Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
T |
C |
5: 8,763,229 (GRCm39) |
S586P |
probably damaging |
Het |
Abcc3 |
G |
A |
11: 94,266,028 (GRCm39) |
|
probably benign |
Het |
Ap5z1 |
G |
A |
5: 142,461,546 (GRCm39) |
R583H |
probably benign |
Het |
Arrb1 |
G |
T |
7: 99,247,708 (GRCm39) |
V346L |
probably benign |
Het |
Atrnl1 |
T |
A |
19: 57,661,573 (GRCm39) |
F518I |
probably benign |
Het |
Bank1 |
T |
A |
3: 135,799,127 (GRCm39) |
I405F |
probably damaging |
Het |
Cacna1c |
A |
G |
6: 118,607,224 (GRCm39) |
C1227R |
probably benign |
Het |
Cacna1h |
A |
G |
17: 25,607,602 (GRCm39) |
L905P |
probably damaging |
Het |
Cc2d1a |
A |
G |
8: 84,860,465 (GRCm39) |
Y826H |
probably benign |
Het |
Cenpo |
A |
G |
12: 4,266,643 (GRCm39) |
V155A |
probably benign |
Het |
Cnmd |
A |
G |
14: 79,898,863 (GRCm39) |
F63S |
probably damaging |
Het |
Cnn3 |
G |
A |
3: 121,248,600 (GRCm39) |
G72D |
probably damaging |
Het |
Cox10 |
A |
G |
11: 63,962,539 (GRCm39) |
S101P |
probably benign |
Het |
Ctdsp1 |
T |
C |
1: 74,433,806 (GRCm39) |
V129A |
probably damaging |
Het |
Cyp2d34 |
A |
T |
15: 82,502,807 (GRCm39) |
S140T |
probably benign |
Het |
Dennd5a |
G |
A |
7: 109,532,820 (GRCm39) |
H317Y |
possibly damaging |
Het |
Dnaaf9 |
A |
G |
2: 130,555,334 (GRCm39) |
F858S |
probably damaging |
Het |
Eef2 |
C |
CN |
10: 81,014,603 (GRCm39) |
|
probably null |
Het |
Enox1 |
T |
A |
14: 77,819,876 (GRCm39) |
D210E |
probably damaging |
Het |
Fam171a1 |
A |
G |
2: 3,198,464 (GRCm39) |
N190S |
probably damaging |
Het |
Fat2 |
T |
A |
11: 55,144,459 (GRCm39) |
K4138N |
possibly damaging |
Het |
Fat4 |
A |
T |
3: 39,011,623 (GRCm39) |
D2241V |
probably damaging |
Het |
Fbn1 |
C |
T |
2: 125,245,090 (GRCm39) |
V266I |
possibly damaging |
Het |
Foxf2 |
T |
A |
13: 31,811,188 (GRCm39) |
Y376N |
probably damaging |
Het |
Fras1 |
T |
A |
5: 96,900,857 (GRCm39) |
S3025R |
probably benign |
Het |
Gba1 |
T |
C |
3: 89,111,307 (GRCm39) |
I24T |
probably benign |
Het |
Gdpd5 |
A |
G |
7: 99,087,540 (GRCm39) |
D68G |
probably damaging |
Het |
Grid1 |
G |
A |
14: 34,544,576 (GRCm39) |
S49N |
probably benign |
Het |
Grtp1 |
T |
C |
8: 13,229,639 (GRCm39) |
T250A |
possibly damaging |
Het |
Gucy1b1 |
T |
C |
3: 81,945,295 (GRCm39) |
N448D |
probably benign |
Het |
H2-Ob |
A |
G |
17: 34,463,100 (GRCm39) |
|
probably benign |
Het |
Hcn4 |
A |
G |
9: 58,730,795 (GRCm39) |
M1V |
probably null |
Het |
Hmcn2 |
G |
A |
2: 31,310,383 (GRCm39) |
A3326T |
probably damaging |
Het |
Impg2 |
TACCACCACCACCACCACCACCACCA |
TACCACCACCACCACCACCACCA |
16: 56,078,302 (GRCm39) |
|
probably benign |
Het |
Ippk |
C |
A |
13: 49,596,947 (GRCm39) |
Q254K |
probably damaging |
Het |
Itga2 |
A |
T |
13: 115,007,150 (GRCm39) |
L393I |
possibly damaging |
Het |
Kcna10 |
A |
T |
3: 107,102,575 (GRCm39) |
E402V |
possibly damaging |
Het |
Kcnab1 |
G |
A |
3: 65,205,141 (GRCm39) |
D119N |
probably damaging |
Het |
Kcnip4 |
T |
A |
5: 48,567,202 (GRCm39) |
T122S |
probably benign |
Het |
Kcnma1 |
G |
A |
14: 23,350,086 (GRCm39) |
P1151L |
