Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930519P11Rik |
T |
C |
2: 154,454,897 (GRCm39) |
N154S |
unknown |
Het |
Ank3 |
C |
T |
10: 69,828,311 (GRCm39) |
H2327Y |
|
Het |
Ano6 |
A |
G |
15: 95,818,172 (GRCm39) |
Y305C |
probably damaging |
Het |
Apc2 |
A |
G |
10: 80,151,170 (GRCm39) |
T2075A |
possibly damaging |
Het |
Arl6 |
A |
G |
16: 59,443,455 (GRCm39) |
V93A |
possibly damaging |
Het |
Bcas3 |
T |
C |
11: 85,474,763 (GRCm39) |
S790P |
probably damaging |
Het |
Bcl9l |
C |
A |
9: 44,416,448 (GRCm39) |
H211N |
probably benign |
Het |
Bptf |
G |
T |
11: 107,022,233 (GRCm39) |
D172E |
unknown |
Het |
Card9 |
T |
G |
2: 26,249,496 (GRCm39) |
I22L |
possibly damaging |
Het |
Catsperg1 |
C |
A |
7: 28,884,637 (GRCm39) |
G933V |
probably damaging |
Het |
Catsperg2 |
T |
A |
7: 29,404,750 (GRCm39) |
H771L |
possibly damaging |
Het |
Ccdc66 |
T |
C |
14: 27,215,229 (GRCm39) |
N281S |
possibly damaging |
Het |
Cfap54 |
A |
T |
10: 92,612,072 (GRCm39) |
L3162H |
probably damaging |
Het |
Clca4a |
A |
G |
3: 144,663,934 (GRCm39) |
L503P |
probably benign |
Het |
Cpn1 |
T |
C |
19: 43,962,470 (GRCm39) |
N160D |
probably damaging |
Het |
Ctsh |
T |
A |
9: 89,949,154 (GRCm39) |
I206K |
probably benign |
Het |
Cyb561d1 |
G |
A |
3: 108,106,679 (GRCm39) |
T180M |
probably damaging |
Het |
Dapk1 |
A |
T |
13: 60,909,599 (GRCm39) |
D1404V |
probably damaging |
Het |
Dip2c |
G |
T |
13: 9,556,684 (GRCm39) |
R76L |
probably benign |
Het |
Dnah7c |
T |
C |
1: 46,719,898 (GRCm39) |
I2783T |
probably damaging |
Het |
E130308A19Rik |
T |
C |
4: 59,690,333 (GRCm39) |
Y56H |
probably damaging |
Het |
Efemp2 |
G |
T |
19: 5,530,285 (GRCm39) |
A310S |
probably benign |
Het |
Enpp5 |
G |
A |
17: 44,396,155 (GRCm39) |
G356S |
probably damaging |
Het |
Faap24 |
G |
A |
7: 35,092,279 (GRCm39) |
Q213* |
probably null |
Het |
Fam181b |
G |
A |
7: 92,729,943 (GRCm39) |
G239S |
possibly damaging |
Het |
Fancm |
T |
C |
12: 65,148,394 (GRCm39) |
W670R |
probably damaging |
Het |
Fcgbpl1 |
T |
A |
7: 27,853,944 (GRCm39) |
L1636* |
probably null |
Het |
Fmnl1 |
T |
C |
11: 103,081,224 (GRCm39) |
Y357H |
probably damaging |
Het |
Fryl |
A |
T |
5: 73,279,653 (GRCm39) |
V215E |
probably damaging |
Het |
Fscn2 |
C |
A |
11: 120,253,335 (GRCm39) |
N267K |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,816,571 (GRCm39) |
Y4101* |
probably null |
Het |
Gcn1 |
G |
A |
5: 115,728,352 (GRCm39) |
V738I |
probably benign |
Het |
Gdf9 |
C |
T |
11: 53,328,366 (GRCm39) |
R441C |
probably damaging |
Het |
Gipc3 |
C |
T |
10: 81,177,455 (GRCm39) |
G79E |
probably damaging |
Het |
Gzmf |
T |
A |
14: 56,443,391 (GRCm39) |
I196L |
probably benign |
Het |
Hectd1 |
A |
T |
12: 51,806,080 (GRCm39) |
V1852E |
probably damaging |
Het |
Hip1r |
A |
T |
5: 124,134,007 (GRCm39) |
Q256L |
probably benign |
Het |
Hmgxb4 |
T |
C |
8: 75,746,890 (GRCm39) |
S405P |
probably damaging |
Het |
Il9r |
T |
A |
11: 32,142,671 (GRCm39) |
H294L |
probably benign |
Het |
Kif12 |
G |
A |
4: 63,086,931 (GRCm39) |
