Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630089N07Rik |
A |
T |
16: 97,867,367 (GRCm39) |
H198Q |
probably damaging |
Het |
Abcb9 |
T |
C |
5: 124,221,706 (GRCm39) |
T223A |
probably benign |
Het |
Actc1 |
T |
A |
2: 113,880,881 (GRCm39) |
K115* |
probably null |
Het |
Angptl2 |
G |
A |
2: 33,132,316 (GRCm39) |
D308N |
probably benign |
Het |
Arl4d |
A |
C |
11: 101,557,892 (GRCm39) |
Q139H |
possibly damaging |
Het |
Aspm |
T |
A |
1: 139,418,125 (GRCm39) |
C2951* |
probably null |
Het |
Atp23 |
A |
T |
10: 126,723,362 (GRCm39) |
*247R |
probably null |
Het |
B3gnt7 |
T |
A |
1: 86,232,839 (GRCm39) |
S28R |
probably benign |
Het |
Blm |
GCCTCCTCCTCCTCCTCCTCCTCCTCCTCC |
GCCTCCTCCTCCTCCTCCTCCTCCTCC |
7: 80,162,652 (GRCm39) |
|
probably benign |
Het |
Bmp7 |
C |
T |
2: 172,721,211 (GRCm39) |
R288H |
probably damaging |
Het |
Bsdc1 |
G |
T |
4: 129,355,439 (GRCm39) |
|
probably benign |
Het |
Ccdc146 |
T |
C |
5: 21,538,060 (GRCm39) |
E88G |
probably damaging |
Het |
Ccdc73 |
C |
A |
2: 104,822,542 (GRCm39) |
D2E |
|
Het |
Cdc5l |
C |
A |
17: 45,721,839 (GRCm39) |
R477L |
|
Het |
Cdh22 |
T |
A |
2: 164,965,504 (GRCm39) |
H529L |
possibly damaging |
Het |
Chchd3 |
T |
A |
6: 32,780,951 (GRCm39) |
E178D |
probably benign |
Het |
Ciz1 |
A |
T |
2: 32,257,512 (GRCm39) |
R186* |
probably null |
Het |
Copa |
T |
A |
1: 171,931,737 (GRCm39) |
H329Q |
probably null |
Het |
Dcaf7 |
A |
G |
11: 105,942,752 (GRCm39) |
D233G |
probably damaging |
Het |
Dclk2 |
G |
T |
3: 86,739,048 (GRCm39) |
P317Q |
probably damaging |
Het |
Dsc3 |
A |
T |
18: 20,107,234 (GRCm39) |
H462Q |
probably benign |
Het |
Fn1 |
T |
C |
1: 71,638,535 (GRCm39) |
N1998S |
probably benign |
Het |
Fpr2 |
T |
C |
17: 18,113,724 (GRCm39) |
L240S |
possibly damaging |
Het |
Fzd9 |
A |
T |
5: 135,278,589 (GRCm39) |
M432K |
probably damaging |
Het |
Gm5862 |
T |
A |
5: 26,226,678 (GRCm39) |
I75F |
probably damaging |
Het |
Gpr45 |
T |
A |
1: 43,072,314 (GRCm39) |
V319D |
probably damaging |
Het |
H4c11 |
T |
C |
13: 21,919,525 (GRCm39) |
V87A |
possibly damaging |
Het |
Igfn1 |
T |
A |
1: 135,905,984 (GRCm39) |
R275W |
probably damaging |
Het |
Inafm1 |
G |
A |
7: 16,006,980 (GRCm39) |
A79V |
unknown |
Het |
Itfg1 |
C |
T |
8: 86,567,420 (GRCm39) |
|
probably benign |
Het |
Klhl35 |
T |
G |
7: 99,120,221 (GRCm39) |
I366S |
probably damaging |
Het |
Lysmd1 |
A |
T |
3: 95,045,831 (GRCm39) |
I223F |
probably damaging |
Het |
Mrps30 |
A |
G |
13: 118,523,205 (GRCm39) |
L189P |
probably damaging |
Het |
Ms4a4d |
A |
C |
19: 11,533,574 (GRCm39) |
T152P |
probably benign |
Het |
Mtcl1 |
A |
T |
17: 66,755,628 (GRCm39) |
I238K |
probably benign |
Het |
Musk |
T |
C |
4: 58,301,638 (GRCm39) |
I132T |
probably damaging |
Het |
Myh2 |
A |
T |
11: 67,079,509 (GRCm39) |
M989L |
probably benign |
Het |
Myh8 |
G |
A |
11: 67,174,081 (GRCm39) |
R172H |
probably benign |
Het |
Nt5c1a |
C |
T |
4: 123,102,281 (GRCm39) |
T69M |
possibly damaging |
Het |
Nuak2 |
T |
A |
1: 132,255,916 (GRCm39) |
D196E |
probably damaging |
Het |
Or52h7 |
A |
T |
7: 104,214,229 (GRCm39) |
H267L |
probably damaging |
Het |
Or5ap2 |
A |
T |
2: 85,679,918 (GRCm39) |
I41F |
possibly damaging |
Het |
Or5t7 |
T |
C |
2: 86,507,630 (GRCm39) |
T16A |
probably benign |
Het |
Or8k53 |
T |
C |
