Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap6 |
T |
A |
12: 52,958,591 (GRCm39) |
V782E |
probably damaging |
Het |
Atg9a |
A |
G |
1: 75,161,734 (GRCm39) |
L604P |
probably damaging |
Het |
Atp1a3 |
T |
C |
7: 24,689,974 (GRCm39) |
I482V |
probably benign |
Het |
Bltp2 |
T |
G |
11: 78,178,813 (GRCm39) |
M2026R |
probably damaging |
Het |
Bltp2 |
T |
A |
11: 78,168,038 (GRCm39) |
L1491* |
probably null |
Het |
Ccdc18 |
T |
G |
5: 108,311,530 (GRCm39) |
V412G |
probably benign |
Het |
Ccn6 |
T |
C |
10: 39,027,285 (GRCm39) |
R316G |
probably benign |
Het |
Cct6a |
A |
G |
5: 129,871,449 (GRCm39) |
|
noncoding transcript |
Het |
Clpx |
A |
G |
9: 65,217,507 (GRCm39) |
N25S |
probably damaging |
Het |
Cnpy2 |
T |
A |
10: 128,162,894 (GRCm39) |
C171* |
probably null |
Het |
Cntnap3 |
C |
T |
13: 64,905,211 (GRCm39) |
D857N |
probably damaging |
Het |
Col5a1 |
A |
G |
2: 27,922,697 (GRCm39) |
Y255C |
probably damaging |
Het |
Coro7 |
A |
T |
16: 4,449,775 (GRCm39) |
F638Y |
possibly damaging |
Het |
Cpd |
A |
G |
11: 76,673,153 (GRCm39) |
F1331L |
probably damaging |
Het |
Csmd1 |
A |
T |
8: 16,119,063 (GRCm39) |
I1842N |
possibly damaging |
Het |
Dgkg |
T |
A |
16: 22,381,480 (GRCm39) |
D490V |
probably damaging |
Het |
Dnah9 |
A |
T |
11: 65,976,284 (GRCm39) |
M1255K |
probably benign |
Het |
E2f1 |
A |
G |
2: 154,402,849 (GRCm39) |
V306A |
probably benign |
Het |
Entpd1 |
A |
G |
19: 40,648,350 (GRCm39) |
|
probably benign |
Het |
Esrrb |
T |
A |
12: 86,552,676 (GRCm39) |
I222N |
probably benign |
Het |
Flt4 |
G |
T |
11: 49,516,274 (GRCm39) |
A126S |
possibly damaging |
Het |
Galnt11 |
C |
T |
5: 25,457,145 (GRCm39) |
T237I |
possibly damaging |
Het |
Galnt2l |
A |
T |
8: 122,997,727 (GRCm39) |
|
probably benign |
Het |
Gbf1 |
A |
G |
19: 46,250,983 (GRCm39) |
|
probably benign |
Het |
H2-T9 |
T |
C |
17: 36,438,726 (GRCm39) |
T222A |
possibly damaging |
Het |
Herc1 |
T |
A |
9: 66,392,170 (GRCm39) |
|
probably benign |
Het |
Hsph1 |
T |
C |
5: 149,554,967 (GRCm39) |
Y105C |
probably damaging |
Het |
Il23r |
T |
C |
6: 67,411,664 (GRCm39) |
T358A |
probably benign |
Het |
Il2ra |
C |
T |
2: 11,647,884 (GRCm39) |
|
probably benign |
Het |
Kbtbd4 |
G |
T |
2: 90,744,459 (GRCm39) |
|
probably benign |
Het |
Kcnt1 |
A |
G |
2: 25,781,255 (GRCm39) |
|
probably benign |
Het |
Kng2 |
A |
G |
16: 22,815,872 (GRCm39) |
|
probably benign |
Het |
Lap3 |
C |
T |
5: 45,669,270 (GRCm39) |
T473I |
possibly damaging |
Het |
Lrrk2 |
T |
C |
15: 91,641,273 (GRCm39) |
|
probably null |
Het |
Map1s |
A |
G |
8: 71,366,696 (GRCm39) |
N534D |
possibly damaging |
Het |
Mtg1 |
G |
A |
7: 139,724,257 (GRCm39) |
V122I |
probably benign |
Het |
Myadm |
T |
A |
7: 3,345,865 (GRCm39) |
I209K |
probably damaging |
Het |
Ntsr2 |
G |
A |
12: 16,703,981 (GRCm39) |
V75I |
probably benign |
Het |
Or4b1b |
A |
T |
2: 90,112,212 (GRCm39) |
S236T |
probably damaging |
Het |
Or8u10 |
G |
A |
2: 85,915,557 (GRCm39) |
A188V |
probably benign |
Het |
Pfn1 |
T |
C |
11: 70,545,192 (GRCm39) |
T39A |
probably benign |
Het |
Pipox |
T |
A |
11: 77,774,651 (GRCm39) |
K144M |
probably benign |
Het |
Plekhh1 |
G |
A |
12: 79,115,889 (GRCm39) |
E811K |
probably damaging |
Het |
Pnpla3 |
T |
A |
15: 84,063,506 (GRCm39) |
W295R |
probably benign |
Het |
Prkacb |
T |
A |
3: 146,457,273 (GRCm39) |
T136S |
probably damaging |
Het |
Ralbp1 |
T |
A |
17: 66,161,124 (GRCm39) |
N473I |
probably benign |
Het |
Rbp4 |
G |
A |
19: 38,106,908 (GRCm39) |
T127M |
probably damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rps3a1 |
G |
A |
3: 86,045,424 (GRCm39) |
|
probably benign |
Het |
Scg3 |
G |
T |
9: 75,551,222 (GRCm39) |
Y429* |
probably null |
