Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310061N02Rik |
A |
G |
16: 88,504,651 (GRCm39) |
S49P |
possibly damaging |
Het |
Abcb1a |
T |
C |
5: 8,796,657 (GRCm39) |
|
probably null |
Het |
Adgb |
G |
A |
10: 10,274,647 (GRCm39) |
T770I |
probably damaging |
Het |
Adgre4 |
A |
T |
17: 56,098,491 (GRCm39) |
T134S |
probably benign |
Het |
Aldh1a1 |
A |
G |
19: 20,597,349 (GRCm39) |
N110S |
probably damaging |
Het |
Alox5 |
C |
A |
6: 116,437,964 (GRCm39) |
V8L |
possibly damaging |
Het |
Ambra1 |
A |
G |
2: 91,603,191 (GRCm39) |
T392A |
possibly damaging |
Het |
Apob |
A |
G |
12: 8,058,051 (GRCm39) |
I2145V |
probably benign |
Het |
Arhgap39 |
A |
G |
15: 76,625,717 (GRCm39) |
Y196H |
possibly damaging |
Het |
Armh2 |
A |
G |
13: 24,930,490 (GRCm39) |
|
probably benign |
Het |
Carmil1 |
A |
G |
13: 24,251,173 (GRCm39) |
L439S |
probably damaging |
Het |
Carmil1 |
A |
T |
13: 24,325,659 (GRCm39) |
S224T |
possibly damaging |
Het |
Cfh |
G |
A |
1: 140,028,561 (GRCm39) |
Q706* |
probably null |
Het |
Chd2 |
A |
C |
7: 73,118,325 (GRCm39) |
S1098A |
probably benign |
Het |
Chrna5 |
A |
T |
9: 54,911,985 (GRCm39) |
I158F |
probably damaging |
Het |
Cilk1 |
A |
G |
9: 78,060,975 (GRCm39) |
D207G |
probably damaging |
Het |
Col6a5 |
T |
C |
9: 105,807,983 (GRCm39) |
T1022A |
unknown |
Het |
Cul7 |
T |
A |
17: 46,967,976 (GRCm39) |
Y423* |
probably null |
Het |
Cyp2e1 |
T |
C |
7: 140,353,588 (GRCm39) |
Y342H |
probably benign |
Het |
D630045J12Rik |
T |
C |
6: 38,125,275 (GRCm39) |
K1580E |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,066,651 (GRCm39) |
M2573T |
probably damaging |
Het |
Dnai4 |
T |
C |
4: 102,929,881 (GRCm39) |
K370R |
possibly damaging |
Het |
Edem1 |
T |
A |
6: 108,805,707 (GRCm39) |
|
probably benign |
Het |
Erp29 |
C |
T |
5: 121,585,237 (GRCm39) |
E86K |
probably benign |
Het |
Esrp2 |
C |
A |
8: 106,859,141 (GRCm39) |
R535L |
probably damaging |
Het |
Gabrb2 |
C |
T |
11: 42,420,330 (GRCm39) |
|
probably benign |
Het |
Gpat3 |
C |
T |
5: 101,005,039 (GRCm39) |
P58L |
probably benign |
Het |
Herc1 |
T |
A |
9: 66,403,266 (GRCm39) |
V4395E |
possibly damaging |
Het |
Hivep2 |
C |
A |
10: 14,004,713 (GRCm39) |
T437K |
probably benign |
Het |
Hmgb2 |
G |
A |
8: 57,966,344 (GRCm39) |
C106Y |
probably damaging |
Het |
Hoxa10 |
T |
C |
6: 52,209,481 (GRCm39) |
|
probably benign |
Het |
Hsd3b1 |
T |
A |
3: 98,760,226 (GRCm39) |
Y255F |
probably benign |
Het |
Ighd |
T |
C |
12: 113,379,819 (GRCm39) |
K42E |
probably benign |
Het |
Ighv1-26 |
T |
C |
12: 114,752,191 (GRCm39) |
Y51C |
possibly damaging |
Het |
Ighv5-2 |
C |
T |
12: 113,542,419 (GRCm39) |
E19K |
possibly damaging |
Het |
Ipo11 |
T |
C |
13: 106,970,668 (GRCm39) |
|
probably benign |
Het |
Itk |
C |
T |
11: 46,235,658 (GRCm39) |
|
probably benign |
Het |
Kat6a |
T |
A |
8: 23,430,592 (GRCm39) |
H1982Q |
unknown |
Het |
Kdm4d |
C |
T |
9: 14,374,686 (GRCm39) |
V391I |
probably benign |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Lgr6 |
T |
A |
1: 134,949,544 (GRCm39) |
S229C |
probably benign |
Het |
Lhx9 |
T |
