Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A030005L19Rik |
GTGGCTGCT |
GTGGCTGCTTTGGCTGCT |
1: 82,891,293 (GRCm39) |
|
probably benign |
Het |
Abca15 |
T |
A |
7: 119,993,683 (GRCm39) |
V1301E |
possibly damaging |
Het |
Adcy10 |
T |
A |
1: 165,379,678 (GRCm39) |
V980E |
probably damaging |
Het |
Aldh1a2 |
T |
C |
9: 71,192,552 (GRCm39) |
V469A |
probably damaging |
Het |
Alk |
T |
A |
17: 72,256,808 (GRCm39) |
T684S |
probably benign |
Het |
Ankhd1 |
GGCGGC |
GGCGGCAGCGGC |
18: 36,693,965 (GRCm39) |
|
probably benign |
Het |
Anks1b |
G |
A |
10: 89,869,087 (GRCm39) |
G49D |
probably damaging |
Het |
Blm |
CCTCCTCC |
CCTCCTCCTCCTACTCCTCC |
7: 80,162,674 (GRCm39) |
|
probably null |
Het |
Btnl10 |
CAAA |
CAAAAAA |
11: 58,814,752 (GRCm39) |
|
probably benign |
Het |
Ccdc81 |
C |
A |
7: 89,515,906 (GRCm39) |
|
probably null |
Het |
Cd209g |
A |
G |
8: 4,187,398 (GRCm39) |
Y194C |
probably benign |
Het |
Cenpc1 |
A |
T |
5: 86,193,228 (GRCm39) |
S220R |
possibly damaging |
Het |
Ddx42 |
A |
T |
11: 106,123,630 (GRCm39) |
|
probably null |
Het |
Dock4 |
GTGCCGGTGCCCGT |
G |
12: 40,894,398 (GRCm39) |
|
probably null |
Het |
Eif5b |
A |
T |
1: 38,060,673 (GRCm39) |
|
probably null |
Het |
Ell2 |
C |
A |
13: 75,911,727 (GRCm39) |
H338N |
probably damaging |
Het |
Entpd2 |
CTT |
CTTT |
2: 25,290,907 (GRCm39) |
|
probably null |
Het |
Flywch1 |
CCACTCCTGGTGT |
CCACTCCTGGTGTGGGGAGGCTACGTACTCACGCACTCCTGGTGT |
17: 23,981,140 (GRCm39) |
|
probably null |
Het |
Gm8369 |
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG |
19: 11,489,106 (GRCm39) |
|
probably null |
Het |
Gnat2 |
T |
C |
3: 108,003,645 (GRCm39) |
S107P |
unknown |
Het |
Guk1 |
T |
A |
11: 59,077,234 (GRCm39) |
D70V |
probably benign |
Het |
Itpkb |
C |
T |
1: 180,160,887 (GRCm39) |
R338W |
probably damaging |
Het |
Krtap28-10 |
ACCACAGCCACAGCCACCACAGCCACAGCC |
ACCACAGCCACAGCCCCCACAGCCACAGCCACCACAGCCACAGCC |
1: 83,019,974 (GRCm39) |
|
probably benign |
Het |
Lamp3 |
A |
C |
16: 19,520,000 (GRCm39) |
I61R |
probably benign |
Het |
Lrch1 |
GCTGGTGGTGT |
G |
14: 75,184,995 (GRCm39) |
|
probably null |
Het |
Lrp1b |
C |
T |
2: 41,000,919 (GRCm39) |
E2216K |
|
Het |
Lrrc27 |
A |
G |
7: 138,806,016 (GRCm39) |
D227G |
probably benign |
Het |
Lrrk1 |
C |
T |
7: 66,031,250 (GRCm39) |
G16E |
possibly damaging |
Het |
Lrrtm1 |
T |
A |
6: 77,221,334 (GRCm39) |
S264T |
possibly damaging |
Het |
Lypd8 |
CCAATCACCAACA |
CCAATCACCAACAGTTTCCTCGCCTCTGTTACCCCACCAATCACCAACA |
11: 58,281,058 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
CAG |
CAGAAG |
X: 70,162,455 (GRCm39) |
|
probably benign |
Het |
Mpo |
G |
C |
11: 87,688,465 (GRCm39) |
A375P |
probably damaging |
Het |
Myo9a |
A |
G |
9: 59,776,869 (GRCm39) |
H1089R |
probably benign |
Het |
Nalf2 |
CGCCGC |
CGCCGCTGCCGC |
X: 98,864,967 (GRCm39) |
|
probably benign |
Het |
Ndufc2 |
T |
C |
7: 97,056,228 (GRCm39) |
*109Q |
probably null |
Het |
Nudt16 |
A |
T |
9: 105,008,898 (GRCm39) |
Y28N |
probably damaging |
Het |
Nudt4 |
A |
T |
