Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933430I17Rik |
A |
T |
4: 62,457,146 (GRCm39) |
N155I |
probably benign |
Het |
Abca14 |
A |
G |
7: 119,924,382 (GRCm39) |
Y1678C |
probably damaging |
Het |
Adamts19 |
A |
T |
18: 59,103,078 (GRCm39) |
R706S |
probably benign |
Het |
Adipor1 |
T |
C |
1: 134,350,771 (GRCm39) |
S7P |
probably benign |
Het |
Adss2 |
A |
G |
1: 177,597,544 (GRCm39) |
I372T |
probably damaging |
Het |
Arhgap15 |
T |
A |
2: 44,133,136 (GRCm39) |
D347E |
possibly damaging |
Het |
Arnt |
C |
T |
3: 95,355,704 (GRCm39) |
S16L |
possibly damaging |
Het |
Asb8 |
T |
C |
15: 98,034,097 (GRCm39) |
T153A |
possibly damaging |
Het |
Aspscr1 |
G |
T |
11: 120,580,034 (GRCm39) |
G191V |
probably null |
Het |
Atm |
T |
C |
9: 53,382,718 (GRCm39) |
H1957R |
probably damaging |
Het |
Atp13a5 |
A |
G |
16: 29,133,419 (GRCm39) |
Y411H |
probably damaging |
Het |
Cadm1 |
T |
G |
9: 47,761,633 (GRCm39) |
I411S |
probably damaging |
Het |
Cdh23 |
T |
A |
10: 60,246,652 (GRCm39) |
M927L |
probably benign |
Het |
Cdk15 |
A |
T |
1: 59,383,475 (GRCm39) |
R423W |
probably damaging |
Het |
Cep250 |
T |
A |
2: 155,818,301 (GRCm39) |
|
probably null |
Het |
Cfap43 |
T |
A |
19: 47,885,649 (GRCm39) |
Y322F |
probably benign |
Het |
Cfap54 |
T |
C |
10: 92,833,204 (GRCm39) |
S1141G |
probably benign |
Het |
Clnk |
T |
C |
5: 38,863,969 (GRCm39) |
Y428C |
possibly damaging |
Het |
Cnksr1 |
A |
G |
4: 133,955,727 (GRCm39) |
S668P |
probably benign |
Het |
Cpxm2 |
A |
T |
7: 131,663,876 (GRCm39) |
I349N |
probably damaging |
Het |
Csmd3 |
A |
G |
15: 47,868,035 (GRCm39) |
|
probably null |
Het |
Cstdc3 |
T |
C |
16: 36,132,927 (GRCm39) |
L68P |
possibly damaging |
Het |
Dnmt1 |
C |
T |
9: 20,838,442 (GRCm39) |
R207H |
probably benign |
Het |
Dph2 |
A |
T |
4: 117,749,041 (GRCm39) |
F5I |
probably damaging |
Het |
Dst |
T |
A |
1: 34,202,802 (GRCm39) |
F325L |
probably damaging |
Het |
Edem3 |
T |
C |
1: 151,680,076 (GRCm39) |
L474S |
probably damaging |
Het |
Emilin1 |
T |
A |
5: 31,075,160 (GRCm39) |
L467Q |
probably benign |
Het |
Fam170a |
G |
A |
18: 50,415,181 (GRCm39) |
E276K |
probably benign |
Het |
Farp1 |
A |
T |
14: 121,456,787 (GRCm39) |
|
probably null |
Het |
Fbrs |
A |
T |
7: 127,085,163 (GRCm39) |
T584S |
possibly damaging |
Het |
Fbxo22 |
T |
A |
9: 55,116,626 (GRCm39) |
|
probably null |
Het |
Fhod3 |
T |
G |
18: 25,223,522 (GRCm39) |
L956R |
probably damaging |
Het |
Fmo4 |
G |
A |
1: 162,631,259 (GRCm39) |
T236I |
probably benign |
Het |
Foxp4 |
C |
T |
17: 48,186,796 (GRCm39) |
R378Q |
unknown |
Het |
Gdf10 |
G |
A |
14: 33,654,710 (GRCm39) |
A406T |
probably benign |
Het |
Gm11444 |
A |
T |
11: 85,738,999 (GRCm39) |
|
probably benign |
Het |
Gm14443 |
T |
C |
2: 175,011,497 (GRCm39) |
I316M |
probably benign |
Het |
Has3 |
A |
T |
8: 107,605,435 (GRCm39) |
Y547F |
probably benign |
Het |
Hdhd2 |
A |
G |
18: 77,052,841 (GRCm39) |
T164A |
probably benign |
Het |
Hoxb9 |
T |
A |
11: 96,162,880 (GRCm39) |
D171E |
possibly damaging |
Het |
Hpx |
A |
G |
7: 105,245,603 (GRCm39) |
Y118H |
probably damaging |
Het |
Iqsec1 |
T |
C |
6: 90,647,441 (GRCm39) |
K858E |
probably damaging |
Het |
Kifc1 |
G |
A |
17: 34,103,685 (GRCm39) |
R195C |
probably benign |