A |
1: 138,766,089 (GRCm39) |
Y233F |
possibly damaging |
Het |
Lmf1 |
G |
A |
17: 25,873,445 (GRCm39) |
V317M |
probably damaging |
Het |
Mapk4 |
T |
C |
18: 74,070,321 (GRCm39) |
T191A |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Naglu |
C |
T |
11: 100,961,932 (GRCm39) |
T135M |
probably damaging |
Het |
Nomo1 |
T |
A |
7: 45,693,643 (GRCm39) |
|
probably null |
Het |
Nop56 |
T |
A |
2: 130,119,784 (GRCm39) |
V75E |
possibly damaging |
Het |
Nr1i3 |
G |
A |
1: 171,046,164 (GRCm39) |
C283Y |
probably damaging |
Het |
Or4x6 |
T |
A |
2: 89,949,174 (GRCm39) |
Y256F |
possibly damaging |
Het |
Or51d1 |
G |
A |
7: 102,347,933 (GRCm39) |
G163R |
probably damaging |
Het |
Or6c38 |
T |
G |
10: 128,929,489 (GRCm39) |
Y118S |
probably damaging |
Het |
Pcdhga2 |
A |
G |
18: 37,802,452 (GRCm39) |
S99G |
probably benign |
Het |
Pcnx1 |
T |
A |
12: 81,965,925 (GRCm39) |
D697E |
probably damaging |
Het |
Plxnb1 |
G |
A |
9: 108,939,716 (GRCm39) |
D1462N |
probably damaging |
Het |
Pnn |
G |
T |
12: 59,118,991 (GRCm39) |
V525F |
possibly damaging |
Het |
Prrc2a |
A |
T |
17: 35,375,463 (GRCm39) |
D1062E |
probably damaging |
Het |
Prss35 |
T |
A |
9: 86,637,722 (GRCm39) |
V164E |
probably damaging |
Het |
Psapl1 |
T |
C |
5: 36,362,547 (GRCm39) |
S380P |
probably benign |
Het |
Rnf222 |
A |
T |
11: 68,783,845 (GRCm39) |
E137D |
probably damaging |
Het |
Rsph10b |
A |
G |
5: 143,874,135 (GRCm39) |
T79A |
probably damaging |
Het |
Sbf2 |
T |
C |
7: 109,950,817 (GRCm39) |
Q1164R |
probably damaging |
Het |
Scn7a |
T |
C |
2: 66,556,592 (GRCm39) |
D331G |
probably damaging |
Het |
Shtn1 |
G |
C |
19: 59,039,305 (GRCm39) |
R45G |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,438,519 (GRCm39) |
S1529N |
probably benign |
Het |
St8sia3 |
T |
A |
18: 64,398,634 (GRCm39) |
V31E |
probably benign |
Het |
Sult1b1 |
A |
T |
5: 87,662,906 (GRCm39) |
W265R |
probably damaging |
Het |
Supt5 |
G |
T |
7: 28,015,754 (GRCm39) |
Q863K |
probably benign |
Het |
Tbc1d31 |
A |
G |
15: 57,804,124 (GRCm39) |
R380G |
probably benign |
Het |
Tdpoz1 |
T |
A |
3: 93,577,845 (GRCm39) |
D313V |
possibly damaging |
Het |
Tmem260 |
CAGGGACCGGCATAG |
CAG |
14: 48,749,451 (GRCm39) |
|
probably benign |
Het |
Tpx2 |
A |
T |
2: 152,727,016 (GRCm39) |
T428S |
probably damaging |
Het |
Trip11 |
A |
T |
12: 101,851,705 (GRCm39) |
H786Q |
probably benign |
Het |
Trpc6 |
A |
T |
9: 8,626,615 (GRCm39) |
M322L |
probably benign |
Het |
Try10 |
T |
C |
6: 41,332,386 (GRCm39) |
V14A |
probably benign |
Het |
Unc13d |
A |
T |
11: 115,961,108 (GRCm39) |
F416L |
probably damaging |
Het |
Zbp1 |
A |
G |
2: 173,051,006 (GRCm39) |
F288S |
probably damaging |
Het |
Zc3h11a |
T |
A |
1: 133,568,436 (GRCm39) |
Q71L |
probably damaging |
Het |
Zfp40 |
G |
A |
17: 23,396,008 (GRCm39) |
T193I |
possibly damaging |
Het |
Zfp607a |
T |
C |
7: 27,578,078 (GRCm39) |
Y383H |
probably benign |
Het |
Zfp622 |
T |
A |
15: 25,987,128 (GRCm39) |
Y82* |
probably null |
Het |
Zfp964 |
T |
C |
8: 70,116,665 (GRCm39) |
F422L |
probably benign |
Het |
|
