Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
A |
3: 121,921,786 (GRCm39) |
I1114N |
probably damaging |
Het |
Ache |
C |
A |
5: 137,288,449 (GRCm39) |
R52S |
possibly damaging |
Het |
AI182371 |
A |
T |
2: 34,975,714 (GRCm39) |
|
probably null |
Het |
Ankrd17 |
T |
C |
5: 90,406,325 (GRCm39) |
S1453G |
probably damaging |
Het |
Arvcf |
A |
G |
16: 18,218,845 (GRCm39) |
N508S |
probably damaging |
Het |
Aurkc |
A |
C |
7: 7,005,796 (GRCm39) |
D136A |
possibly damaging |
Het |
Bfsp2 |
A |
G |
9: 103,325,848 (GRCm39) |
M265T |
probably benign |
Het |
Bmpr1b |
T |
C |
3: 141,562,369 (GRCm39) |
T273A |
probably damaging |
Het |
Cacnb1 |
T |
C |
11: 97,896,578 (GRCm39) |
K406R |
probably damaging |
Het |
Calcoco2 |
C |
T |
11: 95,998,252 (GRCm39) |
|
probably benign |
Het |
Capza1 |
T |
C |
3: 104,748,209 (GRCm39) |
|
probably null |
Het |
Ccdc63 |
T |
A |
5: 122,251,265 (GRCm39) |
I382F |
probably damaging |
Het |
Cep350 |
A |
T |
1: 155,739,161 (GRCm39) |
N2227K |
probably benign |
Het |
Chia1 |
T |
A |
3: 106,036,333 (GRCm39) |
Y304* |
probably null |
Het |
Col5a2 |
G |
A |
1: 45,461,123 (GRCm39) |
P258L |
|
Het |
Cyp21a1 |
A |
G |
17: 35,023,285 (GRCm39) |
L30P |
probably damaging |
Het |
Dennd4b |
T |
A |
3: 90,186,523 (GRCm39) |
H1351Q |
probably benign |
Het |
Dnah9 |
T |
A |
11: 65,746,078 (GRCm39) |
I4012F |
possibly damaging |
Het |
Drd1 |
A |
G |
13: 54,207,290 (GRCm39) |
I301T |
possibly damaging |
Het |
Dzip1 |
T |
A |
14: 119,144,326 (GRCm39) |
H369L |
probably damaging |
Het |
Fgfrl1 |
T |
A |
5: 108,851,257 (GRCm39) |
M58K |
probably damaging |
Het |
Ftsj3 |
G |
T |
11: 106,141,660 (GRCm39) |
D529E |
probably benign |
Het |
Fut9 |
A |
T |
4: 25,619,861 (GRCm39) |
W318R |
probably damaging |
Het |
Gabrg3 |
A |
G |
7: 56,634,706 (GRCm39) |
I159T |
probably damaging |
Het |
Gabrr1 |
A |
T |
4: 33,146,972 (GRCm39) |
D53V |
probably benign |
Het |
Ggps1 |
A |
G |
13: 14,228,928 (GRCm39) |
V85A |
probably benign |
Het |
Gm5141 |
C |
T |
13: 62,924,854 (GRCm39) |
W18* |
probably null |
Het |
Grik5 |
T |
A |
7: 24,722,743 (GRCm39) |
T518S |
probably benign |
Het |
Hapln3 |
A |
T |
7: 78,767,378 (GRCm39) |
|
probably benign |
Het |
Hbs1l |
C |
T |
10: 21,243,584 (GRCm39) |
Q646* |
probably null |
Het |
Hmox1 |
T |
C |
8: 75,823,644 (GRCm39) |
I104T |
probably benign |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,413 (GRCm39) |
Y348C |
probably damaging |
Het |
Igf2r |
A |
T |
17: 12,920,131 (GRCm39) |
S1403T |
probably damaging |
Het |
Igf2r |
G |
A |
17: 12,923,524 (GRCm39) |
T1186M |
probably damaging |
Het |
Igfbp1 |
T |
C |
11: 7,148,333 (GRCm39) |
|
probably null |
Het |
Ikbip |
C |
A |
10: 90,919,092 (GRCm39) |
A35E |
probably benign |
Het |
Isca1 |
C |
T |
13: 59,917,497 (GRCm39) |
A8T |
probably damaging |
Het |
Itgb2 |
T |
C |
10: 77,401,022 (GRCm39) |
L754P |
probably damaging |
Het |
Itgb6 |
C |
T |
2: 60,458,247 (GRCm39) |
C502Y |
probably damaging |
Het |
Kdm3a |
A |
G |
6: 71,577,092 (GRCm39) |
V741A |
probably benign |
Het |
Kdsr |
T |
C |
1: 106,680,949 (GRCm39) |
D83G |
possibly damaging |
Het |
Kiz |
T |
A |