2: 86,178,090 (GRCm39) |
T7A |
possibly damaging |
Het |
Palb2 |
A |
T |
7: 121,723,821 (GRCm39) |
C643S |
probably damaging |
Het |
Pde5a |
T |
A |
3: 122,633,249 (GRCm39) |
I706N |
probably damaging |
Het |
Pdlim4 |
T |
C |
11: 53,950,790 (GRCm39) |
R100G |
probably benign |
Het |
Pip5k1c |
T |
A |
10: 81,128,906 (GRCm39) |
V5E |
possibly damaging |
Het |
Pira1 |
A |
C |
7: 3,742,358 (GRCm39) |
N56K |
probably benign |
Het |
Plekhm1 |
A |
G |
11: 103,268,039 (GRCm39) |
V644A |
probably benign |
Het |
Plk2 |
T |
G |
13: 110,535,750 (GRCm39) |
V524G |
probably damaging |
Het |
Ppl |
T |
A |
16: 4,905,474 (GRCm39) |
N1607I |
probably benign |
Het |
Prag1 |
T |
G |
8: 36,614,360 (GRCm39) |
V1304G |
probably damaging |
Het |
Prex1 |
C |
T |
2: 166,426,995 (GRCm39) |
V1077M |
probably damaging |
Het |
Prmt6 |
T |
C |
3: 110,158,248 (GRCm39) |
S14G |
probably benign |
Het |
Psrc1 |
T |
G |
3: 108,293,973 (GRCm39) |
S263R |
probably damaging |
Het |
Qrfprl |
C |
A |
6: 65,358,597 (GRCm39) |
S107* |
probably null |
Het |
Rbp7 |
A |
T |
4: 149,537,958 (GRCm39) |
L36* |
probably null |
Het |
Rgs12 |
G |
T |
5: 35,123,633 (GRCm39) |
W472L |
possibly damaging |
Het |
Rrp8 |
C |
A |
7: 105,384,073 (GRCm39) |
C143F |
possibly damaging |
Het |
Sart1 |
T |
C |
19: 5,438,529 (GRCm39) |
S43G |
probably benign |
Het |
Setx |
A |
G |
2: 29,016,971 (GRCm39) |
T25A |
possibly damaging |
Het |
Skint5 |
G |
A |
4: 113,341,099 (GRCm39) |
T1414I |
probably benign |
Het |
Sorbs2 |
T |
A |
8: 46,248,952 (GRCm39) |
S734R |
probably damaging |
Het |
Spata31g1 |
A |
T |
4: 42,972,251 (GRCm39) |
Y528F |
probably benign |
Het |
Spon1 |
T |
C |
7: 113,629,592 (GRCm39) |
|
probably null |
Het |
Sptbn1 |
C |
T |
11: 30,088,962 (GRCm39) |
V767I |
probably damaging |
Het |
Srf |
T |
C |
17: 46,860,095 (GRCm39) |
I477V |
probably damaging |
Het |
Tanc2 |
A |
G |
11: 105,701,331 (GRCm39) |
Y282C |
probably damaging |
Het |
Tbc1d23 |
A |
G |
16: 56,992,152 (GRCm39) |
Y603H |
probably damaging |
Het |
Tdpoz6 |
T |
A |
3: 93,599,950 (GRCm39) |
T140S |
probably benign |
Het |
Tfap4 |
T |
C |
16: 4,369,218 (GRCm39) |
D134G |
probably damaging |
Het |
Tmem200c |
A |
G |
17: 69,148,733 (GRCm39) |
T439A |
probably benign |
Het |
Tmem63b |
A |
T |
17: 45,975,908 (GRCm39) |
M515K |
probably damaging |
Het |
Tnc |
A |
T |
4: 63,925,595 (GRCm39) |
N980K |
probably damaging |
Het |
Ttc23l |
T |
A |
15: 10,530,720 (GRCm39) |
L297F |
probably damaging |
Het |
Vinac1 |
A |
G |
2: 128,882,789 (GRCm39) |
S76P |
|
Het |
Vmn1r170 |
A |
G |
7: 23,305,814 (GRCm39) |
N72S |
possibly damaging |
Het |
Vmn2r8 |
T |
C |
5: 108,950,131 (GRCm39) |
M239V |
|
Het |
Vopp1 |
A |
G |
6: 57,731,578 (GRCm39) |
F138L |
probably damaging |
Het |
Zfp317 |
T |
C |
9: 19,552,521 (GRCm39) |
M1T |
probably null |
Het |
|
Other mutations in Vps41 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01134:Vps41
|
APN |
13 |
19,050,320 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01563:Vps41
|
APN |
13 |
18,966,897 (GRCm39) |
splice site |
probably benign |
|
IGL01880:Vps41
|
APN |
13 |
18,994,641 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02024:Vps41
|
APN |
13 |
18,975,827 (GRCm39) |
splice site |
probably benign |
|
IGL02458:Vps41
|
APN |
13 |