Het |
Lama2 |
C |
A |
10: 26,857,594 (GRCm39) |
R3085L |
probably damaging |
Het |
Lyst |
C |
A |
13: 13,791,203 (GRCm39) |
A22E |
probably damaging |
Het |
Man2a1 |
T |
C |
17: 65,057,830 (GRCm39) |
F1079L |
probably benign |
Het |
Marco |
C |
T |
1: 120,412,593 (GRCm39) |
G303R |
probably damaging |
Het |
Marveld2 |
A |
C |
13: 100,733,858 (GRCm39) |
I536R |
probably damaging |
Het |
Mcm5 |
A |
G |
8: 75,848,257 (GRCm39) |
D502G |
probably benign |
Het |
Mdga1 |
A |
T |
17: 30,059,862 (GRCm39) |
L653Q |
probably damaging |
Het |
Mical2 |
A |
G |
7: 111,980,311 (GRCm39) |
D161G |
probably benign |
Het |
Mroh2a |
C |
T |
1: 88,165,213 (GRCm39) |
R445* |
probably null |
Het |
Mrpl46 |
A |
T |
7: 78,431,146 (GRCm39) |
|
probably null |
Het |
Nckipsd |
C |
A |
9: 108,691,863 (GRCm39) |
|
probably null |
Het |
Nek11 |
T |
C |
9: 105,170,916 (GRCm39) |
D373G |
probably benign |
Het |
Nle1 |
G |
A |
11: 82,795,068 (GRCm39) |
S321F |
probably benign |
Het |
Noxa1 |
A |
G |
2: 24,980,620 (GRCm39) |
S130P |
probably damaging |
Het |
Or10a5 |
A |
G |
7: 106,635,478 (GRCm39) |
T39A |
possibly damaging |
Het |
Or51v14 |
T |
A |
7: 103,260,618 (GRCm39) |
*314L |
probably null |
Het |
Or5l13 |
A |
T |
2: 87,779,809 (GRCm39) |
L256H |
probably damaging |
Het |
Or8b39 |
T |
A |
9: 37,996,419 (GRCm39) |
C96S |
probably damaging |
Het |
Parp3 |
T |
G |
9: 106,352,021 (GRCm39) |
|
probably null |
Het |
Pask |
A |
T |
1: 93,249,180 (GRCm39) |
I740N |
probably benign |
Het |
Pelp1 |
A |
G |
11: 70,289,347 (GRCm39) |
F221S |
probably damaging |
Het |
Pkd1l1 |
T |
G |
11: 8,824,161 (GRCm39) |
K1135Q |
probably benign |
Het |
Plcl2 |
A |
T |
17: 50,915,109 (GRCm39) |
Q706L |
probably damaging |
Het |
Psg26 |
T |
C |
7: 18,212,264 (GRCm39) |
T364A |
probably benign |
Het |
Ptprb |
C |
T |
10: 116,177,441 (GRCm39) |
T1047M |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rab37 |
C |
T |
11: 115,051,177 (GRCm39) |
A155V |
probably damaging |
Het |
Rbbp6 |
A |
C |
7: 122,601,168 (GRCm39) |
|
probably benign |
Het |
Rbmxl2 |
A |
G |
7: 106,809,405 (GRCm39) |
D230G |
probably benign |
Het |
Rsf1 |
CGGCGGCGGCGGCGGCGGCGGCGGCGGC |
CGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Sass6 |
G |
T |
3: 116,403,945 (GRCm39) |
K194N |
possibly damaging |
Het |
Sgpp1 |
T |
G |
12: 75,782,222 (GRCm39) |
D39A |
probably benign |
Het |
Shank3 |
T |
C |
15: 89,387,351 (GRCm39) |
V198A |
probably damaging |
Het |
Sin3a |
T |
A |
9: 57,012,893 (GRCm39) |
S591T |
probably damaging |
Het |
Slc12a6 |
C |
T |
2: 112,185,503 (GRCm39) |
T924I |
possibly damaging |
Het |
Sln |
T |
A |
9: 53,760,785 (GRCm39) |
I10N |
probably benign |
Het |
St3gal3 |
A |
T |
4: 117,797,268 (GRCm39) |
M309K |
probably damaging |
Het |
Syne2 |
T |
A |
12: 76,016,319 (GRCm39) |
D3301E |
probably benign |
Het |
Tgtp2 |
A |
G |
11: 48,949,919 (GRCm39) |
S218P |
probably damaging |
Het |
Tha1 |
C |
T |
11: 117,760,179 (GRCm39) |
|
probably benign |
Het |
Tmem102 |
A |
G |
11: 69,695,225 (GRCm39) |
V249A |
probably benign |
Het |
Top3b |
G |
A |
16: 16,702,166 (GRCm39) |
E268K |
possibly damaging |
Het |
Trip4 |
T |
C |
9: 65,746,307 (GRCm39) |
S530G |
possibly damaging |
Het |
Tut1 |
T |
A |
19: 8,936,677 (GRCm39) |
V167E |