2: 146,784,037 (GRCm39) |
N523K |
|
Het |
Kmt2a |
T |
C |
9: 44,733,802 (GRCm39) |
|
probably benign |
Het |
Krt25 |
T |
C |
11: 99,212,064 (GRCm39) |
E191G |
probably benign |
Het |
Lipn |
A |
G |
19: 34,046,880 (GRCm39) |
I61V |
probably damaging |
Het |
Lmbr1l |
T |
A |
15: 98,807,150 (GRCm39) |
|
probably null |
Het |
Lrrc4c |
A |
G |
2: 97,459,826 (GRCm39) |
K151E |
probably benign |
Het |
Mab21l3 |
T |
C |
3: 101,730,774 (GRCm39) |
Q155R |
probably benign |
Het |
Mtfr2 |
G |
A |
10: 20,233,274 (GRCm39) |
R281H |
possibly damaging |
Het |
Muc5ac |
A |
G |
7: 141,343,493 (GRCm39) |
Y35C |
possibly damaging |
Het |
Myadm |
C |
T |
7: 3,345,433 (GRCm39) |
T65I |
probably benign |
Het |
Nap1l1 |
T |
C |
10: 111,328,710 (GRCm39) |
V213A |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,111,705 (GRCm39) |
D737G |
probably damaging |
Het |
Ndst4 |
T |
A |
3: 125,405,155 (GRCm39) |
V470D |
probably damaging |
Het |
Nek5 |
T |
A |
8: 22,601,226 (GRCm39) |
Y165F |
probably damaging |
Het |
Nek5 |
A |
T |
8: 22,610,859 (GRCm39) |
V48E |
probably damaging |
Het |
Nr6a1 |
T |
C |
2: 38,650,400 (GRCm39) |
I77V |
probably damaging |
Het |
Nvl |
A |
T |
1: 180,966,638 (GRCm39) |
D93E |
probably benign |
Het |
Or11a4 |
C |
A |
17: 37,536,346 (GRCm39) |
T110K |
possibly damaging |
Het |
Or2q1 |
A |
G |
6: 42,794,950 (GRCm39) |
T182A |
probably benign |
Het |
Or52e5 |
A |
G |
7: 104,718,599 (GRCm39) |
|
probably benign |
Het |
Or52k2 |
A |
T |
7: 102,253,637 (GRCm39) |
L25F |
probably damaging |
Het |
Or52p1 |
A |
T |
7: 104,266,873 (GRCm39) |
T4S |
probably benign |
Het |
Or6c68 |
A |
T |
10: 129,158,259 (GRCm39) |
I256F |
probably damaging |
Het |
Pla2g4c |
G |
A |
7: 13,073,627 (GRCm39) |
V225I |
probably benign |
Het |
Plppr4 |
T |
A |
3: 117,116,690 (GRCm39) |
N331I |
probably damaging |
Het |
Ptpn13 |
A |
G |
5: 103,727,671 (GRCm39) |
R2051G |
probably benign |
Het |
Rbm45 |
T |
C |
2: 76,209,068 (GRCm39) |
S346P |
probably damaging |
Het |
Samd14 |
A |
C |
11: 94,912,027 (GRCm39) |
D168A |
probably damaging |
Het |
Slc15a1 |
C |
T |
14: 121,724,091 (GRCm39) |
G172R |
probably benign |
Het |
Slco3a1 |
G |
T |
7: 73,934,248 (GRCm39) |
Y641* |
probably null |
Het |
Srcap |
G |
A |
7: 127,151,566 (GRCm39) |
R2027H |
probably damaging |
Het |
Stra8 |
A |
T |
6: 34,904,624 (GRCm39) |
|
probably benign |
Het |
Syt11 |
T |
C |
3: 88,655,011 (GRCm39) |
Y430C |
probably damaging |
Het |
Tanc1 |
T |
G |
2: 59,615,800 (GRCm39) |
V269G |
possibly damaging |
Het |
Tead1 |
A |
G |
7: 112,497,818 (GRCm39) |
N342S |
probably benign |
Het |
Tenm3 |
C |
T |
8: 48,732,095 (GRCm39) |
A1254T |
possibly damaging |
Het |
Txlnb |
A |
T |
10: 17,682,546 (GRCm39) |
N156I |
probably damaging |
Het |
Ufl1 |
A |
T |
4: 25,262,258 (GRCm39) |
S409R |
possibly damaging |
Het |
Usp17la |
A |
G |
7: 104,510,307 (GRCm39) |
H304R |
probably benign |
Het |
Vmn1r203 |
T |
A |
13: 22,708,691 (GRCm39) |
H157Q |
possibly damaging |
Het |
Vmn1r37 |
C |
T |
6: 66,709,231 (GRCm39) |
R249* |
probably null |
Het |
Vps39 |
A |
G |
2: 120,169,066 (GRCm39) |
S292P |
probably benign |
Het |
Wnk1 |
A |
G |