T331I |
probably damaging |
Het |
Krtap8-1 |
A |
T |
16: 89,284,794 (GRCm39) |
M1K |
probably null |
Het |
Lamc2 |
A |
T |
1: 153,015,495 (GRCm39) |
C613S |
probably damaging |
Het |
Lgr4 |
T |
A |
2: 109,831,314 (GRCm39) |
N314K |
probably benign |
Het |
Lpcat2 |
T |
C |
8: 93,635,894 (GRCm39) |
I432T |
probably benign |
Het |
Mfhas1 |
T |
C |
8: 36,056,146 (GRCm39) |
V207A |
probably benign |
Het |
Msh3 |
T |
G |
13: 92,485,806 (GRCm39) |
T173P |
probably benign |
Het |
Mup15 |
T |
A |
4: 61,356,505 (GRCm39) |
M87L |
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,965,365 (GRCm39) |
V1138A |
probably benign |
Het |
Noc2l |
T |
C |
4: 156,326,179 (GRCm39) |
V422A |
probably benign |
Het |
Notch3 |
C |
T |
17: 32,377,936 (GRCm39) |
G74D |
probably damaging |
Het |
Ocstamp |
T |
A |
2: 165,240,081 (GRCm39) |
K35I |
probably benign |
Het |
Or12k7 |
T |
C |
2: 36,958,400 (GRCm39) |
F28L |
possibly damaging |
Het |
Or52w1 |
A |
G |
7: 105,017,968 (GRCm39) |
H145R |
probably benign |
Het |
Or5p58 |
A |
G |
7: 107,694,342 (GRCm39) |
V145A |
probably benign |
Het |
Or9a2 |
T |
G |
6: 41,748,961 (GRCm39) |
T91P |
probably benign |
Het |
Plekhh2 |
T |
A |
17: 84,829,216 (GRCm39) |
V29D |
probably damaging |
Het |
Pof1b |
A |
G |
X: 111,554,042 (GRCm39) |
I544T |
probably benign |
Het |
Rad54l2 |
C |
T |
9: 106,590,677 (GRCm39) |
R483H |
probably damaging |
Het |
Rapgef6 |
T |
A |
11: 54,567,189 (GRCm39) |
D1128E |
possibly damaging |
Het |
Rhbdl2 |
T |
A |
4: 123,708,049 (GRCm39) |
I86N |
possibly damaging |
Het |
Rims1 |
C |
A |
1: 22,498,740 (GRCm39) |
R68L |
|
Het |
Rnf157 |
A |
G |
11: 116,253,199 (GRCm39) |
F70L |
possibly damaging |
Het |
Rtp3 |
C |
T |
9: 110,815,009 (GRCm39) |
C452Y |
unknown |
Het |
S100a14 |
A |
T |
3: 90,435,069 (GRCm39) |
K27* |
probably null |
Het |
Scai |
C |
T |
2: 38,996,948 (GRCm39) |
G282D |
possibly damaging |
Het |
Serpinf1 |
T |
A |
11: 75,308,811 (GRCm39) |
Q2L |
possibly damaging |
Het |
Skor2 |
T |
A |
18: 76,948,681 (GRCm39) |
V801E |
probably benign |
Het |
Slc16a10 |
C |
G |
10: 39,913,255 (GRCm39) |
E484D |
probably benign |
Het |
Slc1a5 |
T |
A |
7: 16,531,463 (GRCm39) |
D489E |
probably damaging |
Het |
Slx4 |
C |
T |
16: 3,808,650 (GRCm39) |
R430H |
probably benign |
Het |
Teddm1b |
A |
T |
1: 153,750,679 (GRCm39) |
I163F |
probably damaging |
Het |
Tmem171 |
A |
T |
13: 98,828,744 (GRCm39) |
C135* |
probably null |
Het |
Tmem82 |
C |
T |
4: 141,342,284 (GRCm39) |
R306H |
possibly damaging |
Het |
Tmem94 |
T |
A |
11: 115,681,781 (GRCm39) |
|
probably null |
Het |
Trpm2 |
A |
C |
10: 77,759,848 (GRCm39) |
L1096R |
probably damaging |
Het |
Trrap |
T |
A |
5: 144,730,859 (GRCm39) |
L780Q |
probably damaging |
Het |
Txlnb |
A |
G |
10: 17,718,732 (GRCm39) |
D521G |
probably benign |
Het |
Usp7 |
T |
C |
16: 8,534,390 (GRCm39) |
D59G |
probably benign |
Het |
Vcan |
G |
A |
13: 89,873,710 (GRCm39) |
T48I |
probably damaging |
Het |
Vmn1r45 |
A |
G |
6: 89,910,316 (GRCm39) |
L218P |
probably damaging |
