Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
A |
G |
7: 41,275,262 (GRCm39) |
T322A |
probably benign |
Het |
Abhd13 |
C |
T |
8: 10,038,071 (GRCm39) |
P223S |
possibly damaging |
Het |
Adgra3 |
T |
A |
5: 50,117,905 (GRCm39) |
L1214F |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Ankrd13a |
C |
A |
5: 114,927,373 (GRCm39) |
P120Q |
probably damaging |
Het |
Apbb1ip |
A |
G |
2: 22,739,556 (GRCm39) |
Y277C |
probably damaging |
Het |
Arfgap1 |
T |
C |
2: 180,618,166 (GRCm39) |
|
probably benign |
Het |
Arid2 |
T |
A |
15: 96,290,343 (GRCm39) |
V1746D |
probably damaging |
Het |
C1qtnf7 |
T |
A |
5: 43,766,549 (GRCm39) |
N49K |
possibly damaging |
Het |
Cacnb2 |
A |
T |
2: 14,990,811 (GRCm39) |
D587V |
possibly damaging |
Het |
Ccar2 |
A |
T |
14: 70,389,359 (GRCm39) |
|
probably null |
Het |
Cdk2ap2 |
T |
C |
19: 4,147,879 (GRCm39) |
F49L |
possibly damaging |
Het |
Cdon |
A |
T |
9: 35,388,265 (GRCm39) |
I747F |
probably damaging |
Het |
Cyp19a1 |
G |
A |
9: 54,100,607 (GRCm39) |
P27S |
probably benign |
Het |
Cyp4v3 |
T |
A |
8: 45,760,029 (GRCm39) |
R508W |
probably damaging |
Het |
Dclk1 |
T |
C |
3: 55,154,831 (GRCm39) |
L87P |
probably damaging |
Het |
Ddx41 |
G |
A |
13: 55,683,834 (GRCm39) |
R66C |
possibly damaging |
Het |
Dmxl1 |
T |
C |
18: 49,985,427 (GRCm39) |
Y225H |
probably damaging |
Het |
Dnah7a |
G |
A |
1: 53,450,818 (GRCm39) |
P3871S |
probably benign |
Het |
Dnhd1 |
A |
G |
7: 105,306,373 (GRCm39) |
|
probably null |
Het |
Dph1 |
A |
T |
11: 75,069,721 (GRCm39) |
|
probably benign |
Het |
Egln2 |
A |
G |
7: 26,859,008 (GRCm39) |
I382T |
probably damaging |
Het |
Enpp3 |
A |
G |
10: 24,652,780 (GRCm39) |
Y726H |
probably damaging |
Het |
Fbxo32 |
A |
G |
15: 58,044,873 (GRCm39) |
F353L |
probably damaging |
Het |
Fchsd2 |
G |
A |
7: 100,926,809 (GRCm39) |
G657D |
possibly damaging |
Het |
Fer1l4 |
T |
A |
2: 155,878,559 (GRCm39) |
E44V |
possibly damaging |
Het |
Gjb2 |
C |
T |
14: 57,337,762 (GRCm39) |
V149I |
probably benign |
Het |
Glipr1l1 |
A |
G |
10: 111,898,317 (GRCm39) |
M141V |
probably benign |
Het |
Gnaq |
T |
C |
19: 16,312,370 (GRCm39) |
S211P |
probably damaging |
Het |
Gnl1 |
A |
G |
17: 36,299,142 (GRCm39) |
R527G |
probably benign |
Het |
Gns |
A |
G |
10: 121,217,083 (GRCm39) |
Q286R |
probably benign |
Het |
Gon4l |
T |
C |
3: 88,817,397 (GRCm39) |
|
probably benign |
Het |
Gpr107 |
T |
C |
2: 31,097,677 (GRCm39) |
|
probably benign |
Het |
Gprasp1 |
C |
T |
X: 134,703,592 (GRCm39) |
R1262C |
probably damaging |
Het |
Gtf2ird1 |
A |
T |
5: 134,439,857 (GRCm39) |
D124E |
probably damaging |
Het |
Hbp1 |
T |
A |
12: 32,000,231 (GRCm39) |
|
probably benign |
Het |
Hrnr |
C |
T |
3: 93,230,875 (GRCm39) |
T371I |
unknown |
Het |
Ints2 |
A |
G |
11: 86,147,024 (GRCm39) |
C41R |
probably damaging |
Het |
Jhy |
A |
G |
9: 40,822,389 (GRCm39) |
I583T |
probably benign |
Het |
Jph4 |
G |
T |
14: 55,352,503 (GRCm39) |
R77S |
probably damaging |
Het |
Kcnd3 |
C |
T |
3: 105,566,082 (GRCm39) |
A421V |
probably damaging |
Het |
Klhl12 |
A |
T |
1: 134,413,507 (GRCm39) |
I331F |
probably benign |
Het |
Map4k4 |
G |
A |
1: 40,039,698 (GRCm39) |
R30Q |
probably damaging |
Het |
Mgst1 |
C |
A |
6: 138,133,213 (GRCm39) |
T176K |
