Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam9 |
A |
T |
8: 25,453,026 (GRCm39) |
N760K |
probably benign |
Het |
Ahcyl |
T |
A |
16: 45,974,955 (GRCm39) |
T141S |
probably benign |
Het |
Akr1b10 |
A |
G |
6: 34,369,920 (GRCm39) |
T216A |
possibly damaging |
Het |
Arsj |
A |
G |
3: 126,232,993 (GRCm39) |
R580G |
probably benign |
Het |
C9 |
A |
T |
15: 6,474,918 (GRCm39) |
I26F |
probably damaging |
Het |
Cacna2d1 |
A |
G |
5: 16,533,041 (GRCm39) |
E578G |
probably damaging |
Het |
Clca4b |
C |
T |
3: 144,622,536 (GRCm39) |
V510I |
probably benign |
Het |
Dab2 |
C |
T |
15: 6,464,895 (GRCm39) |
T561I |
possibly damaging |
Het |
Golga5 |
A |
T |
12: 102,450,752 (GRCm39) |
E12D |
possibly damaging |
Het |
Hsd17b12 |
A |
T |
2: 93,874,280 (GRCm39) |
F208I |
probably damaging |
Het |
Inf2 |
A |
G |
12: 112,579,008 (GRCm39) |
|
probably benign |
Het |
Kcnh3 |
T |
A |
15: 99,127,337 (GRCm39) |
W378R |
probably damaging |
Het |
Klhdc8b |
G |
C |
9: 108,326,422 (GRCm39) |
R158G |
possibly damaging |
Het |
Klhl41 |
G |
A |
2: 69,500,554 (GRCm39) |
R5Q |
probably benign |
Het |
Lcn3 |
T |
C |
2: 25,656,421 (GRCm39) |
|
probably null |
Het |
Mppe1 |
A |
G |
18: 67,370,419 (GRCm39) |
|
probably null |
Het |
Muc20 |
G |
A |
16: 32,614,300 (GRCm39) |
A359V |
probably damaging |
Het |
Myh14 |
T |
C |
7: 44,263,105 (GRCm39) |
D1765G |
probably damaging |
Het |
Or10j2 |
T |
C |
1: 173,098,372 (GRCm39) |
M210T |
probably benign |
Het |
Or4c10b |
C |
T |
2: 89,711,235 (GRCm39) |
Q22* |
probably null |
Het |
Or5p58 |
A |
G |
7: 107,693,985 (GRCm39) |
M264T |
probably benign |
Het |
Pbrm1 |
T |
A |
14: 30,757,916 (GRCm39) |
L182Q |
probably damaging |
Het |
Pde8a |
A |
G |
7: 80,967,095 (GRCm39) |
N412S |
probably benign |
Het |
Phyh |
A |
G |
2: 4,940,912 (GRCm39) |
T271A |
probably damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,352,942 (GRCm39) |
S258P |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Pyroxd1 |
A |
G |
6: 142,291,463 (GRCm39) |
E2G |
probably benign |
Het |
Ralgapa1 |
G |
T |
12: 55,723,550 (GRCm39) |
Q2115K |
probably benign |
Het |
Rufy3 |
A |
G |
5: 88,732,129 (GRCm39) |
E44G |
possibly damaging |
Het |
Sptbn1 |
A |
G |
11: 30,095,985 (GRCm39) |
M303T |
possibly damaging |
Het |
Ssbp4 |
A |
G |
8: 71,052,509 (GRCm39) |
I154T |
probably benign |
Het |
Syne2 |
A |
G |
12: 75,977,778 (GRCm39) |
K1409E |
probably benign |
Het |
Tfap2b |
T |
C |
1: 19,304,449 (GRCm39) |
Y420H |
probably damaging |
Het |
Tlr5 |
A |
G |
1: 182,803,261 (GRCm39) |
|
probably null |
Het |
Tmprss15 |
C |
T |
16: 78,821,637 (GRCm39) |
|
probably null |
Het |
Tns1 |
A |
T |
1: 73,959,722 (GRCm39) |
I418N |
probably damaging |
Het |
Txlna |
A |
T |
4: 129,522,984 (GRCm39) |
V452D |
probably benign |
Het |
Wdr17 |
C |
T |
8: 55,146,131 (GRCm39) |
A90T |
possibly damaging |
Het |
Zfp563 |
A |
T |
17: 33,323,659 (GRCm39) |
S85C |
possibly damaging |
Het |
Zfp764l1 |
A |
T |
7: 126,991,504 (GRCm39) |
I161N |
possibly 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 |
|
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 |
|
R4306:Slit2
|
UTSW |
5 |
48,460,125 (GRCm39) |
missense |
possibly damaging |
0.83 |
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 |
|