Het |
Shisal2b |
G |
T |
13: 104,994,862 (GRCm39) |
T95K |
possibly damaging |
Het |
Spag5 |
T |
C |
11: 78,204,222 (GRCm39) |
S492P |
probably damaging |
Het |
St7 |
T |
A |
6: 17,934,238 (GRCm39) |
M540K |
probably damaging |
Het |
Stxbp3 |
C |
A |
3: 108,712,618 (GRCm39) |
V281F |
possibly damaging |
Het |
Sun5 |
A |
G |
2: 153,700,968 (GRCm39) |
V242A |
possibly damaging |
Het |
Susd5 |
G |
T |
9: 113,924,852 (GRCm39) |
R245L |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 75,969,787 (GRCm39) |
E954G |
probably damaging |
Het |
Synpo2 |
A |
T |
3: 122,907,708 (GRCm39) |
V536E |
probably damaging |
Het |
Tas2r140 |
T |
C |
6: 133,032,405 (GRCm39) |
I118V |
probably benign |
Het |
Tbx18 |
C |
A |
9: 87,606,462 (GRCm39) |
V228L |
probably benign |
Het |
Tdrd9 |
T |
A |
12: 111,974,014 (GRCm39) |
|
probably benign |
Het |
Tektl1 |
C |
A |
10: 78,586,381 (GRCm39) |
L223F |
probably benign |
Het |
Tg |
T |
C |
15: 66,609,370 (GRCm39) |
M310T |
probably benign |
Het |
Ticam2 |
T |
A |
18: 46,693,718 (GRCm39) |
D123V |
probably damaging |
Het |
Timm23 |
A |
G |
14: 31,920,993 (GRCm39) |
|
probably benign |
Het |
Tinag |
C |
T |
9: 76,912,969 (GRCm39) |
R280H |
probably benign |
Het |
Topbp1 |
G |
A |
9: 103,186,011 (GRCm39) |
R51K |
probably benign |
Het |
Tor1b |
A |
G |
2: 30,843,925 (GRCm39) |
I121V |
probably damaging |
Het |
Tpmt |
C |
A |
13: 47,185,930 (GRCm39) |
G148V |
probably damaging |
Het |
Tubb1 |
A |
G |
2: 174,299,548 (GRCm39) |
E410G |
probably damaging |
Het |
Ubash3b |
C |
A |
9: 40,958,360 (GRCm39) |
V7L |
possibly damaging |
Het |
Ube2o |
C |
T |
11: 116,433,661 (GRCm39) |
E686K |
probably damaging |
Het |
Unc13d |
T |
A |
11: 115,960,318 (GRCm39) |
|
probably benign |
Het |
Xkr8 |
T |
C |
4: 132,459,649 (GRCm39) |
Y43C |
probably damaging |
Het |
Zc3h4 |
T |
A |
7: 16,168,697 (GRCm39) |
N935K |
unknown |
Het |
Zc3h7a |
G |
A |
16: 10,974,167 (GRCm39) |
|
probably benign |
Het |
Zfp84 |
C |
T |
7: 29,476,276 (GRCm39) |
H323Y |
probably damaging |
Het |
Zfp873 |
G |
T |
10: 81,896,595 (GRCm39) |
S442I |
possibly damaging |
Het |
Zfp938 |
A |
G |
10: 82,061,606 (GRCm39) |
L338P |
probably damaging |
Het |
|
Other mutations in Vmn1r183 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00987:Vmn1r183
|
APN |
7 |
23,754,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01813:Vmn1r183
|
APN |
7 |
23,754,985 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03377:Vmn1r183
|
APN |
7 |
23,754,817 (GRCm39) |
missense |
possibly damaging |
0.70 |
PIT4791001:Vmn1r183
|
UTSW |
7 |
23,754,266 (GRCm39) |
missense |
probably damaging |
0.99 |
R0463:Vmn1r183
|
UTSW |
7 |
23,754,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Vmn1r183
|
UTSW |
7 |
23,754,250 (GRCm39) |
missense |
probably benign |
0.03 |
R3928:Vmn1r183
|
UTSW |
7 |
23,754,997 (GRCm39) |
missense |
probably damaging |
0.98 |
R4425:Vmn1r183
|
UTSW |
7 |
23,754,973 (GRCm39) |
missense |
probably benign |
0.00 |
R4767:Vmn1r183
|
UTSW |
7 |
23,754,531 (GRCm39) |
frame shift |
probably null |
|
R4835:Vmn1r183
|
UTSW |
7 |
23,754,564 (GRCm39) |
missense |
probably benign |
0.07 |
R5267:Vmn1r183
|
UTSW |
7 |
23,754,971 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5693:Vmn1r183
|
UTSW |
7 |
23,754,227 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6291:Vmn1r183
|
UTSW |
7 |
23,754,982 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6439:Vmn1r183
|
UTSW |
7 |
23,754,704 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7073:Vmn1r183
|
UTSW |
7 |
23,754,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R8732:Vmn1r183
|
UTSW |
7 |
23,754,890 (GRCm39) |
missense |
possibly damaging |
0.89 |
|