
|
APN |
5 |
48,146,493 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00815:Slit2
|
APN |
5 |
48,146,493 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00816:Slit2
|
APN |
5 |
48,146,493 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00817:Slit2
|
APN |
5 |
48,146,493 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00819:Slit2
|
APN |
5 |
48,146,493 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00820:Slit2
|
APN |
5 |
48,146,493 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00822:Slit2
|
APN |
5 |
48,146,493 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01077:Slit2
|
APN |
5 |
48,374,785 (GRCm39) |
splice site |
probably null |
|
IGL01375:Slit2
|
APN |
5 |
48,439,056 (GRCm39) |
splice site |
probably benign |
|
IGL01481:Slit2
|
APN |
5 |
48,460,273 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01934:Slit2
|
APN |
5 |
48,395,747 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01992:Slit2
|
APN |
5 |
48,395,759 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02315:Slit2
|
APN |
5 |
48,145,213 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02328:Slit2
|
APN |
5 |
48,387,646 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02366:Slit2
|
APN |
5 |
48,461,410 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02526:Slit2
|
APN |
5 |
48,461,565 (GRCm39) |
nonsense |
probably null |
|
IGL02852:Slit2
|
APN |
5 |
48,402,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02887:Slit2
|
APN |
5 |
48,374,816 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03123:Slit2
|
APN |
5 |
48,368,681 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03182:Slit2
|
APN |
5 |
48,377,395 (GRCm39) |
missense |
possibly damaging |
0.77 |
P0025:Slit2
|
UTSW |
5 |
48,461,377 (GRCm39) |
missense |
probably damaging |
0.96 |
R0032:Slit2
|
UTSW |
5 |
48,414,198 (GRCm39) |
missense |
probably damaging |
0.99 |
R0032:Slit2
|
UTSW |
5 |
48,414,198 (GRCm39) |
missense |
probably damaging |
0.99 |
R0055:Slit2
|
UTSW |
5 |
48,439,068 (GRCm39) |
nonsense |
probably null |
|
R0055:Slit2
|
UTSW |
5 |
48,439,068 (GRCm39) |
nonsense |
probably null |
|
R0267:Slit2
|
UTSW |
5 |
48,339,673 (GRCm39) |
splice site |
probably benign |
|
R0552:Slit2
|
UTSW |
5 |
48,395,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R0610:Slit2
|
UTSW |
5 |
48,433,016 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0883:Slit2
|
UTSW |
5 |
48,402,915 (GRCm39) |
splice site |
probably benign |
|
R1390:Slit2
|
UTSW |
5 |
48,374,832 (GRCm39) |
missense |
probably benign |
0.06 |
R1442:Slit2
|
UTSW |
5 |
48,395,725 (GRCm39) |
missense |
probably damaging |
0.96 |
R1453:Slit2
|
UTSW |
5 |
48,414,393 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1508:Slit2
|
UTSW |
5 |
48,349,591 (GRCm39) |
missense |
probably damaging |
0.98 |
R1639:Slit2
|
UTSW |
5 |
48,416,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R1705:Slit2
|
UTSW |
5 |
48,346,814 (GRCm39) |
missense |
probably damaging |
0.99 |
R1828:Slit2
|
UTSW |
5 |
48,461,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R1897:Slit2
|
UTSW |
5 |
48,395,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Slit2
|
UTSW |
5 |
48,439,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Slit2
|
UTSW |
5 |
48,348,358 (GRCm39) |
unclassified |
probably benign |
|
R1982:Slit2
|
UTSW |
5 |
48,407,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R2013:Slit2
|
UTSW |
5 |
48,459,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R2136:Slit2
|
UTSW |
5 |
48,461,567 (GRCm39) |
missense |
probably benign |
0.03 |
R2655:Slit2
|
UTSW |
5 |
48,346,917 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3402:Slit2
|
UTSW |
5 |
48,440,763 (GRCm39) |
missense |
probably damaging |
0.98 |
R3724:Slit2
|
UTSW |
5 |
48,414,225 (GRCm39) |