Het |
Wdr25 |
A |
T |
12: 108,990,922 (GRCm39) |
T370S |
probably damaging |
Het |
|
Other mutations in Sclt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01069:Sclt1
|
APN |
3 |
41,696,426 (GRCm39) |
unclassified |
probably benign |
|
IGL01106:Sclt1
|
APN |
3 |
41,629,754 (GRCm39) |
splice site |
probably benign |
|
IGL01368:Sclt1
|
APN |
3 |
41,665,610 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02001:Sclt1
|
APN |
3 |
41,636,156 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02897:Sclt1
|
APN |
3 |
41,629,822 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03066:Sclt1
|
APN |
3 |
41,672,278 (GRCm39) |
missense |
probably benign |
0.00 |
R0038:Sclt1
|
UTSW |
3 |
41,583,943 (GRCm39) |
splice site |
probably benign |
|
R0038:Sclt1
|
UTSW |
3 |
41,583,943 (GRCm39) |
splice site |
probably benign |
|
R0172:Sclt1
|
UTSW |
3 |
41,672,222 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0359:Sclt1
|
UTSW |
3 |
41,616,005 (GRCm39) |
critical splice donor site |
probably null |
|
R1281:Sclt1
|
UTSW |
3 |
41,602,055 (GRCm39) |
missense |
probably benign |
0.01 |
R1831:Sclt1
|
UTSW |
3 |
41,681,546 (GRCm39) |
missense |
probably damaging |
0.99 |
R1832:Sclt1
|
UTSW |
3 |
41,681,546 (GRCm39) |
missense |
probably damaging |
0.99 |
R1833:Sclt1
|
UTSW |
3 |
41,681,546 (GRCm39) |
missense |
probably damaging |
0.99 |
R2027:Sclt1
|
UTSW |
3 |
41,685,323 (GRCm39) |
missense |
probably benign |
0.00 |
R4578:Sclt1
|
UTSW |
3 |
41,625,900 (GRCm39) |
nonsense |
probably null |
|
R5502:Sclt1
|
UTSW |
3 |
41,611,710 (GRCm39) |
missense |
probably benign |
0.28 |
R5558:Sclt1
|
UTSW |
3 |
41,616,025 (GRCm39) |
missense |
probably benign |
0.14 |
R5601:Sclt1
|
UTSW |
3 |
41,685,354 (GRCm39) |
missense |
probably benign |
|
R5710:Sclt1
|
UTSW |
3 |
41,618,398 (GRCm39) |
nonsense |
probably null |
|
R6041:Sclt1
|
UTSW |
3 |
41,581,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R6274:Sclt1
|
UTSW |
3 |
41,583,951 (GRCm39) |
critical splice donor site |
probably null |
|
R6765:Sclt1
|
UTSW |
3 |
41,685,337 (GRCm39) |
missense |
unknown |
|
R7489:Sclt1
|
UTSW |
3 |
41,584,032 (GRCm39) |
missense |
probably damaging |
0.99 |
R7988:Sclt1
|
UTSW |
3 |
41,617,889 (GRCm39) |
makesense |
probably null |
|
R8040:Sclt1
|
UTSW |
3 |
41,611,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R8158:Sclt1
|
UTSW |
3 |
41,625,917 (GRCm39) |
missense |
probably benign |
0.36 |
R8383:Sclt1
|
UTSW |
3 |
41,696,450 (GRCm39) |
missense |
probably benign |
0.13 |
R8956:Sclt1
|
UTSW |
3 |
41,636,209 (GRCm39) |
missense |
probably benign |
0.01 |
R8971:Sclt1
|
UTSW |
3 |
41,681,541 (GRCm39) |
missense |
probably benign |
0.01 |
R9227:Sclt1
|
UTSW |
3 |
41,665,631 (GRCm39) |
missense |
probably benign |
0.01 |
R9230:Sclt1
|
UTSW |
3 |
41,665,631 (GRCm39) |
missense |
probably benign |
0.01 |
R9463:Sclt1
|
UTSW |
3 |
41,601,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R9729:Sclt1
|
UTSW |
3 |
41,629,837 (GRCm39) |
nonsense |
probably null |
|
|