Other mutations in Vmn2r75 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01133:Vmn2r75
|
APN |
7 |
85,797,240 (GRCm39) |
unclassified |
probably benign |
|
IGL01287:Vmn2r75
|
APN |
7 |
85,797,801 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01318:Vmn2r75
|
APN |
7 |
85,814,774 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01331:Vmn2r75
|
APN |
7 |
85,820,870 (GRCm39) |
nonsense |
probably null |
|
IGL01406:Vmn2r75
|
APN |
7 |
85,812,500 (GRCm39) |
splice site |
probably benign |
|
IGL01615:Vmn2r75
|
APN |
7 |
85,797,681 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01657:Vmn2r75
|
APN |
7 |
85,813,455 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02237:Vmn2r75
|
APN |
7 |
85,814,786 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02275:Vmn2r75
|
APN |
7 |
85,814,348 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02307:Vmn2r75
|
APN |
7 |
85,814,974 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03136:Vmn2r75
|
APN |
7 |
85,797,911 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03160:Vmn2r75
|
APN |
7 |
85,797,644 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03244:Vmn2r75
|
APN |
7 |
85,820,933 (GRCm39) |
unclassified |
probably benign |
|
PIT4449001:Vmn2r75
|
UTSW |
7 |
85,814,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Vmn2r75
|
UTSW |
7 |
85,797,309 (GRCm39) |
nonsense |
probably null |
|
R0049:Vmn2r75
|
UTSW |
7 |
85,797,309 (GRCm39) |
nonsense |
probably null |
|
R0083:Vmn2r75
|
UTSW |
7 |
85,814,866 (GRCm39) |
missense |
probably benign |
0.00 |
R0108:Vmn2r75
|
UTSW |
7 |
85,814,866 (GRCm39) |
missense |
probably benign |
0.00 |
R0276:Vmn2r75
|
UTSW |
7 |
85,797,515 (GRCm39) |
missense |
probably benign |
0.01 |
R0320:Vmn2r75
|
UTSW |
7 |
85,814,288 (GRCm39) |
missense |
probably benign |
0.36 |
R0471:Vmn2r75
|
UTSW |
7 |
85,814,721 (GRCm39) |
missense |
probably benign |
0.01 |
R0562:Vmn2r75
|
UTSW |
7 |
85,797,449 (GRCm39) |
nonsense |
probably null |
|
R0631:Vmn2r75
|
UTSW |
7 |
85,812,478 (GRCm39) |
missense |
probably null |
1.00 |
R0661:Vmn2r75
|
UTSW |
7 |
85,814,866 (GRCm39) |
missense |
probably benign |
0.00 |
R0811:Vmn2r75
|
UTSW |
7 |
85,814,575 (GRCm39) |
missense |
probably benign |
0.38 |
R0812:Vmn2r75
|
UTSW |
7 |
85,814,575 (GRCm39) |
missense |
probably benign |
0.38 |
R0891:Vmn2r75
|
UTSW |
7 |
85,813,476 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1340:Vmn2r75
|
UTSW |
7 |
85,797,798 (GRCm39) |
missense |
probably damaging |
0.98 |
R1501:Vmn2r75
|
UTSW |
7 |
85,814,850 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1760:Vmn2r75
|
UTSW |
7 |
85,798,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Vmn2r75
|
UTSW |
7 |
85,797,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Vmn2r75
|
UTSW |
7 |
85,814,372 (GRCm39) |
missense |
probably benign |
0.00 |
R2292:Vmn2r75
|
UTSW |
7 |
85,798,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R3688:Vmn2r75
|
UTSW |
7 |
85,797,629 (GRCm39) |
missense |
probably damaging |
0.99 |
R3892:Vmn2r75
|
UTSW |
7 |
85,813,494 (GRCm39) |
missense |
probably null |
1.00 |
R4532:Vmn2r75
