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 |
Serpinb3d |
T |
C |
1: 107,011,105 (GRCm39) |
T36A |
probably benign |
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 |
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 Vmn2r65 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00942:Vmn2r65
|
APN |
7 |
84,592,761 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01104:Vmn2r65
|
APN |
7 |
84,589,996 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01154:Vmn2r65
|
APN |
7 |
84,592,729 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01453:Vmn2r65
|
APN |
7 |
84,589,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01675:Vmn2r65
|
APN |
7 |
84,596,587 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01748:Vmn2r65
|
APN |
7 |
84,589,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01997:Vmn2r65
|
APN |
7 |
84,589,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02527:Vmn2r65
|
APN |
7 |
84,595,724 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02617:Vmn2r65
|
APN |
7 |
84,589,549 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02676:Vmn2r65
|
APN |
7 |
84,589,381 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03084:Vmn2r65
|
APN |
7 |
84,592,354 (GRCm39) |
missense |
probably damaging |
1.00 |
A4554:Vmn2r65
|
UTSW |
7 |
84,595,791 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4651001:Vmn2r65
|
UTSW |
7 |
84,595,461 (GRCm39) |
missense |
probably benign |
0.12 |
R0322:Vmn2r65
|
UTSW |
7 |
84,595,756 (GRCm39) |
missense |
probably benign |
0.01 |
R0453:Vmn2r65
|
UTSW |
7 |
84,595,442 (GRCm39) |
missense |
probably benign |
0.03 |
R0862:Vmn2r65
|
UTSW |
7 |
84,592,853 (GRCm39) |
missense |
probably benign |
0.00 |
R1392:Vmn2r65
|
UTSW |
7 |
84,596,624 (GRCm39) |
missense |
probably benign |
0.14 |
R1392:Vmn2r65
|
UTSW |
7 |
84,596,624 (GRCm39) |
missense |
probably benign |
0.14 |
R1508:Vmn2r65
|
UTSW |
7 |
84,589,886 (GRCm39) |
missense |
probably benign |
0.00 |
R1687:Vmn2r65
|
UTSW |
7 |
84,590,026 (GRCm39) |
missense |
probably benign |
0.02 |
R1876:Vmn2r65
|
UTSW |
7 |
84,595,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R2136:Vmn2r65
|
UTSW |
7 |
84,592,781 (GRCm39) |
missense |
probably damaging |
0.96 |
R2259:Vmn2r65
|
UTSW |
7 |
84,590,119 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2338:Vmn2r65
|
UTSW |
7 |
84,590,051 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2880:Vmn2r65
|
UTSW |
7 |
84,613,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R3410:Vmn2r65
|
UTSW |
7 |
84,595,896 (GRCm39) |
missense |
probably benign |
0.00 |
R3411:Vmn2r65
|
UTSW |
7 |
84,595,896 (GRCm39) |
missense |
probably benign |
0.00 |
R3770:Vmn2r65
|
UTSW |
7 |
84,589,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R3800:Vmn2r65
|
UTSW |
7 |
84,589,738 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3850:Vmn2r65
|
UTSW |
7 |
84,595,859 (GRCm39) |
missense |
probably benign |
0.00 |
R4105:Vmn2r65
|
UTSW |
7 |
84,595,691 (GRCm39) |
missense |
probably benign |
0.03 |
R4568:Vmn2r65
|
UTSW |
7 |
84,596,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R4677:Vmn2r65
|
UTSW |
7 |
84,613,082 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4768:Vmn2r65
|
UTSW |
7 |
84,596,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R4778:Vmn2r65
|
UTSW |
7 |
84,592,801 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5057:Vmn2r65
|
UTSW |
7 |