10: 95,385,675 (GRCm39) |
|
probably null |
Het |
Nusap1 |
AGATACACGTTAGCAGTGAGGAGCAAGCTG |
AGATACACGTTAGCAGTGAGGAGCAAGCTGCGATACACGTTAGCAGTGAGGAGCAAGCTG |
2: 119,458,059 (GRCm39) |
|
probably benign |
Het |
Or2ag15 |
T |
A |
7: 106,340,692 (GRCm39) |
I150F |
probably benign |
Het |
P2ry12 |
T |
A |
3: 59,124,833 (GRCm39) |
T281S |
probably benign |
Het |
P4ha2 |
TGTTGG |
T |
11: 54,001,072 (GRCm39) |
|
probably null |
Het |
Pcnx2 |
A |
G |
8: 126,604,258 (GRCm39) |
V666A |
probably damaging |
Het |
Pde6a |
T |
A |
18: 61,364,475 (GRCm39) |
I177N |
possibly damaging |
Het |
Pgm1 |
A |
T |
4: 99,819,500 (GRCm39) |
|
probably null |
Het |
Plce1 |
T |
A |
19: 38,705,651 (GRCm39) |
W1019R |
probably damaging |
Het |
Plch1 |
C |
A |
3: 63,628,636 (GRCm39) |
K542N |
probably damaging |
Het |
Plekhj1 |
T |
C |
10: 80,632,471 (GRCm39) |
Q113R |
not run |
Het |
Postn |
A |
T |
3: 54,291,913 (GRCm39) |
I705F |
probably damaging |
Het |
Ppp1r15b |
G |
T |
1: 133,059,352 (GRCm39) |
|
probably benign |
Het |
Prkab1 |
T |
C |
5: 116,159,689 (GRCm39) |
E59G |
probably damaging |
Het |
Qrfprl |
T |
A |
6: 65,433,174 (GRCm39) |
Y331* |
probably null |
Het |
Raph1 |
GG |
GGGGG |
1: 60,528,426 (GRCm39) |
|
probably benign |
Het |
Rassf6 |
AGCAATGGGGATTC |
AGCAATGGGGATTCTGCCTCACTCATGGTCCTGTAGCGCAATGGGGATTC |
5: 90,756,788 (GRCm39) |
|
probably benign |
Het |
Rnf144a |
TCTC |
TCTCTCTCTCTCTCTCACTC |
12: 26,364,013 (GRCm39) |
|
probably benign |
Het |
Ros1 |
T |
A |
10: 52,031,217 (GRCm39) |
M484L |
probably benign |
Het |
Rpa1 |
GCTGCTGCC |
GC |
11: 75,209,343 (GRCm39) |
|
probably null |
Het |
Sectm1b |
A |
G |
11: 120,945,756 (GRCm39) |
V195A |
probably benign |
Het |
Sirpa |
TCATCAG |
T |
2: 129,451,123 (GRCm39) |
|
probably null |
Het |
Slc28a1 |
T |
A |
7: 80,819,032 (GRCm39) |
|
probably null |
Het |
Sphk1 |
G |
C |
11: 116,425,771 (GRCm39) |
S42T |
possibly damaging |
Het |
Spta1 |
T |
C |
1: 174,036,885 (GRCm39) |
L1132P |
probably damaging |
Het |
Srrt |
A |
T |
5: 137,298,262 (GRCm39) |
N303K |
probably benign |
Het |
Ssh2 |
A |
G |
11: 77,344,880 (GRCm39) |
E955G |
probably damaging |
Het |
Strn |
CCAGTC |
CCAGTCCGTGCTCCCTTACCCCAGTCCGTGCTCCCTTACCACAGTC |
17: 78,984,712 (GRCm39) |
|
probably null |
Het |
Tchhl1 |
T |
C |
3: 93,377,691 (GRCm39) |
F132L |
probably benign |
Het |
Tex14 |
A |
G |
11: 87,405,572 (GRCm39) |
E828G |
probably benign |
Het |
Tfeb |
CAG |
CAGGAG |
17: 48,097,020 (GRCm39) |
|
probably benign |
Het |
Tmtc1 |
T |
C |
6: 148,149,009 (GRCm39) |
Y699C |
probably damaging |
Het |
Ubn1 |
A |
G |
16: 4,882,256 (GRCm39) |
Y239C |
probably damaging |
Het |
Vmn2r23 |
T |
G |
6: 123,690,075 (GRCm39) |
L317R |
probably benign |
Het |
Vps72 |
T |
G |
3: 95,028,719 (GRCm39) |
|
probably null |
Het |
Zc3h11a |
A |
G |
1: 133,554,853 (GRCm39) |
S376P |
possibly damaging |
Het |
Zfp384 |
GCCCAGGC |
GCCCAGGCCCAGTCCCAGGC |
6: 125,013,452 (GRCm39) |
|
probably benign |
Het |
Zfp598 |
CAACCAC |
CAACCACAACCAC |
17: 24,899,745 (GRCm39) |
|
probably benign |
Het |