probably damaging |
Het |
Negr1 |
C |
A |
3: 156,914,013 (GRCm39) |
|
probably benign |
Het |
Nrg1 |
C |
T |
8: 32,407,802 (GRCm39) |
V144I |
probably benign |
Het |
Ntmt2 |
T |
A |
1: 163,530,586 (GRCm39) |
*284C |
probably null |
Het |
Or1ad8 |
T |
C |
11: 50,898,381 (GRCm39) |
I194T |
possibly damaging |
Het |
Otog |
A |
G |
7: 45,959,571 (GRCm39) |
D720G |
probably damaging |
Het |
Pex11b |
A |
T |
3: 96,551,330 (GRCm39) |
|
probably benign |
Het |
Phtf2 |
T |
C |
5: 20,994,593 (GRCm39) |
|
probably benign |
Het |
Ppip5k1 |
C |
T |
2: 121,174,044 (GRCm39) |
R359Q |
possibly damaging |
Het |
Prickle2 |
T |
C |
6: 92,399,323 (GRCm39) |
I185V |
probably benign |
Het |
Prrc2a |
G |
A |
17: 35,377,473 (GRCm39) |
P562S |
unknown |
Het |
Rdx |
A |
G |
9: 51,980,141 (GRCm39) |
I245V |
probably benign |
Het |
Rem2 |
T |
C |
14: 54,715,116 (GRCm39) |
S98P |
probably damaging |
Het |
Rhob |
T |
G |
12: 8,549,373 (GRCm39) |
D87A |
probably damaging |
Het |
Ros1 |
T |
A |
10: 52,040,090 (GRCm39) |
E300D |
probably damaging |
Het |
Sbf2 |
A |
G |
7: 109,948,060 (GRCm39) |
|
probably null |
Het |
Sipa1l3 |
G |
T |
7: 29,025,287 (GRCm39) |
P619Q |
probably damaging |
Het |
Snupn |
A |
G |
9: 56,885,346 (GRCm39) |
E217G |
probably benign |
Het |
Ston2 |
T |
A |
12: 91,606,496 (GRCm39) |
*896C |
probably null |
Het |
Stradb |
C |
T |
1: 59,019,117 (GRCm39) |
R13* |
probably null |
Het |
Tbx21 |
G |
A |
11: 97,005,581 (GRCm39) |
A128V |
probably benign |
Het |
Tep1 |
A |
T |
14: 51,062,197 (GRCm39) |
C2552S |
probably benign |
Het |
Tgif1 |
A |
T |
17: 71,151,912 (GRCm39) |
V233E |
possibly damaging |
Het |
Trim31 |
A |
T |
17: 37,209,633 (GRCm39) |
I130L |
probably benign |
Het |
Trrap |
C |
T |
5: 144,728,928 (GRCm39) |
T614I |
probably benign |
Het |
Ttn |
C |
A |
2: 76,766,758 (GRCm39) |
V3107F |
probably damaging |
Het |
Txnrd2 |
T |
G |
16: 18,274,956 (GRCm39) |
D322E |
probably benign |
Het |
Unc45b |
T |
A |
11: 82,827,315 (GRCm39) |
|
probably null |
Het |
Usp43 |
C |
T |
11: 67,789,788 (GRCm39) |
C252Y |
probably damaging |
Het |
Usp43 |
A |
T |
11: 67,766,178 (GRCm39) |
L744* |
probably null |
Het |
Vmn2r71 |
A |
C |
7: 85,273,402 (GRCm39) |
K739Q |
possibly damaging |
Het |
Wdr83os |
T |
A |
8: 85,808,495 (GRCm39) |
S82R |
probably damaging |
Het |
Xpo6 |
T |
A |
7: 125,727,427 (GRCm39) |
L526F |
probably damaging |
Het |
Zfhx4 |
G |
A |
3: 5,466,894 (GRCm39) |
V2351I |
probably benign |
Het |
Zfp558 |
A |
T |
9: 18,367,799 (GRCm39) |
C330S |
possibly damaging |
Het |
|
Other mutations in Vps16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01327:Vps16
|
APN |
2 |
130,279,616 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01400:Vps16
|
APN |
2 |
130,280,273 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01542:Vps16
|
APN |
2 |
130,280,314 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02011:Vps16
|
APN |
2 |
130,283,399 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02192:Vps16
|
APN |
2 |
130,282,852 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02220:Vps16
|
APN |
2 |
130,283,573 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02587:Vps16
|
APN |
2 |
130,281,636 (GRCm39) |
critical splice donor site |
probably null |
|
R0427:Vps16
|
UTSW |