84,589,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R5279:Vmn2r65
|
UTSW |
7 |
84,589,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R5280:Vmn2r65
|
UTSW |
7 |
84,595,542 (GRCm39) |
missense |
probably damaging |
0.99 |
R5394:Vmn2r65
|
UTSW |
7 |
84,595,862 (GRCm39) |
missense |
probably benign |
0.04 |
R5487:Vmn2r65
|
UTSW |
7 |
84,595,529 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5580:Vmn2r65
|
UTSW |
7 |
84,596,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R5638:Vmn2r65
|
UTSW |
7 |
84,590,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R5673:Vmn2r65
|
UTSW |
7 |
84,596,615 (GRCm39) |
missense |
probably benign |
0.23 |
R5688:Vmn2r65
|
UTSW |
7 |
84,589,900 (GRCm39) |
missense |
probably benign |
0.00 |
R6354:Vmn2r65
|
UTSW |
7 |
84,589,574 (GRCm39) |
missense |
probably benign |
0.35 |
R6372:Vmn2r65
|
UTSW |
7 |
84,589,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R6924:Vmn2r65
|
UTSW |
7 |
84,613,198 (GRCm39) |
missense |
probably benign |
0.20 |
R7021:Vmn2r65
|
UTSW |
7 |
84,596,587 (GRCm39) |
missense |
probably benign |
0.00 |
R7195:Vmn2r65
|
UTSW |
7 |
84,592,347 (GRCm39) |
critical splice donor site |
probably null |
|
R7422:Vmn2r65
|
UTSW |
7 |
84,595,569 (GRCm39) |
missense |
probably damaging |
0.99 |
R7654:Vmn2r65
|
UTSW |
7 |
84,590,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R7686:Vmn2r65
|
UTSW |
7 |
84,589,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R7691:Vmn2r65
|
UTSW |
7 |
84,592,851 (GRCm39) |
missense |
probably benign |
0.30 |
R7798:Vmn2r65
|
UTSW |
7 |
84,596,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R7798:Vmn2r65
|
UTSW |
7 |
84,595,530 (GRCm39) |
missense |
probably benign |
0.00 |
R8103:Vmn2r65
|
UTSW |
7 |
84,595,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R8272:Vmn2r65
|
UTSW |
7 |
84,596,817 (GRCm39) |
missense |
probably benign |
0.02 |
R8303:Vmn2r65
|
UTSW |
7 |
84,589,391 (GRCm39) |
nonsense |
probably null |
|
R8354:Vmn2r65
|
UTSW |
7 |
84,589,402 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8454:Vmn2r65
|
UTSW |
7 |
84,589,402 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8489:Vmn2r65
|
UTSW |
7 |
84,589,964 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8554:Vmn2r65
|
UTSW |
7 |
84,595,960 (GRCm39) |
missense |
probably benign |
0.00 |
R8680:Vmn2r65
|
UTSW |
7 |
84,589,388 (GRCm39) |
missense |
probably benign |
0.00 |
R8731:Vmn2r65
|
UTSW |
7 |
84,589,447 (GRCm39) |
nonsense |
probably null |
|
R8839:Vmn2r65
|
UTSW |
7 |
84,595,489 (GRCm39) |
nonsense |
probably null |
|
R8847:Vmn2r65
|
UTSW |
7 |
84,590,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R8916:Vmn2r65
|
UTSW |
7 |
84,595,665 (GRCm39) |
missense |
probably benign |
0.21 |
R9254:Vmn2r65
|
UTSW |
7 |
84,596,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R9379:Vmn2r65
|
UTSW |
7 |
84,596,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R9392:Vmn2r65
|
UTSW |
7 |
84,589,718 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9563:Vmn2r65
|
UTSW |
7 |
84,589,880 (GRCm39) |
nonsense |
probably null |
|
R9686:Vmn2r65
|
UTSW |
7 |
84,590,084 (GRCm39) |
missense |
probably benign |
0.45 |
X0067:Vmn2r65
|
UTSW |
7 |
84,590,113 (GRCm39) |
missense |
probably benign |
0.04 |
Z1088:Vmn2r65
|
UTSW |
7 |
84,592,473 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Vmn2r65
|
UTSW |
7 |
84,590,234 (GRCm39) |
missense |
probably damaging |
0.97 |
|