Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26b |
C |
G |
8: 43,974,335 (GRCm39) |
M222I |
probably benign |
Het |
Ahnak |
T |
C |
19: 8,992,546 (GRCm39) |
V4610A |
possibly damaging |
Het |
Ankrd13c |
C |
T |
3: 157,653,220 (GRCm39) |
|
silent |
Het |
Cables2 |
A |
G |
2: 179,903,841 (GRCm39) |
|
probably benign |
Het |
Cabp2 |
C |
A |
19: 4,136,497 (GRCm39) |
A181D |
probably damaging |
Het |
Camsap3 |
A |
G |
8: 3,651,999 (GRCm39) |
D265G |
probably damaging |
Het |
Cbs |
G |
T |
17: 31,851,853 (GRCm39) |
T50N |
probably damaging |
Het |
Cenpa |
A |
T |
5: 30,830,381 (GRCm39) |
Q83L |
possibly damaging |
Het |
Cit |
A |
T |
5: 116,063,598 (GRCm39) |
|
probably benign |
Het |
Ckap5 |
A |
G |
2: 91,445,445 (GRCm39) |
E1694G |
possibly damaging |
Het |
Copz1 |
A |
T |
15: 103,203,197 (GRCm39) |
M104L |
probably benign |
Het |
Crot |
T |
A |
5: 9,024,192 (GRCm39) |
M335L |
probably benign |
Het |
Ctnna2 |
T |
C |
6: 77,120,904 (GRCm39) |
D373G |
probably benign |
Het |
Ctu2 |
G |
A |
8: 123,203,693 (GRCm39) |
|
probably benign |
Het |
Cyp3a59 |
T |
A |
5: 146,027,455 (GRCm39) |
Y75* |
probably null |
Het |
Dbi |
A |
G |
1: 120,048,583 (GRCm39) |
I21T |
probably benign |
Het |
Dcun1d3 |
A |
G |
7: 119,458,799 (GRCm39) |
S79P |
probably benign |
Het |
Dock10 |
T |
A |
1: 80,483,304 (GRCm39) |
|
probably benign |
Het |
Dstyk |
T |
A |
1: 132,381,875 (GRCm39) |
I543N |
probably damaging |
Het |
Epx |
G |
T |
11: 87,756,318 (GRCm39) |
A621E |
probably damaging |
Het |
Farp2 |
G |
A |
1: 93,548,367 (GRCm39) |
|
probably null |
Het |
Gm11992 |
C |
T |
11: 9,002,711 (GRCm39) |
P25S |
probably damaging |
Het |
Grik5 |
A |
T |
7: 24,758,502 (GRCm39) |
M307K |
possibly damaging |
Het |
Hnf1b |
A |
T |
11: 83,773,503 (GRCm39) |
N234I |
probably damaging |
Het |
Htr2a |
A |
G |
14: 74,882,530 (GRCm39) |
D172G |
probably damaging |
Het |
Ifit1bl2 |
T |
C |
19: 34,597,128 (GRCm39) |
T163A |
probably benign |
Het |
Igsf10 |
A |
T |
3: 59,235,578 (GRCm39) |
D1534E |
probably benign |
Het |
Il3ra |
T |
G |
14: 14,350,799 (GRCm38) |
V178G |
probably damaging |
Het |
Itgb1 |
A |
T |
8: 129,439,718 (GRCm39) |
K136* |
probably null |
Het |
Itprid1 |
A |
T |
6: 55,874,754 (GRCm39) |
R235* |
probably null |
Het |
Lama2 |
T |
A |
10: 26,891,494 (GRCm39) |
I2540F |
probably benign |
Het |
Lrp8 |
C |
A |
4: 107,714,493 (GRCm39) |
H622Q |
probably damaging |
Het |
Lrrc2 |
T |
A |
9: 110,795,629 (GRCm39) |
M138K |
probably benign |
Het |
Lrrk2 |
C |
A |
15: 91,630,034 (GRCm39) |
H1242N |
probably benign |
Het |
Lsm11 |
G |
C |
11: 45,835,445 (GRCm39) |
R99G |
probably benign |
Het |
Mif4gd |
C |
T |
11: 115,500,439 (GRCm39) |
V40M |
probably benign |
Het |
Mpp3 |
A |
T |
11: 101,916,241 (GRCm39) |
V37D |
probably damaging |
Het |
Mre11a |
T |
A |
9: 14,698,258 (GRCm39) |
D35E |
probably damaging |
Het |
Mroh4 |
C |
A |
15: 74,493,003 (GRCm39) |
V233F |
probably damaging |
Het |
Npy2r |
A |
T |
3: 82,448,068 (GRCm39) |
S123T |
possibly damaging |
Het |
Nrip2 |
A |
G |
6: 128,385,361 (GRCm39) |
Y264C |
possibly damaging |
Het |
Obscn |
A |
G |
11: 58,897,639 (GRCm39) |
S6639P |
