Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610318N02Rik |
T |
A |
16: 16,935,446 (GRCm39) |
H214L |
probably benign |
Het |
Abca17 |
T |
C |
17: 24,508,325 (GRCm39) |
E1070G |
possibly damaging |
Het |
Accsl |
A |
T |
2: 93,696,589 (GRCm39) |
|
probably benign |
Het |
Akp3 |
G |
A |
1: 87,055,593 (GRCm39) |
G547R |
unknown |
Het |
Anapc1 |
C |
A |
2: 128,522,108 (GRCm39) |
C150F |
probably damaging |
Het |
Aoc1l3 |
C |
A |
6: 48,967,173 (GRCm39) |
P707H |
probably damaging |
Het |
Arhgef18 |
T |
A |
8: 3,439,023 (GRCm39) |
|
probably benign |
Het |
Borcs5 |
T |
A |
6: 134,687,096 (GRCm39) |
N150K |
probably damaging |
Het |
C9orf72 |
C |
A |
4: 35,218,630 (GRCm39) |
E76D |
probably damaging |
Het |
Cdh20 |
G |
A |
1: 109,988,862 (GRCm39) |
V255I |
probably benign |
Het |
Cntnap5c |
C |
A |
17: 58,671,241 (GRCm39) |
T1143K |
possibly damaging |
Het |
Col7a1 |
A |
C |
9: 108,784,402 (GRCm39) |
T137P |
unknown |
Het |
Defb8 |
C |
T |
8: 19,495,910 (GRCm39) |
G50E |
probably damaging |
Het |
Dimt1 |
T |
A |
13: 107,086,193 (GRCm39) |
|
probably benign |
Het |
Dnajb11 |
T |
A |
16: 22,689,423 (GRCm39) |
D281E |
probably damaging |
Het |
Eci2 |
G |
T |
13: 35,177,087 (GRCm39) |
N24K |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,236,607 (GRCm39) |
C358S |
probably benign |
Het |
Fbxl13 |
A |
T |
5: 21,825,602 (GRCm39) |
|
probably benign |
Het |
Fbxw11 |
T |
C |
11: 32,661,922 (GRCm39) |
C121R |
probably damaging |
Het |
Fsd2 |
T |
C |
7: 81,209,518 (GRCm39) |
D108G |
probably benign |
Het |
Gab1 |
C |
A |
8: 81,511,471 (GRCm39) |
R458L |
probably damaging |
Het |
Ghrhr |
T |
A |
6: 55,365,254 (GRCm39) |
L416* |
probably null |
Het |
Glipr1l2 |
C |
A |
10: 111,919,371 (GRCm39) |
L31I |
possibly damaging |
Het |
Gm1818 |
A |
G |
12: 48,602,982 (GRCm39) |
|
noncoding transcript |
Het |
Gm19965 |
T |
A |
1: 116,748,550 (GRCm39) |
|
probably benign |
Het |
Gpr149 |
A |
G |
3: 62,511,888 (GRCm39) |
L37P |
probably damaging |
Het |
Hoxa9 |
A |
G |
6: 52,202,693 (GRCm39) |
I131T |
probably damaging |
Het |
Itpkc |
T |
C |
7: 26,927,195 (GRCm39) |
I240V |
probably benign |
Het |
Jakmip3 |
A |
G |
7: 138,629,515 (GRCm39) |
D552G |
probably damaging |
Het |
Kank4 |
T |
C |
4: 98,653,806 (GRCm39) |
Y874C |
probably damaging |
Het |
Kdm3a |
T |
C |
6: 71,577,011 (GRCm39) |
E768G |
possibly damaging |
Het |
Klf6 |
A |
G |
13: 5,911,711 (GRCm39) |
D25G |
probably benign |
Het |
Lamc1 |
T |
C |
1: 153,122,977 (GRCm39) |
|
probably benign |
Het |
Laptm4a |
T |
C |
12: 8,986,716 (GRCm39) |
V258A |
probably damaging |
Het |
Map3k19 |
A |
G |
1: 127,751,617 (GRCm39) |
V578A |
probably benign |
Het |
Mast1 |
T |
C |
8: 85,651,956 (GRCm39) |
E342G |
