Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox1 |
T |
A |
1: 58,145,184 (GRCm39) |
|
probably null |
Het |
Aspm |
C |
T |
1: 139,410,182 (GRCm39) |
T1359I |
probably benign |
Het |
Atp13a2 |
A |
G |
4: 140,719,509 (GRCm39) |
D26G |
probably benign |
Het |
Atrnl1 |
G |
A |
19: 58,119,536 (GRCm39) |
A1343T |
probably damaging |
Het |
Ccsap |
A |
C |
8: 124,585,969 (GRCm39) |
S61A |
probably damaging |
Het |
Cdh1 |
A |
T |
8: 107,384,485 (GRCm39) |
M318L |
probably benign |
Het |
Cfap69 |
G |
A |
5: 5,696,979 (GRCm39) |
P106S |
probably damaging |
Het |
Cfp |
G |
A |
X: 20,795,963 (GRCm39) |
T88I |
probably damaging |
Het |
Chst1 |
A |
T |
2: 92,444,475 (GRCm39) |
I316F |
probably damaging |
Het |
Col7a1 |
A |
T |
9: 108,793,686 (GRCm39) |
D1382V |
unknown |
Het |
Cr2 |
T |
A |
1: 194,845,542 (GRCm39) |
M514L |
possibly damaging |
Het |
Cubn |
G |
A |
2: 13,470,719 (GRCm39) |
H558Y |
probably benign |
Het |
Cul9 |
A |
T |
17: 46,839,572 (GRCm39) |
M802K |
probably damaging |
Het |
Dennd2d |
A |
T |
3: 106,398,542 (GRCm39) |
I169L |
probably damaging |
Het |
Dnah11 |
T |
A |
12: 118,010,991 (GRCm39) |
K162* |
probably null |
Het |
Dnah3 |
T |
A |
7: 119,566,943 (GRCm39) |
T2428S |
possibly damaging |
Het |
Dock11 |
T |
A |
X: 35,301,296 (GRCm39) |
H1284Q |
probably damaging |
Het |
Flrt2 |
T |
A |
12: 95,745,966 (GRCm39) |
D101E |
probably damaging |
Het |
Gabrr2 |
G |
A |
4: 33,085,626 (GRCm39) |
V349M |
probably damaging |
Het |
Gli2 |
C |
A |
1: 118,764,621 (GRCm39) |
V1177L |
probably benign |
Het |
Gm16506 |
A |
G |
14: 43,961,630 (GRCm39) |
Y206H |
probably benign |
Het |
Gm5612 |
C |
T |
9: 18,338,869 (GRCm39) |
|
probably benign |
Het |
Gvin3 |
C |
T |
7: 106,202,258 (GRCm39) |
|
noncoding transcript |
Het |
Heg1 |
C |
T |
16: 33,545,936 (GRCm39) |
T460I |
possibly damaging |
Het |
Lgals9 |
T |
G |
11: 78,863,977 (GRCm39) |
D56A |
probably damaging |
Het |
Lpgat1 |
A |
T |
1: 191,508,544 (GRCm39) |
|
probably null |
Het |
Megf6 |
T |
A |
4: 154,337,020 (GRCm39) |
|
probably null |
Het |
Megf8 |
G |
A |
7: 25,059,296 (GRCm39) |
M2265I |
probably benign |
Het |
Memo1 |
G |
A |
17: 74,548,976 (GRCm39) |
R121* |
probably null |
Het |
Morc1 |
T |
C |
16: 48,432,677 (GRCm39) |
V715A |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,466,928 (GRCm39) |
|
probably null |
Het |
Ncapg2 |
T |
A |
12: 116,388,270 (GRCm39) |
V318D |
possibly damaging |
Het |
Ndst1 |
T |
C |
18: 60,833,517 (GRCm39) |
Y498C |
probably damaging |
Het |
Nod1 |
C |
T |
6: 54,921,341 (GRCm39) |
A326T |
probably damaging |
Het |
Or2ag15 |
A |
G |
7: 106,340,706 (GRCm39) |
V145A |
probably benign |
Het |
Or4c11 |
T |
A |
2: 88,695,864 (GRCm39) |
M305K |
probably benign |
Het |
Peg3 |
T |
C |
7: 6,710,624 (GRCm39) |
S1533G |
probably benign |
Het |
Pgc |
G |
T |
17: 48,045,165 (GRCm39) |
G361V |
probably damaging |
Het |
Phka1 |
C |
T |
X: 101,629,712 (GRCm39) |
R477H |
probably damaging |
Het |
Plagl2 |
C |
T |
2: 153,074,574 (GRCm39) |
R109Q |
probably damaging |
Het |
Prr36 |
T |
A |
8: 4,266,230 (GRCm39) |
I107F |
probably benign |
Het |
Ptpdc1 |
T |
A |
13: 48,740,080 (GRCm39) |
R450S |
probably damaging |
Het |
Ptprb |
A |
T |
10: 116,138,179 (GRCm39) |
D361V |
possibly damaging |
Het |
Rbm44 |
A |
G |
1: 91,096,551 (GRCm39) |
D970G |
probably benign |
Het |
Scrn2 |
T |
G |
11: 96,921,396 (GRCm39) |
V52G |
probably benign |
Het |
Sdk1 |
C |
T |
5: 142,197,875 (GRCm39) |
T2176I |
probably benign |
Het |
Serpina1d |
T |
A |
12: 103,729,993 (GRCm39) |
E396D |