unknown |
Het |
Or10d4 |
C |
T |
9: 39,580,386 (GRCm39) |
T11I |
probably benign |
Het |
Or51t4 |
T |
A |
7: 102,598,017 (GRCm39) |
F105Y |
probably benign |
Het |
Osbpl5 |
C |
T |
7: 143,310,695 (GRCm39) |
|
probably benign |
Het |
Panx1 |
A |
T |
9: 14,921,513 (GRCm39) |
Y121N |
probably damaging |
Het |
Pcdhb8 |
A |
G |
18: 37,489,243 (GRCm39) |
D307G |
probably damaging |
Het |
Pde1b |
A |
G |
15: 103,429,866 (GRCm39) |
K120E |
possibly damaging |
Het |
Pdzrn4 |
T |
C |
15: 92,295,255 (GRCm39) |
S154P |
probably benign |
Het |
Ppp1r13b |
T |
C |
12: 111,796,876 (GRCm39) |
K889R |
probably benign |
Het |
Ppp4r3a |
T |
A |
12: 101,017,872 (GRCm39) |
D439V |
probably damaging |
Het |
Ptk2b |
A |
G |
14: 66,411,328 (GRCm39) |
I401T |
probably damaging |
Het |
Rab24 |
T |
C |
13: 55,468,343 (GRCm39) |
T153A |
probably damaging |
Het |
Rarb |
C |
A |
14: 16,434,264 (GRCm38) |
A305S |
probably damaging |
Het |
Rc3h2 |
GCC |
GCCC |
2: 37,304,745 (GRCm39) |
|
probably null |
Het |
Scn10a |
G |
A |
9: 119,456,237 (GRCm39) |
T1194I |
probably damaging |
Het |
Scn3a |
G |
T |
2: 65,295,180 (GRCm39) |
N1514K |
probably damaging |
Het |
Shisa5 |
T |
A |
9: 108,885,751 (GRCm39) |
M229K |
possibly damaging |
Het |
Sik2 |
C |
T |
9: 50,828,431 (GRCm39) |
G204R |
probably damaging |
Het |
Sla |
C |
T |
15: 66,665,554 (GRCm39) |
G46E |
probably damaging |
Het |
Slc35g3 |
A |
T |
11: 69,652,509 (GRCm39) |
M1K |
probably null |
Het |
Slc5a7 |
A |
T |
17: 54,583,972 (GRCm39) |
Y439* |
probably null |
Het |
Slc9a1 |
T |
C |
4: 133,147,176 (GRCm39) |
|
probably benign |
Het |
Slitrk6 |
T |
G |
14: 110,987,305 (GRCm39) |
T801P |
probably benign |
Het |
Spata31d1c |
T |
C |
13: 65,184,894 (GRCm39) |
V812A |
possibly damaging |
Het |
Spata31g1 |
T |
C |
4: 42,971,465 (GRCm39) |
L230P |
probably benign |
Het |
Spef1l |
G |
A |
7: 139,556,526 (GRCm39) |
H154Y |
probably benign |
Het |
Sphkap |
A |
C |
1: 83,317,320 (GRCm39) |
L59R |
probably damaging |
Het |
Spmip8 |
A |
T |
8: 96,046,620 (GRCm39) |
T98S |
possibly damaging |
Het |
Srsf10 |
C |
A |
4: 135,583,553 (GRCm39) |
R6S |
probably damaging |
Het |
Supt5 |
T |
A |
7: 28,028,900 (GRCm39) |
R131S |
probably benign |
Het |
Syne1 |
T |
C |
10: 5,310,706 (GRCm39) |
|
probably null |
Het |
Tet2 |
T |
A |
3: 133,194,296 (GRCm39) |
H46L |
possibly damaging |
Het |
Tnfsf4 |
T |
A |
1: 161,244,819 (GRCm39) |
N169K |
probably damaging |
Het |
Tprg1 |
A |
T |
16: 25,136,011 (GRCm39) |
M1L |
possibly damaging |
Het |
Tsen2 |
A |
G |
6: 115,536,556 (GRCm39) |
Y104C |
probably damaging |
Het |
Ttc6 |
A |
G |
12: 57,720,590 (GRCm39) |
Y952C |
probably damaging |
Het |
Umod |
A |
T |
7: 119,070,650 (GRCm39) |
I414N |
probably damaging |
Het |
Usp10 |
G |
T |
8: 120,673,828 (GRCm39) |
V398L |
possibly damaging |
Het |
Vmn2r23 |
A |
T |
6: 123,718,854 (GRCm39) |
I736F |
possibly damaging |
Het |
Vmn2r65 |
C |
A |
7: 84,592,869 (GRCm39) |
G446V |
probably benign |
Het |
Wbp1l |
C |
T |
19: 46,642,619 (GRCm39) |
R191* |
probably null |
Het |
Yars2 |
A |
G |
16: 16,127,335 (GRCm39) |
I467V |
probably benign |
Het |
Ykt6 |
A |
G |