2 |
130,280,770 (GRCm39) |
missense |
probably benign |
0.00 |
R0507:Vps16
|
UTSW |
2 |
130,279,632 (GRCm39) |
critical splice donor site |
probably null |
|
R1550:Vps16
|
UTSW |
2 |
130,282,260 (GRCm39) |
missense |
probably benign |
0.09 |
R1789:Vps16
|
UTSW |
2 |
130,285,520 (GRCm39) |
missense |
probably benign |
0.42 |
R3895:Vps16
|
UTSW |
2 |
130,280,596 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3981:Vps16
|
UTSW |
2 |
130,284,514 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4092:Vps16
|
UTSW |
2 |
130,281,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R4555:Vps16
|
UTSW |
2 |
130,285,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4803:Vps16
|
UTSW |
2 |
130,280,030 (GRCm39) |
missense |
probably benign |
0.27 |
R4835:Vps16
|
UTSW |
2 |
130,280,220 (GRCm39) |
splice site |
probably benign |
|
R5022:Vps16
|
UTSW |
2 |
130,281,372 (GRCm39) |
missense |
probably benign |
0.07 |
R5023:Vps16
|
UTSW |
2 |
130,281,372 (GRCm39) |
missense |
probably benign |
0.07 |
R5057:Vps16
|
UTSW |
2 |
130,281,372 (GRCm39) |
missense |
probably benign |
0.07 |
R5158:Vps16
|
UTSW |
2 |
130,283,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R5177:Vps16
|
UTSW |
2 |
130,285,288 (GRCm39) |
nonsense |
probably null |
|
R5540:Vps16
|
UTSW |
2 |
130,284,305 (GRCm39) |
missense |
probably benign |
0.00 |
R5680:Vps16
|
UTSW |
2 |
130,282,244 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5689:Vps16
|
UTSW |
2 |
130,281,011 (GRCm39) |
nonsense |
probably null |
|
R5690:Vps16
|
UTSW |
2 |
130,281,011 (GRCm39) |
nonsense |
probably null |
|
R5926:Vps16
|
UTSW |
2 |
130,285,476 (GRCm39) |
missense |
probably damaging |
0.97 |
R5992:Vps16
|
UTSW |
2 |
130,266,369 (GRCm39) |
critical splice donor site |
probably null |
|
R6135:Vps16
|
UTSW |
2 |
130,280,573 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6370:Vps16
|
UTSW |
2 |
130,285,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R6898:Vps16
|
UTSW |
2 |
130,279,601 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7378:Vps16
|
UTSW |
2 |
130,280,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R7487:Vps16
|
UTSW |
2 |
130,280,977 (GRCm39) |
nonsense |
probably null |
|
R7641:Vps16
|
UTSW |
2 |
130,282,448 (GRCm39) |
missense |
probably benign |
0.28 |
R7720:Vps16
|
UTSW |
2 |
130,283,623 (GRCm39) |
nonsense |
probably null |
|
R8246:Vps16
|
UTSW |
2 |
130,280,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R8363:Vps16
|
UTSW |
2 |
130,284,161 (GRCm39) |
missense |
probably benign |
0.08 |
R9092:Vps16
|
UTSW |
2 |
130,281,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R9128:Vps16
|
UTSW |
2 |
130,266,319 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9352:Vps16
|
UTSW |
2 |
130,283,823 (GRCm39) |
critical splice donor site |
probably null |
|
R9406:Vps16
|
UTSW |
2 |
130,283,425 (GRCm39) |
critical splice donor site |
probably null |
|
R9508:Vps16
|
UTSW |
2 |
130,284,361 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9800:Vps16
|
UTSW |
2 |
130,282,405 (GRCm39) |
missense |
probably benign |
0.02 |
RF021:Vps16
|
UTSW |
2 |
130,280,129 (GRCm39) |
missense |
probably benign |
0.09 |
Z1177:Vps16
|
UTSW |
2 |
130,283,346 (GRCm39) |
missense |
probably damaging |
1.00 |
|