probably damaging |
Het |
Klhl22 |
T |
A |
16: 17,610,453 (GRCm39) |
M568K |
probably benign |
Het |
Krt6a |
C |
T |
15: 101,601,183 (GRCm39) |
V257M |
probably damaging |
Het |
Ksr2 |
A |
C |
5: 117,693,290 (GRCm39) |
H246P |
probably damaging |
Het |
Lca5 |
T |
C |
9: 83,281,806 (GRCm39) |
D326G |
possibly damaging |
Het |
Lcp1 |
A |
G |
14: 75,451,928 (GRCm39) |
E393G |
probably benign |
Het |
Leo1 |
G |
A |
9: 75,352,831 (GRCm39) |
E125K |
probably benign |
Het |
Lipt1 |
T |
A |
1: 37,914,382 (GRCm39) |
V146E |
probably damaging |
Het |
Mael |
A |
T |
1: 166,062,968 (GRCm39) |
|
probably null |
Het |
Mga |
C |
T |
2: 119,778,442 (GRCm39) |
L1996F |
probably damaging |
Het |
Mllt6 |
A |
G |
11: 97,569,387 (GRCm39) |
N913S |
probably damaging |
Het |
Mphosph9 |
A |
C |
5: 124,436,822 (GRCm39) |
D507E |
probably damaging |
Het |
Mvp |
G |
A |
7: 126,586,728 (GRCm39) |
A801V |
probably benign |
Het |
Ndrg2 |
A |
G |
14: 52,146,119 (GRCm39) |
|
probably benign |
Het |
Neb |
T |
C |
2: 52,182,707 (GRCm39) |
D1053G |
possibly damaging |
Het |
Nubp1 |
C |
A |
16: 10,231,585 (GRCm39) |
L79I |
probably benign |
Het |
Or1e1f |
G |
A |
11: 73,856,246 (GRCm39) |
E271K |
probably benign |
Het |
Or1o2 |
A |
C |
17: 37,543,223 (GRCm39) |
L13V |
probably benign |
Het |
Or8d2 |
G |
A |
9: 38,759,805 (GRCm39) |
V132I |
probably benign |
Het |
Pnpla8 |
G |
A |
12: 44,330,188 (GRCm39) |
V29M |
probably benign |
Het |
Psmb2 |
T |
A |
4: 126,601,350 (GRCm39) |
I151N |
possibly damaging |
Het |
Ptgs2 |
C |
T |
1: 149,977,105 (GRCm39) |
T104I |
probably benign |
Het |
Ptpro |
A |
G |
6: 137,345,077 (GRCm39) |
T28A |
probably benign |
Het |
Raf1 |
A |
G |
6: 115,603,671 (GRCm39) |
|
probably null |
Het |
Ranbp2 |
T |
C |
10: 58,301,351 (GRCm39) |
M668T |
probably benign |
Het |
Rbm48 |
A |
T |
5: 3,641,760 (GRCm39) |
|
probably null |
Het |
Rhag |
A |
T |
17: 41,142,469 (GRCm39) |
T225S |
possibly damaging |
Het |
Rhof |
A |
C |
5: 123,269,950 (GRCm39) |
L69R |
probably damaging |
Het |
Slc24a5 |
T |
C |
2: 124,910,724 (GRCm39) |
S52P |
probably damaging |
Het |
Slc8a2 |
T |
C |
7: 15,875,039 (GRCm39) |
V429A |
probably damaging |
Het |
Slfn10-ps |
G |
A |
11: 82,926,388 (GRCm39) |
|
noncoding transcript |
Het |
Spam1 |
G |
A |
6: 24,796,886 (GRCm39) |
R279H |
probably damaging |
Het |
Srfbp1 |
A |
G |
18: 52,620,588 (GRCm39) |
D102G |
probably damaging |
Het |
Srrm3 |
A |
C |
5: 135,902,136 (GRCm39) |
|
probably benign |
Het |
Tk1 |
T |
C |
11: 117,712,933 (GRCm39) |
E98G |
probably damaging |
Het |
Trim13 |
G |
A |
14: 61,843,149 (GRCm39) |
V389I |
probably benign |
Het |
Ttc28 |
A |
T |
5: 111,383,366 (GRCm39) |
Y1289F |
probably benign |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Ugt1a10 |
T |
A |
1: 87,983,904 (GRCm39) |
V234D |
probably benign |
Het |
Vmn2r75 |
C |
T |
7: 85,814,575 (GRCm39) |
G306E |
probably benign |
Het |
Vmn2r86 |
C |
T |
10: 130,289,497 (GRCm39) |
V133I |
probably benign |
Het |
Vps13c |
C |
A |
9: 67,841,758 (GRCm39) |
Q1927K |
probably benign |
Het |
Zbtb14 |