|
UTSW |
7 |
85,797,349 (GRCm39) |
nonsense |
probably null |
|
R4583:Vmn2r75
|
UTSW |
7 |
85,813,290 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4592:Vmn2r75
|
UTSW |
7 |
85,815,494 (GRCm39) |
missense |
probably benign |
0.00 |
R4859:Vmn2r75
|
UTSW |
7 |
85,797,611 (GRCm39) |
missense |
probably benign |
0.35 |
R4896:Vmn2r75
|
UTSW |
7 |
85,820,787 (GRCm39) |
missense |
probably benign |
0.01 |
R4943:Vmn2r75
|
UTSW |
7 |
85,814,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Vmn2r75
|
UTSW |
7 |
85,815,375 (GRCm39) |
critical splice donor site |
probably null |
|
R5048:Vmn2r75
|
UTSW |
7 |
85,814,735 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5063:Vmn2r75
|
UTSW |
7 |
85,813,372 (GRCm39) |
missense |
probably benign |
|
R5156:Vmn2r75
|
UTSW |
7 |
85,813,436 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5243:Vmn2r75
|
UTSW |
7 |
85,813,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R5277:Vmn2r75
|
UTSW |
7 |
85,815,500 (GRCm39) |
missense |
probably benign |
|
R5574:Vmn2r75
|
UTSW |
7 |
85,815,510 (GRCm39) |
missense |
probably benign |
0.22 |
R5622:Vmn2r75
|
UTSW |
7 |
85,797,702 (GRCm39) |
missense |
probably benign |
0.15 |
R5680:Vmn2r75
|
UTSW |
7 |
85,820,779 (GRCm39) |
missense |
probably benign |
0.10 |
R5884:Vmn2r75
|
UTSW |
7 |
85,814,578 (GRCm39) |
missense |
probably benign |
|
R6021:Vmn2r75
|
UTSW |
7 |
85,820,820 (GRCm39) |
missense |
probably benign |
0.01 |
R6217:Vmn2r75
|
UTSW |
7 |
85,815,375 (GRCm39) |
critical splice donor site |
probably benign |
|
R6242:Vmn2r75
|
UTSW |
7 |
85,814,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Vmn2r75
|
UTSW |
7 |
85,814,482 (GRCm39) |
missense |
probably benign |
0.12 |
R6441:Vmn2r75
|
UTSW |
7 |
85,820,784 (GRCm39) |
missense |
probably damaging |
0.99 |
R6495:Vmn2r75
|
UTSW |
7 |
85,813,287 (GRCm39) |
missense |
probably benign |
0.00 |
R6553:Vmn2r75
|
UTSW |
7 |
85,813,453 (GRCm39) |
missense |
probably benign |
0.28 |
R6670:Vmn2r75
|
UTSW |
7 |
85,797,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R7078:Vmn2r75
|
UTSW |
7 |
85,815,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R7164:Vmn2r75
|
UTSW |
7 |
85,814,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R8411:Vmn2r75
|
UTSW |
7 |
85,797,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Vmn2r75
|
UTSW |
7 |
85,797,685 (GRCm39) |
nonsense |
probably null |
|
R8559:Vmn2r75
|
UTSW |
7 |
85,815,480 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8677:Vmn2r75
|
UTSW |
7 |
85,814,410 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8708:Vmn2r75
|
UTSW |
7 |
85,812,476 (GRCm39) |
missense |
probably damaging |
0.99 |
R8778:Vmn2r75
|
UTSW |
7 |
85,813,497 (GRCm39) |
missense |
probably benign |
0.40 |
R8968:Vmn2r75
|
UTSW |
7 |
85,820,765 (GRCm39) |
nonsense |
probably null |
|
R9145:Vmn2r75
|
UTSW |
7 |
85,813,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R9316:Vmn2r75
|
UTSW |
7 |
85,797,313 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9363:Vmn2r75
|
UTSW |
7 |
85,815,423 (GRCm39) |
missense |
probably benign |
0.03 |
|