Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ano5 |
A |
C |
7: 51,224,525 (GRCm39) |
S480R |
probably benign |
Het |
Aqr |
A |
G |
2: 114,005,646 (GRCm39) |
M1T |
probably null |
Het |
Arhgef28 |
A |
G |
13: 98,211,530 (GRCm39) |
V151A |
possibly damaging |
Het |
Atp6v1b2 |
T |
A |
8: 69,555,148 (GRCm39) |
I170N |
probably damaging |
Het |
Atxn2 |
T |
A |
5: 121,949,055 (GRCm39) |
V817D |
probably damaging |
Het |
Cdh23 |
A |
C |
10: 60,143,761 (GRCm39) |
I2950S |
probably damaging |
Het |
Ces1h |
A |
G |
8: 94,083,691 (GRCm39) |
L417P |
unknown |
Het |
Cimap3 |
T |
C |
3: 105,906,937 (GRCm39) |
D154G |
possibly damaging |
Het |
Csf1r |
A |
G |
18: 61,242,784 (GRCm39) |
E49G |
possibly damaging |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Fat3 |
A |
G |
9: 16,287,346 (GRCm39) |
S726P |
possibly damaging |
Het |
Grik2 |
A |
T |
10: 49,399,959 (GRCm39) |
|
probably null |
Het |
Il9r |
A |
G |
11: 32,142,674 (GRCm39) |
V287A |
probably benign |
Het |
Inpp5b |
T |
C |
4: 124,692,143 (GRCm39) |
C909R |
possibly damaging |
Het |
Kat7 |
G |
A |
11: 95,174,860 (GRCm39) |
H384Y |
probably damaging |
Het |
Lama5 |
A |
G |
2: 179,827,185 (GRCm39) |
S2272P |
probably benign |
Het |
Megf10 |
A |
G |
18: 57,386,100 (GRCm39) |
H371R |
probably benign |
Het |
Moxd2 |
A |
T |
6: 40,860,688 (GRCm39) |
Y310N |
probably damaging |
Het |
Ntrk2 |
A |
T |
13: 59,208,209 (GRCm39) |
E685V |
probably damaging |
Het |
Ogfr |
G |
T |
2: 180,236,467 (GRCm39) |
G351W |
probably damaging |
Het |
Or52ac1 |
G |
T |
7: 104,245,915 (GRCm39) |
P158T |
probably damaging |
Het |
Parp3 |
C |
T |
9: 106,351,481 (GRCm39) |
V207M |
possibly damaging |
Het |
Pfkfb3 |
T |
C |
2: 11,486,146 (GRCm39) |
|
probably null |
Het |
Pigr |
T |
C |
1: 130,774,998 (GRCm39) |
V475A |
probably benign |
Het |
Pik3ap1 |
T |
A |
19: 41,316,640 (GRCm39) |
Y250F |
probably benign |
Het |
Ppp1r3c |
A |
T |
19: 36,711,206 (GRCm39) |
I188N |
probably damaging |
Het |
Prmt7 |
T |
G |
8: 106,961,640 (GRCm39) |
|
probably benign |
Het |
Psapl1 |
T |
C |
5: 36,361,594 (GRCm39) |
V62A |
probably benign |
Het |
Relch |
T |
C |
1: 105,619,683 (GRCm39) |
L280S |
probably damaging |
Het |
Rpp14 |
G |
A |
14: 8,090,462 (GRCm38) |
V129I |
probably benign |
Het |
Sema4f |
A |
G |
6: 82,916,553 (GRCm39) |
|
probably benign |
Het |
Serpinb13 |
C |
A |
1: 106,928,337 (GRCm39) |
A319E |
probably benign |
Het |
Sez6l2 |
A |
T |
7: 126,552,625 (GRCm39) |
S134C |
probably damaging |
Het |
Slc4a10 |
T |
A |
2: 62,059,046 (GRCm39) |
H184Q |
probably benign |
Het |
Slc9a9 |
G |
T |
9: 94,821,602 (GRCm39) |
A330S |
probably benign |
Het |
Sord |
T |
C |
2: 122,087,424 (GRCm39) |
V176A |
probably damaging |
Het |
Ssbp2 |
G |
T |
13: 91,817,862 (GRCm39) |
|
probably null |
Het |
Stab2 |
G |
T |
10: 86,773,906 (GRCm39) |
N808K |
probably damaging |
Het |
Syne1 |
A |
G |
10: 5,296,819 (GRCm39) |
|
probably null |
Het |
Tpcn2 |
A |
G |
7: 144,820,588 (GRCm39) |
V341A |
probably damaging |
Het |