6: 120,013,959 (GRCm39) |
V212A |
probably damaging |
Het |
Xbp1 |
T |
C |
11: 5,474,741 (GRCm39) |
V161A |
probably benign |
Het |
Zfp113 |
T |
C |
5: 138,143,092 (GRCm39) |
Q386R |
probably damaging |
Het |
|
Other mutations in Vmn2r96 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00562:Vmn2r96
|
APN |
17 |
18,804,077 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00563:Vmn2r96
|
APN |
17 |
18,804,077 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00769:Vmn2r96
|
APN |
17 |
18,804,081 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01314:Vmn2r96
|
APN |
17 |
18,803,226 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01983:Vmn2r96
|
APN |
17 |
18,817,527 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02314:Vmn2r96
|
APN |
17 |
18,804,221 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02600:Vmn2r96
|
APN |
17 |
18,817,829 (GRCm39) |
missense |
probably benign |
|
IGL02672:Vmn2r96
|
APN |
17 |
18,818,376 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02750:Vmn2r96
|
APN |
17 |
18,802,851 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03068:Vmn2r96
|
APN |
17 |
18,803,137 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03411:Vmn2r96
|
APN |
17 |
18,806,634 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0316:Vmn2r96
|
UTSW |
17 |
18,802,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R0502:Vmn2r96
|
UTSW |
17 |
18,804,262 (GRCm39) |
missense |
probably benign |
|
R0580:Vmn2r96
|
UTSW |
17 |
18,802,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Vmn2r96
|
UTSW |
17 |
18,817,830 (GRCm39) |
missense |
probably benign |
0.05 |
R0789:Vmn2r96
|
UTSW |
17 |
18,802,738 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1462:Vmn2r96
|
UTSW |
17 |
18,817,660 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1462:Vmn2r96
|
UTSW |
17 |
18,817,660 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1660:Vmn2r96
|
UTSW |
17 |
18,817,988 (GRCm39) |
missense |
probably benign |
0.00 |
R1755:Vmn2r96
|
UTSW |
17 |
18,802,915 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1843:Vmn2r96
|
UTSW |
17 |
18,818,183 (GRCm39) |
missense |
probably benign |
0.14 |
R1943:Vmn2r96
|
UTSW |
17 |
18,806,664 (GRCm39) |
missense |
probably benign |
0.09 |
R1993:Vmn2r96
|
UTSW |
17 |
18,804,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R2018:Vmn2r96
|
UTSW |
17 |
18,804,263 (GRCm39) |
missense |
probably benign |
|
R2405:Vmn2r96
|
UTSW |
17 |
18,818,102 (GRCm39) |
missense |
probably damaging |
0.96 |
R3977:Vmn2r96
|
UTSW |
17 |
18,817,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R3979:Vmn2r96
|
UTSW |
17 |
18,817,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R4059:Vmn2r96
|
UTSW |
17 |
18,818,339 (GRCm39) |
missense |
probably benign |
0.20 |
R4693:Vmn2r96
|
UTSW |
17 |
18,803,270 (GRCm39) |
missense |
probably benign |
0.03 |
R4709:Vmn2r96
|
UTSW |
17 |
18,803,088 (GRCm39) |
missense |
probably benign |
0.36 |
R4776:Vmn2r96
|
UTSW |
17 |
18,817,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R4882:Vmn2r96
|
UTSW |
17 |
18,817,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R4920:Vmn2r96