C |
A |
17: 69,695,497 (GRCm39) |
F398L |
probably damaging |
Het |
Zfp219 |
T |
A |
14: 52,244,395 (GRCm39) |
T550S |
probably benign |
Het |
Zfp329 |
T |
A |
7: 12,545,395 (GRCm39) |
N43I |
probably benign |
Het |
Zfp507 |
G |
A |
7: 35,502,048 (GRCm39) |
|
probably benign |
Het |
Zfp97 |
T |
A |
17: 17,365,552 (GRCm39) |
F350L |
possibly damaging |
Het |
|
Other mutations in Vmn2r18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01098:Vmn2r18
|
APN |
5 |
151,496,296 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01564:Vmn2r18
|
APN |
5 |
151,508,633 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01602:Vmn2r18
|
APN |
5 |
151,510,106 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01605:Vmn2r18
|
APN |
5 |
151,510,106 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL01619:Vmn2r18
|
APN |
5 |
151,510,229 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02177:Vmn2r18
|
APN |
5 |
151,510,274 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02682:Vmn2r18
|
APN |
5 |
151,508,102 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02751:Vmn2r18
|
APN |
5 |
151,508,072 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02977:Vmn2r18
|
APN |
5 |
151,510,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Vmn2r18
|
UTSW |
5 |
151,508,269 (GRCm39) |
missense |
probably benign |
0.00 |
R0282:Vmn2r18
|
UTSW |
5 |
151,508,668 (GRCm39) |
missense |
probably benign |
0.02 |
R0529:Vmn2r18
|
UTSW |
5 |
151,485,988 (GRCm39) |
missense |
probably damaging |
0.99 |
R1467:Vmn2r18
|
UTSW |
5 |
151,510,301 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1467:Vmn2r18
|
UTSW |
5 |
151,510,301 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1506:Vmn2r18
|
UTSW |
5 |
151,499,099 (GRCm39) |
splice site |
probably null |
|
R1562:Vmn2r18
|
UTSW |
5 |
151,510,301 (GRCm39) |
missense |
probably benign |
0.12 |
R1637:Vmn2r18
|
UTSW |
5 |
151,508,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R1651:Vmn2r18
|
UTSW |
5 |
151,485,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R1883:Vmn2r18
|
UTSW |
5 |
151,499,190 (GRCm39) |
missense |
probably benign |
0.37 |
R1884:Vmn2r18
|
UTSW |
5 |
151,499,190 (GRCm39) |
missense |
probably benign |
0.37 |
R1914:Vmn2r18
|
UTSW |
5 |
151,499,286 (GRCm39) |
missense |
probably benign |
0.02 |
R2051:Vmn2r18
|
UTSW |
5 |
151,486,016 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2056:Vmn2r18
|
UTSW |
5 |
151,508,160 (GRCm39) |
missense |
probably damaging |
0.98 |
R2252:Vmn2r18
|
UTSW |
5 |
151,508,441 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2265:Vmn2r18
|
UTSW |
5 |
151,510,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R2266:Vmn2r18
|
UTSW |
5 |
151,510,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R2267:Vmn2r18
|
UTSW |
5 |
151,510,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R2843:Vmn2r18
|
UTSW |
5 |
151,485,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R3023:Vmn2r18
|
UTSW |
5 |
151,485,148 (GRCm39) |
missense |
probably benign |
0.13 |
R3694:Vmn2r18
|
UTSW |
5 |