19,037,649 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02740:Vps41
|
APN |
13 |
19,022,850 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03218:Vps41
|
APN |
13 |
19,013,440 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0197:Vps41
|
UTSW |
13 |
19,038,833 (GRCm39) |
critical splice donor site |
probably null |
|
R0284:Vps41
|
UTSW |
13 |
19,037,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R0321:Vps41
|
UTSW |
13 |
19,026,465 (GRCm39) |
splice site |
probably benign |
|
R0372:Vps41
|
UTSW |
13 |
19,026,417 (GRCm39) |
missense |
probably benign |
0.00 |
R0382:Vps41
|
UTSW |
13 |
19,011,897 (GRCm39) |
missense |
probably benign |
0.30 |
R1691:Vps41
|
UTSW |
13 |
19,025,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R2055:Vps41
|
UTSW |
13 |
19,038,786 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2082:Vps41
|
UTSW |
13 |
19,036,521 (GRCm39) |
missense |
probably benign |
0.27 |
R2147:Vps41
|
UTSW |
13 |
19,023,904 (GRCm39) |
splice site |
probably null |
|
R2897:Vps41
|
UTSW |
13 |
18,994,598 (GRCm39) |
splice site |
probably benign |
|
R4322:Vps41
|
UTSW |
13 |
19,007,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Vps41
|
UTSW |
13 |
18,929,453 (GRCm39) |
missense |
probably damaging |
0.97 |
R4751:Vps41
|
UTSW |
13 |
18,995,792 (GRCm39) |
missense |
probably damaging |
0.98 |
R4856:Vps41
|
UTSW |
13 |
19,013,425 (GRCm39) |
missense |
probably damaging |
0.98 |
R5389:Vps41
|
UTSW |
13 |
19,046,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R7022:Vps41
|
UTSW |
13 |
19,026,438 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7456:Vps41
|
UTSW |
13 |
19,048,204 (GRCm39) |
missense |
probably benign |
0.02 |
R7747:Vps41
|
UTSW |
13 |
19,025,422 (GRCm39) |
critical splice donor site |
probably null |
|
R7790:Vps41
|
UTSW |
13 |
19,026,438 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8029:Vps41
|
UTSW |
13 |
19,007,955 (GRCm39) |
nonsense |
probably null |
|
R8033:Vps41
|
UTSW |
13 |
18,994,635 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8241:Vps41
|
UTSW |
13 |
19,033,168 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8267:Vps41
|
UTSW |
13 |
18,994,641 (GRCm39) |
missense |
probably benign |
0.00 |
R8801:Vps41
|
UTSW |
13 |
18,998,403 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8927:Vps41
|
UTSW |
13 |
18,929,501 (GRCm39) |
missense |
probably benign |
0.01 |
R9029:Vps41
|
UTSW |
13 |
18,994,723 (GRCm39) |
critical splice donor site |
probably null |
|
R9057:Vps41
|
UTSW |
13 |
19,027,702 (GRCm39) |
missense |
probably benign |
0.19 |
R9066:Vps41
|
UTSW |
13 |
19,008,018 (GRCm39) |
missense |
probably damaging |
0.99 |
R9113:Vps41
|
UTSW |
13 |
19,023,883 (GRCm39) |
missense |
probably benign |
0.25 |
R9129:Vps41
|
UTSW |
13 |
19,011,775 (GRCm39) |
missense |
probably benign |
0.00 |
R9282:Vps41
|
UTSW |
13 |
19,013,401 (GRCm39) |
nonsense |
probably null |
|
R9391:Vps41
|
UTSW |
13 |
18,994,616 (GRCm39) |
missense |
probably benign |
0.19 |
R9478:Vps41
|
UTSW |
13 |
19,046,913 (GRCm39) |
missense |
|
|
R9569:Vps41
|
UTSW |
13 |
19,013,396 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Vps41
|
UTSW |
13 |
19,038,765 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Vps41
|
UTSW |
13 |
19,030,105 (GRCm39) |
missense |
probably benign |
0.00 |
|