Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930544G11Rik |
A |
T |
6: 65,930,289 (GRCm39) |
T175S |
probably benign |
Het |
Abca13 |
A |
G |
11: 9,531,590 (GRCm39) |
I4606V |
probably damaging |
Het |
Abca3 |
G |
A |
17: 24,604,827 (GRCm39) |
V645I |
probably benign |
Het |
Abi3bp |
A |
T |
16: 56,498,105 (GRCm39) |
R980* |
probably null |
Het |
Acsl6 |
G |
T |
11: 54,236,797 (GRCm39) |
G564* |
probably null |
Het |
Alppl2 |
T |
C |
1: 87,015,159 (GRCm39) |
E430G |
probably benign |
Het |
Anks1b |
A |
G |
10: 90,516,654 (GRCm39) |
Y883C |
probably damaging |
Het |
Atp11b |
T |
C |
3: 35,885,652 (GRCm39) |
F882L |
possibly damaging |
Het |
Atrn |
T |
A |
2: 130,806,807 (GRCm39) |
H609Q |
probably benign |
Het |
Bcl2l13 |
A |
T |
6: 120,842,646 (GRCm39) |
K113M |
possibly damaging |
Het |
Brinp2 |
T |
A |
1: 158,074,450 (GRCm39) |
N557I |
probably damaging |
Het |
C4b |
A |
G |
17: 34,959,326 (GRCm39) |
L416P |
probably benign |
Het |
Ccdc125 |
T |
A |
13: 100,819,327 (GRCm39) |
I163K |
possibly damaging |
Het |
Ccdc136 |
T |
G |
6: 29,420,033 (GRCm39) |
D1075E |
probably benign |
Het |
Cdc45 |
T |
A |
16: 18,629,203 (GRCm39) |
Y47F |
probably damaging |
Het |
Cdk10 |
T |
C |
8: 123,953,105 (GRCm39) |
V36A |
probably damaging |
Het |
Ciz1 |
T |
A |
2: 32,260,139 (GRCm39) |
|
probably null |
Het |
Clasp1 |
T |
G |
1: 118,530,144 (GRCm39) |
L1502* |
probably null |
Het |
Crtc1 |
G |
T |
8: 70,840,251 (GRCm39) |
Q541K |
probably benign |
Het |
Ddx5 |
G |
T |
11: 106,675,261 (GRCm39) |
T358N |
probably damaging |
Het |
Ehbp1l1 |
A |
T |
19: 5,766,452 (GRCm39) |
V1297E |
probably benign |
Het |
Eif2d |
C |
A |
1: 131,082,950 (GRCm39) |
T98K |
probably damaging |
Het |
Ezh2 |
T |
C |
6: 47,533,077 (GRCm39) |
D124G |
probably damaging |
Het |
Gamt |
T |
G |
10: 80,094,243 (GRCm39) |
I223L |
possibly damaging |
Het |
Gbp7 |
T |
C |
3: 142,240,402 (GRCm39) |
V40A |
probably damaging |
Het |
Gm11992 |
A |
G |
11: 8,999,165 (GRCm39) |
E7G |
probably damaging |
Het |
Gml2 |
A |
G |
15: 74,692,379 (GRCm39) |
|
probably null |
Het |
Grem2 |
A |
G |
1: 174,664,813 (GRCm39) |
V12A |
probably benign |
Het |
Gsta1 |
T |
A |
9: 78,139,577 (GRCm39) |
I19N |
probably damaging |
Het |
Gstt2 |
T |
C |
10: 75,667,736 (GRCm39) |
I240V |
probably benign |
Het |
Hectd4 |
T |
C |
5: 121,392,291 (GRCm39) |
L185S |
possibly damaging |
Het |
Hsd3b7 |
G |
A |
7: 127,400,419 (GRCm39) |
|
probably null |
Het |
Ift22 |
T |
A |
5: 136,940,638 (GRCm39) |
M101K |
probably benign |
Het |
Irs1 |
A |
G |
1: 82,267,802 (GRCm39) |
V138A |
probably benign |
Het |
Ky |
A |
G |
9: 102,419,141 (GRCm39) |
M383V |
possibly damaging |
Het |
Lama4 |
A |
G |
10: 38,946,005 (GRCm39) |
E796G |
probably damaging |
Het |
Lcp2 |
A |
G |
11: 34,038,061 (GRCm39) |
Y426C |
probably damaging |
Het |
Lig3 |
A |
G |
11: 82,688,601 (GRCm39) |