Unc13b |
C |
A |
4: 43,177,995 (GRCm39) |
S2941* |
probably null |
Het |
Utrn |
T |
A |
10: 12,354,168 (GRCm39) |
H2806L |
possibly damaging |
Het |
Vmn1r40 |
C |
A |
6: 89,691,588 (GRCm39) |
A135D |
probably damaging |
Het |
Wiz |
T |
A |
17: 32,606,574 (GRCm39) |
I54F |
probably damaging |
Het |
|
Other mutations in Vmn1r68 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01892:Vmn1r68
|
APN |
7 |
10,261,334 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02051:Vmn1r68
|
APN |
7 |
10,261,948 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02112:Vmn1r68
|
APN |
7 |
10,261,787 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02619:Vmn1r68
|
APN |
7 |
10,261,603 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03033:Vmn1r68
|
APN |
7 |
10,262,074 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03184:Vmn1r68
|
APN |
7 |
10,261,799 (GRCm39) |
missense |
probably benign |
0.16 |
PIT4354001:Vmn1r68
|
UTSW |
7 |
10,261,958 (GRCm39) |
missense |
probably benign |
|
R0141:Vmn1r68
|
UTSW |
7 |
10,261,252 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0359:Vmn1r68
|
UTSW |
7 |
10,261,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R0634:Vmn1r68
|
UTSW |
7 |
10,261,162 (GRCm39) |
missense |
probably benign |
0.00 |
R1731:Vmn1r68
|
UTSW |
7 |
10,261,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R2021:Vmn1r68
|
UTSW |
7 |
10,261,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R2022:Vmn1r68
|
UTSW |
7 |
10,261,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R2243:Vmn1r68
|
UTSW |
7 |
10,262,089 (GRCm39) |
missense |
probably damaging |
0.98 |
R2262:Vmn1r68
|
UTSW |
7 |
10,261,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R3877:Vmn1r68
|
UTSW |
7 |
10,261,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Vmn1r68
|
UTSW |
7 |
10,261,275 (GRCm39) |
missense |
probably benign |
0.23 |
R4843:Vmn1r68
|
UTSW |
7 |
10,261,904 (GRCm39) |
missense |
probably benign |
0.00 |
R5198:Vmn1r68
|
UTSW |
7 |
10,261,723 (GRCm39) |
missense |
probably benign |
0.00 |
R5835:Vmn1r68
|
UTSW |
7 |
10,261,747 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5906:Vmn1r68
|
UTSW |
7 |
10,261,550 (GRCm39) |
missense |
probably benign |
0.02 |
R7073:Vmn1r68
|
UTSW |
7 |
10,261,778 (GRCm39) |
missense |
probably benign |
0.00 |
R7614:Vmn1r68
|
UTSW |
7 |
10,261,553 (GRCm39) |
missense |
probably benign |
0.05 |
R7699:Vmn1r68
|
UTSW |
7 |
10,261,559 (GRCm39) |
missense |
probably benign |
0.15 |
R7700:Vmn1r68
|
UTSW |
7 |
10,261,559 (GRCm39) |
missense |
probably benign |
0.15 |
R7912:Vmn1r68
|
UTSW |
7 |
10,261,237 (GRCm39) |
missense |
probably benign |
0.01 |
R8166:Vmn1r68
|
UTSW |
7 |
10,261,888 (GRCm39) |
missense |
probably benign |
0.10 |
R8426:Vmn1r68
|
UTSW |
7 |
10,261,382 (GRCm39) |
missense |
probably benign |
0.02 |
R9466:Vmn1r68
|
UTSW |
7 |
10,261,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R9466:Vmn1r68
|
UTSW |
7 |
10,261,317 (GRCm39) |
nonsense |
probably null |
|
|