probably benign |
Het |
Mgat5b |
T |
C |
11: 116,868,622 (GRCm39) |
L515P |
probably damaging |
Het |
Mink1 |
A |
G |
11: 70,502,166 (GRCm39) |
D985G |
probably benign |
Het |
Mphosph9 |
A |
G |
5: 124,453,739 (GRCm39) |
V191A |
possibly damaging |
Het |
Muc6 |
C |
T |
7: 141,234,368 (GRCm39) |
G708S |
probably damaging |
Het |
Pcnt |
A |
T |
10: 76,228,878 (GRCm39) |
|
probably null |
Het |
Psmd8 |
A |
T |
7: 28,875,598 (GRCm39) |
Y174N |
probably damaging |
Het |
Ptgdr2 |
C |
A |
19: 10,918,292 (GRCm39) |
R270S |
possibly damaging |
Het |
Rasal2 |
A |
G |
1: 156,975,218 (GRCm39) |
M1172T |
probably damaging |
Het |
Rif1 |
A |
G |
2: 51,997,640 (GRCm39) |
|
probably benign |
Het |
Rnf123 |
C |
T |
9: 107,954,572 (GRCm39) |
R48H |
probably benign |
Het |
Rsrc1 |
T |
C |
3: 67,263,551 (GRCm39) |
|
probably benign |
Het |
Rxfp2 |
T |
C |
5: 149,975,021 (GRCm39) |
V210A |
probably benign |
Het |
Serpinb9d |
C |
T |
13: 33,384,608 (GRCm39) |
P195L |
probably benign |
Het |
Sis |
A |
G |
3: 72,865,437 (GRCm39) |
|
probably benign |
Het |
Skint4 |
T |
C |
4: 111,981,793 (GRCm39) |
M246T |
probably benign |
Het |
Snrnp200 |
C |
A |
2: 127,070,997 (GRCm39) |
R1093S |
probably damaging |
Het |
Sp100 |
A |
G |
1: 85,629,141 (GRCm39) |
N471D |
possibly damaging |
Het |
Spmip4 |
T |
A |
6: 50,566,121 (GRCm39) |
K118M |
probably damaging |
Het |
Ssxb8 |
T |
G |
X: 8,556,062 (GRCm39) |
H88P |
probably damaging |
Het |
Sufu |
T |
C |
19: 46,389,703 (GRCm39) |
|
probably null |
Het |
Synpo2l |
G |
A |
14: 20,718,235 (GRCm39) |
T10I |
possibly damaging |
Het |
Tdo2 |
A |
T |
3: 81,881,683 (GRCm39) |
S40R |
probably damaging |
Het |
Tent4b |
T |
A |
8: 88,978,635 (GRCm39) |
F445L |
probably damaging |
Het |
Terb1 |
G |
A |
8: 105,210,938 (GRCm39) |
T363I |
probably benign |
Het |
Timd4 |
C |
T |
11: 46,708,498 (GRCm39) |
P175S |
probably damaging |
Het |
Tlr3 |
C |
A |
8: 45,850,171 (GRCm39) |
V833L |
probably damaging |
Het |
Tpst2 |
T |
A |
5: 112,455,911 (GRCm39) |
M150K |
probably damaging |
Het |
Trim67 |
T |
A |
8: 125,543,774 (GRCm39) |
V378E |
probably damaging |
Het |
Tyrp1 |
C |
T |
4: 80,763,105 (GRCm39) |
Q331* |
probably null |
Het |
Ubap2l |
A |
T |
3: 89,930,807 (GRCm39) |
S413T |
probably benign |
Het |
Uimc1 |
G |
A |
13: 55,176,415 (GRCm39) |
T701I |
possibly damaging |
Het |
Vangl2 |
G |
T |
1: 171,832,353 (GRCm39) |
T501N |
probably damaging |
Het |
Vmn2r66 |
G |
T |
7: 84,654,799 (GRCm39) |
D503E |
probably benign |
Het |
Vmn2r72 |
T |
A |
7: 85,401,152 (GRCm39) |
E89V |
probably damaging |
Het |
Zfp457 |
G |
A |
13: 67,441,748 (GRCm39) |
P180S |
probably damaging |
Het |
|
Other mutations in Vmn1r60 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01869:Vmn1r60