probably benign |
Het |
Slc38a5 |
A |
C |
X: 8,146,070 (GRCm39) |
Q465P |
probably benign |
Het |
Slc38a5 |
G |
T |
X: 8,146,071 (GRCm39) |
Q465H |
probably benign |
Het |
Smarca1 |
T |
C |
X: 46,981,255 (GRCm39) |
T48A |
possibly damaging |
Het |
Trak2 |
A |
T |
1: 58,962,766 (GRCm39) |
I132N |
probably damaging |
Het |
Trank1 |
A |
G |
9: 111,194,117 (GRCm39) |
T714A |
probably benign |
Het |
Trank1 |
T |
C |
9: 111,194,327 (GRCm39) |
S784P |
probably benign |
Het |
Trp53i13 |
G |
A |
11: 77,399,083 (GRCm39) |
|
probably benign |
Het |
Trrap |
A |
C |
5: 144,767,831 (GRCm39) |
D2596A |
probably benign |
Het |
Ttyh1 |
A |
T |
7: 4,127,656 (GRCm39) |
T19S |
probably damaging |
Het |
Tyk2 |
C |
T |
9: 21,020,660 (GRCm39) |
V947M |
probably damaging |
Het |
Ugt2b34 |
G |
A |
5: 87,040,689 (GRCm39) |
A411V |
possibly damaging |
Het |
Virma |
T |
A |
4: 11,518,929 (GRCm39) |
Y725* |
probably null |
Het |
Vmn2r74 |
T |
C |
7: 85,610,500 (GRCm39) |
D64G |
possibly damaging |
Het |
|
Other mutations in Vmn1r192 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01869:Vmn1r192
|
APN |
13 |
22,371,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R0975:Vmn1r192
|
UTSW |
13 |
22,371,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Vmn1r192
|
UTSW |
13 |
22,371,441 (GRCm39) |
missense |
probably benign |
0.08 |
R1767:Vmn1r192
|
UTSW |
13 |
22,371,441 (GRCm39) |
missense |
probably benign |
0.08 |
R1880:Vmn1r192
|
UTSW |
13 |
22,371,764 (GRCm39) |
missense |
probably benign |
0.12 |
R1881:Vmn1r192
|
UTSW |
13 |
22,371,764 (GRCm39) |
missense |
probably benign |
0.12 |
R2113:Vmn1r192
|
UTSW |
13 |
22,371,800 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4290:Vmn1r192
|
UTSW |
13 |
22,371,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R4292:Vmn1r192
|
UTSW |
13 |
22,371,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R4294:Vmn1r192
|
UTSW |
13 |
22,371,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R4295:Vmn1r192
|
UTSW |
13 |
22,371,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R4921:Vmn1r192
|
UTSW |
13 |
22,371,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R5377:Vmn1r192
|
UTSW |
13 |
22,371,801 (GRCm39) |
missense |
probably benign |
0.01 |
R5569:Vmn1r192
|
UTSW |
13 |
22,371,384 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6181:Vmn1r192
|
UTSW |
13 |
22,371,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R6455:Vmn1r192
|
UTSW |
13 |
22,372,000 (GRCm39) |
missense |
probably benign |
0.08 |
R6860:Vmn1r192
|
UTSW |
13 |
22,372,122 (GRCm39) |
missense |
probably benign |
|
R7246:Vmn1r192
|
UTSW |
13 |
22,371,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R7762:Vmn1r192
|
UTSW |
13 |
22,371,845 (GRCm39) |
missense |
probably damaging |
0.97 |
R8066:Vmn1r192
|
UTSW |
13 |
22,371,565 (GRCm39) |
nonsense |
probably null |
|
R8378:Vmn1r192
|
UTSW |
13 |
22,372,029 (GRCm39) |
nonsense |
probably null |
|
R9075:Vmn1r192
|
UTSW |
13 |
22,371,333 (GRCm39) |
missense |
probably benign |
|
R9206:Vmn1r192
|
UTSW |
13 |
22,371,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R9208:Vmn1r192
|
UTSW |
13 |
22,371,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R9313:Vmn1r192
|
UTSW |
13 |
22,372,191 (GRCm39) |
missense |
probably benign |
0.38 |
R9367:Vmn1r192
|
UTSW |
13 |
22,371,800 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9694:Vmn1r192
|
UTSW |
13 |
22,372,119 (GRCm39) |
missense |
probably benign |
|
R9760:Vmn1r192
|
UTSW |
13 |
22,372,010 (GRCm39) |
missense |
probably damaging |
1.00 |
|