D755G |
probably damaging |
Het |
Lrrc43 |
A |
G |
5: 123,639,084 (GRCm39) |
D371G |
probably benign |
Het |
Lrrc43 |
T |
A |
5: 123,630,470 (GRCm39) |
I111N |
probably damaging |
Het |
Lrrc74b |
C |
A |
16: 17,376,213 (GRCm39) |
G146* |
probably null |
Het |
Lrrfip1 |
A |
G |
1: 91,047,874 (GRCm39) |
K479E |
possibly damaging |
Het |
Lrriq1 |
C |
A |
10: 103,051,055 (GRCm39) |
E566* |
probably null |
Het |
Mlxipl |
C |
T |
5: 135,161,263 (GRCm39) |
A394V |
possibly damaging |
Het |
Myh14 |
T |
C |
7: 44,281,819 (GRCm39) |
Y813C |
probably damaging |
Het |
Nat10 |
T |
A |
2: 103,555,490 (GRCm39) |
E943D |
probably benign |
Het |
Nectin2 |
T |
A |
7: 19,466,912 (GRCm39) |
K226* |
probably null |
Het |
Nlrc5 |
T |
G |
8: 95,219,720 (GRCm39) |
S1103R |
probably benign |
Het |
Nr4a1 |
T |
A |
15: 101,169,641 (GRCm39) |
Y304N |
probably damaging |
Het |
Ntpcr |
T |
C |
8: 126,474,483 (GRCm39) |
V184A |
probably benign |
Het |
Or1j13 |
T |
A |
2: 36,369,345 (GRCm39) |
N266Y |
probably damaging |
Het |
Or5p73 |
T |
C |
7: 108,064,978 (GRCm39) |
V149A |
probably benign |
Het |
Or5t18 |
A |
G |
2: 86,637,191 (GRCm39) |
S51P |
probably benign |
Het |
Oxr1 |
A |
C |
15: 41,517,030 (GRCm39) |
S65R |
possibly damaging |
Het |
Pcdhb19 |
A |
T |
18: 37,630,720 (GRCm39) |
I172L |
probably benign |
Het |
Pds5a |
A |
T |
5: 65,795,925 (GRCm39) |
I655N |
possibly damaging |
Het |
Pik3cg |
T |
C |
12: 32,250,516 (GRCm39) |
Y757C |
probably benign |
Het |
Plekha5 |
C |
A |
6: 140,472,184 (GRCm39) |
T37N |
possibly damaging |
Het |
Ppp4r1 |
C |
T |
17: 66,136,394 (GRCm39) |
A534V |
probably damaging |
Het |
Ppp4r1 |
T |
A |
17: 66,118,298 (GRCm39) |
F167I |
probably benign |
Het |
Ppt2 |
T |
A |
17: 34,846,300 (GRCm39) |
|
probably null |
Het |
Prrt2 |
A |
T |
7: 126,619,219 (GRCm39) |
V82D |
possibly damaging |
Het |
Rassf5 |
T |
A |
1: 131,108,366 (GRCm39) |
Y338F |
probably benign |
Het |
Rbbp6 |
G |
A |
7: 122,596,251 (GRCm39) |
V560I |
possibly damaging |
Het |
Rcbtb1 |
T |
C |
14: 59,474,127 (GRCm39) |
M90T |
unknown |
Het |
Rif1 |
T |
A |
2: 51,968,399 (GRCm39) |
L194* |
probably null |
Het |
Rybp |
A |
T |
6: 100,209,879 (GRCm39) |
I128K |
possibly damaging |
Het |
Samm50 |
T |
G |
15: 84,098,346 (GRCm39) |
F462V |
possibly damaging |
Het |
Slain1 |
T |
C |
14: 103,923,200 (GRCm39) |
Y264H |
probably damaging |
Het |
Slc29a4 |
C |
T |
5: 142,691,156 (GRCm39) |
P12L |
probably benign |
Het |
Slc6a2 |
T |
C |
8: 93,720,766 (GRCm39) |
I461T |
possibly damaging |
Het |
Soat2 |
A |
G |
15: 102,069,106 (GRCm39) |
D377G |
probably damaging |
Het |
Spocd1 |
A |
G |
4: 129,823,893 (GRCm39) |
E230G |
|
Het |
Tbc1d30 |
T |
A |
10: 121,183,061 (GRCm39) |
K126* |
probably null |
Het |
Tgfbi |
T |
A |
13: 56,779,997 (GRCm39) |
F515L |
probably damaging |
Het |
Utf1 |
A |
G |
7: 139,524,704 (GRCm39) |
|