probably damaging |
Het |
Tut4 |
A |
T |
4: 108,412,903 (GRCm39) |
S1535C |
probably damaging |
Het |
Ube2u |
A |
T |
4: 100,338,833 (GRCm39) |
M33L |
probably benign |
Het |
Unc79 |
T |
C |
12: 102,957,621 (GRCm39) |
I12T |
probably damaging |
Het |
Unc79 |
A |
T |
12: 103,041,178 (GRCm39) |
D737V |
probably benign |
Het |
Vmn1r26 |
A |
G |
6: 57,985,286 (GRCm39) |
V301A |
probably benign |
Het |
Vmn2r98 |
A |
C |
17: 19,286,680 (GRCm39) |
N393H |
possibly damaging |
Het |
Vps13b |
T |
G |
15: 35,878,835 (GRCm39) |
S2945A |
probably damaging |
Het |
Whrn |
C |
T |
4: 63,353,666 (GRCm39) |
R367H |
possibly damaging |
Het |
Zfp235 |
A |
T |
7: 23,839,771 (GRCm39) |
L133F |
probably damaging |
Het |
Zfp74 |
T |
C |
7: 29,635,136 (GRCm39) |
T191A |
probably benign |
Het |
Zfp943 |
A |
T |
17: 22,211,979 (GRCm39) |
K355I |
probably damaging |
Het |
Zranb1 |
T |
G |
7: 132,584,458 (GRCm39) |
S601R |
probably damaging |
Het |
Zscan29 |
A |
T |
2: 121,000,289 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Vmn1r86 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00492:Vmn1r86
|
APN |
7 |
12,836,468 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01124:Vmn1r86
|
APN |
7 |
12,836,856 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01291:Vmn1r86
|
APN |
7 |
12,836,433 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02347:Vmn1r86
|
APN |
7 |
12,836,574 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02457:Vmn1r86
|
APN |
7 |
12,836,707 (GRCm39) |
missense |
probably benign |
|
IGL02983:Vmn1r86
|
APN |
7 |
12,836,741 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU05:Vmn1r86
|
UTSW |
7 |
12,836,433 (GRCm39) |
missense |
probably benign |
0.14 |
R0304:Vmn1r86
|
UTSW |
7 |
12,836,707 (GRCm39) |
missense |
probably benign |
|
R0525:Vmn1r86
|
UTSW |
7 |
12,836,088 (GRCm39) |
missense |
probably benign |
0.13 |
R2227:Vmn1r86
|
UTSW |
7 |
12,836,847 (GRCm39) |
missense |
probably benign |
0.00 |
R3149:Vmn1r86
|
UTSW |
7 |
12,836,358 (GRCm39) |
nonsense |
probably null |
|
R3896:Vmn1r86
|
UTSW |
7 |
12,836,093 (GRCm39) |
missense |
probably benign |
0.18 |
R4735:Vmn1r86
|
UTSW |
7 |
12,836,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R5219:Vmn1r86
|
UTSW |
7 |
12,836,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R6003:Vmn1r86
|
UTSW |
7 |
12,836,125 (GRCm39) |
nonsense |
probably null |
|
R6457:Vmn1r86
|
UTSW |
7 |
12,836,279 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7442:Vmn1r86
|
UTSW |
7 |
12,835,983 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7622:Vmn1r86
|
UTSW |
7 |
12,836,685 (GRCm39) |
missense |
probably benign |
0.07 |
R8436:Vmn1r86
|
UTSW |
7 |
12,836,771 (GRCm39) |
missense |
probably benign |
0.25 |
R9141:Vmn1r86
|
UTSW |
7 |
12,836,789 (GRCm39) |
nonsense |
probably null |
|
R9374:Vmn1r86
|
UTSW |
7 |
12,836,781 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9398:Vmn1r86
|
UTSW |
7 |
12,836,261 (GRCm39) |
missense |
probably damaging |
0.98 |
R9551:Vmn1r86
|
UTSW |
7 |
12,836,781 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9552:Vmn1r86
|
UTSW |
7 |
12,836,781 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9606:Vmn1r86
|
UTSW |
7 |
12,836,741 (GRCm39) |
missense |
probably damaging |
1.00 |
|