|
UTSW |
17 |
18,802,918 (GRCm39) |
missense |
probably benign |
0.07 |
R5143:Vmn2r96
|
UTSW |
17 |
18,804,120 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5301:Vmn2r96
|
UTSW |
17 |
18,817,950 (GRCm39) |
missense |
probably damaging |
0.98 |
R5507:Vmn2r96
|
UTSW |
17 |
18,818,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Vmn2r96
|
UTSW |
17 |
18,804,221 (GRCm39) |
missense |
probably benign |
0.01 |
R6181:Vmn2r96
|
UTSW |
17 |
18,804,126 (GRCm39) |
missense |
probably benign |
|
R6339:Vmn2r96
|
UTSW |
17 |
18,804,124 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6404:Vmn2r96
|
UTSW |
17 |
18,817,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R6452:Vmn2r96
|
UTSW |
17 |
18,804,117 (GRCm39) |
missense |
probably benign |
0.07 |
R6749:Vmn2r96
|
UTSW |
17 |
18,818,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R6813:Vmn2r96
|
UTSW |
17 |
18,802,116 (GRCm39) |
missense |
probably benign |
0.04 |
R6851:Vmn2r96
|
UTSW |
17 |
18,802,800 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6944:Vmn2r96
|
UTSW |
17 |
18,817,891 (GRCm39) |
missense |
probably benign |
0.16 |
R6949:Vmn2r96
|
UTSW |
17 |
18,818,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R6962:Vmn2r96
|
UTSW |
17 |
18,818,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R6990:Vmn2r96
|
UTSW |
17 |
18,804,082 (GRCm39) |
missense |
probably benign |
|
R7149:Vmn2r96
|
UTSW |
17 |
18,817,989 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7346:Vmn2r96
|
UTSW |
17 |
18,803,029 (GRCm39) |
missense |
probably benign |
0.15 |
R7385:Vmn2r96
|
UTSW |
17 |
18,803,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7442:Vmn2r96
|
UTSW |
17 |
18,793,662 (GRCm39) |
missense |
probably benign |
0.02 |
R7509:Vmn2r96
|
UTSW |
17 |
18,802,995 (GRCm39) |
missense |
probably benign |
0.02 |
R7652:Vmn2r96
|
UTSW |
17 |
18,793,832 (GRCm39) |
missense |
probably benign |
|
R7659:Vmn2r96
|
UTSW |
17 |
18,793,749 (GRCm39) |
missense |
probably benign |
0.00 |
R7753:Vmn2r96
|
UTSW |
17 |
18,806,663 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7855:Vmn2r96
|
UTSW |
17 |
18,818,130 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8166:Vmn2r96
|
UTSW |
17 |
18,802,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R8260:Vmn2r96
|
UTSW |
17 |
18,804,243 (GRCm39) |
missense |
probably benign |
0.04 |
R8323:Vmn2r96
|
UTSW |
17 |
18,803,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R8787:Vmn2r96
|
UTSW |
17 |
18,818,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8837:Vmn2r96
|
UTSW |
17 |
18,802,888 (GRCm39) |
missense |
probably benign |
|
R9306:Vmn2r96
|
UTSW |
17 |
18,803,226 (GRCm39) |
missense |
probably benign |
0.00 |
R9481:Vmn2r96
|
UTSW |
17 |
18,793,621 (GRCm39) |
start gained |
probably benign |
|
R9626:Vmn2r96
|
UTSW |
17 |
18,793,758 (GRCm39) |
missense |
probably benign |
0.14 |
R9629:Vmn2r96
|
UTSW |
17 |
18,803,257 (GRCm39) |
missense |
probably benign |
0.15 |
Z1088:Vmn2r96
|
UTSW |
17 |
18,817,628 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1177:Vmn2r96
|
UTSW |
17 |
18,818,376 (GRCm39) |
missense |
probably benign |
0.02 |
|