151,508,033 (GRCm39) |
missense |
probably benign |
0.00 |
R3763:Vmn2r18
|
UTSW |
5 |
151,508,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R3816:Vmn2r18
|
UTSW |
5 |
151,485,148 (GRCm39) |
missense |
probably benign |
0.13 |
R4007:Vmn2r18
|
UTSW |
5 |
151,508,711 (GRCm39) |
missense |
probably damaging |
0.99 |
R4152:Vmn2r18
|
UTSW |
5 |
151,485,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R4308:Vmn2r18
|
UTSW |
5 |
151,508,268 (GRCm39) |
nonsense |
probably null |
|
R4362:Vmn2r18
|
UTSW |
5 |
151,496,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R4618:Vmn2r18
|
UTSW |
5 |
151,508,424 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4716:Vmn2r18
|
UTSW |
5 |
151,485,602 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4817:Vmn2r18
|
UTSW |
5 |
151,508,897 (GRCm39) |
splice site |
probably null |
|
R5111:Vmn2r18
|
UTSW |
5 |
151,485,913 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5692:Vmn2r18
|
UTSW |
5 |
151,485,724 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6115:Vmn2r18
|
UTSW |
5 |
151,508,462 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6244:Vmn2r18
|
UTSW |
5 |
151,508,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R6595:Vmn2r18
|
UTSW |
5 |
151,485,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R6997:Vmn2r18
|
UTSW |
5 |
151,485,338 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7227:Vmn2r18
|
UTSW |
5 |
151,496,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R7349:Vmn2r18
|
UTSW |
5 |
151,485,682 (GRCm39) |
nonsense |
probably null |
|
R7506:Vmn2r18
|
UTSW |
5 |
151,508,485 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7590:Vmn2r18
|
UTSW |
5 |
151,485,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7721:Vmn2r18
|
UTSW |
5 |
151,510,158 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7877:Vmn2r18
|
UTSW |
5 |
151,508,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R7882:Vmn2r18
|
UTSW |
5 |
151,485,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R7984:Vmn2r18
|
UTSW |
5 |
151,485,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R8295:Vmn2r18
|
UTSW |
5 |
151,508,621 (GRCm39) |
missense |
probably damaging |
0.97 |
R8353:Vmn2r18
|
UTSW |
5 |
151,485,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R8453:Vmn2r18
|
UTSW |
5 |
151,485,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R8670:Vmn2r18
|
UTSW |
5 |
151,485,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Vmn2r18
|
UTSW |
5 |
151,508,462 (GRCm39) |
missense |
probably damaging |
0.99 |
R8727:Vmn2r18
|
UTSW |
5 |
151,508,462 (GRCm39) |
missense |
probably damaging |
0.99 |
R8895:Vmn2r18
|
UTSW |
5 |
151,485,140 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9286:Vmn2r18
|
UTSW |
5 |
151,499,175 (GRCm39) |
missense |
probably benign |
0.00 |
R9339:Vmn2r18
|
UTSW |
5 |
151,485,132 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Vmn2r18
|
UTSW |
5 |
151,508,498 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1187:Vmn2r18
|
UTSW |
5 |
151,508,497 (GRCm39) |
missense |
probably benign |
0.00 |
|