|
APN |
7 |
5,547,228 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01892:Vmn1r60
|
APN |
7 |
5,547,309 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02427:Vmn1r60
|
APN |
7 |
5,547,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03071:Vmn1r60
|
APN |
7 |
5,547,368 (GRCm39) |
missense |
probably damaging |
0.97 |
R0200:Vmn1r60
|
UTSW |
7 |
5,547,379 (GRCm39) |
missense |
probably benign |
|
R0457:Vmn1r60
|
UTSW |
7 |
5,548,118 (GRCm39) |
start gained |
probably benign |
|
R1199:Vmn1r60
|
UTSW |
7 |
5,547,971 (GRCm39) |
missense |
probably damaging |
0.99 |
R1529:Vmn1r60
|
UTSW |
7 |
5,547,902 (GRCm39) |
missense |
probably benign |
0.00 |
R1859:Vmn1r60
|
UTSW |
7 |
5,547,549 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2033:Vmn1r60
|
UTSW |
7 |
5,547,819 (GRCm39) |
missense |
probably benign |
|
R2405:Vmn1r60
|
UTSW |
7 |
5,547,912 (GRCm39) |
missense |
probably benign |
|
R3408:Vmn1r60
|
UTSW |
7 |
5,548,148 (GRCm39) |
splice site |
probably null |
|
R3771:Vmn1r60
|
UTSW |
7 |
5,547,710 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3773:Vmn1r60
|
UTSW |
7 |
5,547,710 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3852:Vmn1r60
|
UTSW |
7 |
5,548,026 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4236:Vmn1r60
|
UTSW |
7 |
5,547,803 (GRCm39) |
missense |
probably benign |
0.06 |
R4331:Vmn1r60
|
UTSW |
7 |
5,547,364 (GRCm39) |
nonsense |
probably null |
|
R4439:Vmn1r60
|
UTSW |
7 |
5,547,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R5099:Vmn1r60
|
UTSW |
7 |
5,547,816 (GRCm39) |
missense |
probably damaging |
0.98 |
R5325:Vmn1r60
|
UTSW |
7 |
5,547,201 (GRCm39) |
missense |
probably benign |
|
R5415:Vmn1r60
|
UTSW |
7 |
5,547,416 (GRCm39) |
missense |
probably benign |
0.38 |
R5818:Vmn1r60
|
UTSW |
7 |
5,548,098 (GRCm39) |
start codon destroyed |
probably benign |
0.04 |
R6375:Vmn1r60
|
UTSW |
7 |
5,548,017 (GRCm39) |
missense |
probably damaging |
0.96 |
R6378:Vmn1r60
|
UTSW |
7 |
5,547,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R6478:Vmn1r60
|
UTSW |
7 |
5,547,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R6572:Vmn1r60
|
UTSW |
7 |
5,547,599 (GRCm39) |
missense |
probably benign |
0.40 |
R6586:Vmn1r60
|
UTSW |
7 |
5,547,446 (GRCm39) |
missense |
probably benign |
0.00 |
R7061:Vmn1r60
|
UTSW |
7 |
5,547,310 (GRCm39) |
nonsense |
probably null |
|
R7506:Vmn1r60
|
UTSW |
7 |
5,547,861 (GRCm39) |
missense |
|
|
R7589:Vmn1r60
|
UTSW |
7 |
5,547,688 (GRCm39) |
missense |
|
|
R8182:Vmn1r60
|
UTSW |
7 |
5,547,876 (GRCm39) |
missense |
|
|
R9295:Vmn1r60
|
UTSW |
7 |
5,547,218 (GRCm39) |
missense |
probably null |
|
R9408:Vmn1r60
|
UTSW |
7 |
5,547,918 (GRCm39) |
missense |
|
|
|