probably benign |
Het |
Vmn1r206 |
G |
T |
13: 22,804,471 (GRCm39) |
Y245* |
probably null |
Het |
Zfc3h1 |
C |
A |
10: 115,256,588 (GRCm39) |
Y1519* |
probably null |
Het |
Zfp248 |
A |
T |
6: 118,407,103 (GRCm39) |
L162H |
possibly damaging |
Het |
Zfp804a |
T |
A |
2: 82,086,917 (GRCm39) |
F249I |
probably damaging |
Het |
|
Other mutations in Vmn1r87 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01400:Vmn1r87
|
APN |
7 |
12,866,230 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01577:Vmn1r87
|
APN |
7 |
12,865,775 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02972:Vmn1r87
|
APN |
7 |
12,866,256 (GRCm39) |
nonsense |
probably null |
|
IGL03246:Vmn1r87
|
APN |
7 |
12,866,288 (GRCm39) |
utr 5 prime |
probably benign |
|
PIT4142001:Vmn1r87
|
UTSW |
7 |
12,866,112 (GRCm39) |
missense |
probably benign |
0.00 |
R0153:Vmn1r87
|
UTSW |
7 |
12,866,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R0502:Vmn1r87
|
UTSW |
7 |
12,865,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Vmn1r87
|
UTSW |
7 |
12,865,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R1589:Vmn1r87
|
UTSW |
7 |
12,865,703 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1731:Vmn1r87
|
UTSW |
7 |
12,865,703 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2027:Vmn1r87
|
UTSW |
7 |
12,865,823 (GRCm39) |
missense |
probably damaging |
0.99 |
R2044:Vmn1r87
|
UTSW |
7 |
12,865,748 (GRCm39) |
missense |
probably benign |
0.02 |
R3124:Vmn1r87
|
UTSW |
7 |
12,865,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R4208:Vmn1r87
|
UTSW |
7 |
12,866,185 (GRCm39) |
missense |
probably benign |
0.37 |
R4731:Vmn1r87
|
UTSW |
7 |
12,866,254 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4732:Vmn1r87
|
UTSW |
7 |
12,866,254 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4733:Vmn1r87
|
UTSW |
7 |
12,866,254 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5079:Vmn1r87
|
UTSW |
7 |
12,866,253 (GRCm39) |
missense |
probably benign |
0.01 |
R5125:Vmn1r87
|
UTSW |
7 |
12,865,792 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5178:Vmn1r87
|
UTSW |
7 |
12,865,792 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6599:Vmn1r87
|
UTSW |
7 |
12,865,886 (GRCm39) |
nonsense |
probably null |
|
R7067:Vmn1r87
|
UTSW |
7 |
12,865,849 (GRCm39) |
missense |
probably benign |
0.02 |
R7560:Vmn1r87
|
UTSW |
7 |
12,865,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Vmn1r87
|
UTSW |
7 |
12,865,613 (GRCm39) |
missense |
probably benign |
0.01 |
R8040:Vmn1r87
|
UTSW |
7 |
12,866,086 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8220:Vmn1r87
|
UTSW |
7 |
12,865,427 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9690:Vmn1r87
|
UTSW |
7 |
12,866,263 (GRCm39) |
missense |
probably benign |
0.01 |
X0028:Vmn1r87
|
UTSW |
7 |
12,865,910 (GRCm39) |
missense |
possibly damaging |
0.52 |
|