11: 5,909,338 (GRCm39) |
E49G |
possibly damaging |
Het |
Zan |
T |
A |
5: 137,442,192 (GRCm39) |
M1907L |
unknown |
Het |
Zdhhc2 |
T |
C |
8: 40,917,277 (GRCm39) |
S225P |
probably damaging |
Het |
Zfc3h1 |
A |
T |
10: 115,267,262 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Serpinb3d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01582:Serpinb3d
|
APN |
1 |
107,007,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01917:Serpinb3d
|
APN |
1 |
107,007,411 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02732:Serpinb3d
|
APN |
1 |
107,010,526 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02988:Serpinb3d
|
UTSW |
1 |
107,006,266 (GRCm39) |
missense |
probably benign |
|
R0540:Serpinb3d
|
UTSW |
1 |
107,006,962 (GRCm39) |
missense |
probably benign |
0.01 |
R0594:Serpinb3d
|
UTSW |
1 |
107,007,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R1666:Serpinb3d
|
UTSW |
1 |
107,008,481 (GRCm39) |
missense |
probably benign |
0.18 |
R1668:Serpinb3d
|
UTSW |
1 |
107,008,481 (GRCm39) |
missense |
probably benign |
0.18 |
R1905:Serpinb3d
|
UTSW |
1 |
107,007,014 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1994:Serpinb3d
|
UTSW |
1 |
107,008,518 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2021:Serpinb3d
|
UTSW |
1 |
107,006,182 (GRCm39) |
missense |
probably benign |
0.05 |
R2022:Serpinb3d
|
UTSW |
1 |
107,006,182 (GRCm39) |
missense |
probably benign |
0.05 |
R3760:Serpinb3d
|
UTSW |
1 |
107,009,304 (GRCm39) |
splice site |
probably benign |
|
R4118:Serpinb3d
|
UTSW |
1 |
107,006,960 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4496:Serpinb3d
|
UTSW |
1 |
107,007,022 (GRCm39) |
missense |
probably damaging |
0.98 |
R4770:Serpinb3d
|
UTSW |
1 |
107,006,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R4793:Serpinb3d
|
UTSW |
1 |
107,005,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Serpinb3d
|
UTSW |
1 |
107,006,228 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5434:Serpinb3d
|
UTSW |
1 |
107,006,263 (GRCm39) |
missense |
probably benign |
0.02 |
R5813:Serpinb3d
|
UTSW |
1 |
107,007,027 (GRCm39) |
missense |
probably benign |
0.14 |
R5820:Serpinb3d
|
UTSW |
1 |
107,006,089 (GRCm39) |
missense |
probably damaging |
0.99 |
R6056:Serpinb3d
|
UTSW |
1 |
107,007,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R6092:Serpinb3d
|
UTSW |
1 |
107,006,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R6188:Serpinb3d
|
UTSW |
1 |
107,006,237 (GRCm39) |
missense |
probably damaging |
0.98 |
R6247:Serpinb3d
|
UTSW |
1 |
107,010,490 (GRCm39) |
missense |
probably benign |
0.01 |
R6369:Serpinb3d
|
UTSW |
1 |
107,008,483 (GRCm39) |
missense |
probably benign |
0.00 |
R6476:Serpinb3d
|
UTSW |
1 |
107,011,071 (GRCm39) |
missense |
probably benign |
0.09 |
R7178:Serpinb3d
|
UTSW |
1 |
107,008,506 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7743:Serpinb3d
|
UTSW |
1 |
107,007,088 (GRCm39) |
missense |
probably damaging |
0.99 |
R7765:Serpinb3d
|
UTSW |
1 |
107,007,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R8371:Serpinb3d
|
UTSW |
1 |
107,008,469 (GRCm39) |
missense |
probably damaging |
1.00 |
|