critical splice donor site |
probably null |
|
R4176:Slit2
|
UTSW |
5 |
48,394,586 (GRCm39) |
splice site |
probably null |
|
R4397:Slit2
|
UTSW |
5 |
48,377,423 (GRCm39) |
critical splice donor site |
probably null |
|
R4525:Slit2
|
UTSW |
5 |
48,407,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R4688:Slit2
|
UTSW |
5 |
48,414,345 (GRCm39) |
splice site |
probably null |
|
R5026:Slit2
|
UTSW |
5 |
48,414,147 (GRCm39) |
missense |
probably damaging |
0.99 |
R5138:Slit2
|
UTSW |
5 |
48,439,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R5465:Slit2
|
UTSW |
5 |
48,407,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R5471:Slit2
|
UTSW |
5 |
48,346,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R5699:Slit2
|
UTSW |
5 |
48,378,333 (GRCm39) |
critical splice donor site |
probably null |
|
R5735:Slit2
|
UTSW |
5 |
48,416,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R5834:Slit2
|
UTSW |
5 |
48,416,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R5967:Slit2
|
UTSW |
5 |
48,142,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R6150:Slit2
|
UTSW |
5 |
48,461,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6219:Slit2
|
UTSW |
5 |
48,459,770 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6344:Slit2
|
UTSW |
5 |
48,377,023 (GRCm39) |
missense |
probably benign |
0.07 |
R6408:Slit2
|
UTSW |
5 |
48,142,328 (GRCm39) |
unclassified |
probably benign |
|
R6479:Slit2
|
UTSW |
5 |
48,389,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R6526:Slit2
|
UTSW |
5 |
48,461,509 (GRCm39) |
missense |
probably damaging |
0.99 |
R6959:Slit2
|
UTSW |
5 |
48,395,727 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7139:Slit2
|
UTSW |
5 |
48,402,025 (GRCm39) |
missense |
probably benign |
0.19 |
R7201:Slit2
|
UTSW |
5 |
48,394,627 (GRCm39) |
missense |
probably null |
0.85 |
R7472:Slit2
|
UTSW |
5 |
48,414,180 (GRCm39) |
missense |
probably damaging |
0.97 |
R7491:Slit2
|
UTSW |
5 |
48,377,336 (GRCm39) |
missense |
probably benign |
0.18 |
R7566:Slit2
|
UTSW |
5 |
48,407,239 (GRCm39) |
missense |
probably damaging |
0.99 |
R7622:Slit2
|
UTSW |
5 |
48,142,547 (GRCm39) |
missense |
probably damaging |
0.98 |
R7831:Slit2
|
UTSW |
5 |
48,402,025 (GRCm39) |
missense |
probably benign |
0.19 |
R7870:Slit2
|
UTSW |
5 |
48,459,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R7899:Slit2
|
UTSW |
5 |
48,404,527 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7969:Slit2
|
UTSW |
5 |
48,461,378 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7984:Slit2
|
UTSW |
5 |
48,333,465 (GRCm39) |
intron |
probably benign |
|
R8021:Slit2
|
UTSW |
5 |
48,459,834 (GRCm39) |
nonsense |
probably null |
|
R8253:Slit2
|
UTSW |
5 |
48,433,013 (GRCm39) |
missense |
probably benign |
0.00 |
R8321:Slit2
|
UTSW |
5 |
48,387,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R8426:Slit2
|
UTSW |
5 |
48,382,105 (GRCm39) |
missense |
probably benign |
0.00 |
R8513:Slit2
|
UTSW |
5 |
48,382,050 (GRCm39) |
nonsense |
probably null |
|
R8756:Slit2
|
UTSW |
5 |
48,459,829 (GRCm39) |
nonsense |
probably null |
|
R8796:Slit2
|
UTSW |
5 |
48,460,190 (GRCm39) |
missense |
probably benign |
0.01 |
R8799:Slit2
|
UTSW |
5 |
48,461,524 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8947:Slit2
|
UTSW |
5 |
48,407,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R9005:Slit2
|
UTSW |
5 |
48,459,860 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9173:Slit2
|
UTSW |
5 |
48,377,285 (GRCm39) |
missense |
probably damaging |
0.98 |
R9310:Slit2
|
UTSW |
5 |
48,349,568 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9365:Slit2
|
UTSW |
5 |
48,461,534 (GRCm39) |
missense |
probably benign |
0.04 |
Z1088:Slit2
|
UTSW |
5 |
48,459,695 (GRCm39) |
missense |
probably damaging |
1.00 |
|