Zfp628 |
TACTCCTCCACCC |
T |
7: 4,923,948 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn2r78 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01302:Vmn2r78
|
APN |
7 |
86,564,569 (GRCm39) |
missense |
unknown |
|
IGL01473:Vmn2r78
|
APN |
7 |
86,569,520 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01767:Vmn2r78
|
APN |
7 |
86,603,643 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02322:Vmn2r78
|
APN |
7 |
86,570,687 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02537:Vmn2r78
|
APN |
7 |
86,603,496 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03297:Vmn2r78
|
APN |
7 |
86,569,969 (GRCm39) |
nonsense |
probably null |
|
ANU74:Vmn2r78
|
UTSW |
7 |
86,570,273 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0035:Vmn2r78
|
UTSW |
7 |
86,569,413 (GRCm39) |
missense |
probably benign |
0.22 |
R0081:Vmn2r78
|
UTSW |
7 |
86,572,235 (GRCm39) |
missense |
probably benign |
0.35 |
R0401:Vmn2r78
|
UTSW |
7 |
86,570,519 (GRCm39) |
missense |
probably benign |
0.04 |
R0751:Vmn2r78
|
UTSW |
7 |
86,603,588 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1341:Vmn2r78
|
UTSW |
7 |
86,571,477 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1386:Vmn2r78
|
UTSW |
7 |
86,564,615 (GRCm39) |
missense |
unknown |
|
R1526:Vmn2r78
|
UTSW |
7 |
86,571,465 (GRCm39) |
splice site |
probably null |
|
R1712:Vmn2r78
|
UTSW |
7 |
86,604,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Vmn2r78
|
UTSW |
7 |
86,569,997 (GRCm39) |
missense |
probably benign |
|
R1812:Vmn2r78
|
UTSW |
7 |
86,569,995 (GRCm39) |
missense |
probably benign |
0.38 |
R2011:Vmn2r78
|
UTSW |
7 |
86,604,287 (GRCm39) |
missense |
possibly damaging |
0.52 |
R2144:Vmn2r78
|
UTSW |
7 |
86,603,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R2197:Vmn2r78
|
UTSW |
7 |
86,570,535 (GRCm39) |
missense |
probably damaging |
0.96 |
R2291:Vmn2r78
|
UTSW |
7 |
86,569,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R2409:Vmn2r78
|
UTSW |
7 |
86,569,953 (GRCm39) |
splice site |
probably benign |
|
R3023:Vmn2r78
|
UTSW |
7 |
86,604,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R4486:Vmn2r78
|
UTSW |
7 |
86,569,959 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4512:Vmn2r78
|
UTSW |
7 |
86,569,452 (GRCm39) |
missense |
probably benign |
0.00 |
R4515:Vmn2r78
|
UTSW |
7 |
86,603,466 (GRCm39) |
missense |
probably damaging |
0.99 |
R4544:Vmn2r78
|
UTSW |
7 |
86,570,399 (GRCm39) |
missense |
probably benign |
|
R4546:Vmn2r78
|
UTSW |
7 |
86,603,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R4872:Vmn2r78
|
UTSW |
7 |
86,603,916 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4928:Vmn2r78
|
UTSW |
7 |
86,603,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R5101:Vmn2r78
|
UTSW |
7 |
86,571,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R5265:Vmn2r78
|
UTSW |
7 |
86,569,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Vmn2r78
|
UTSW |
7 |
86,570,238 (GRCm39) |
missense |
probably damaging |
0.98 |
R5442:Vmn2r78
|
UTSW |
7 |
86,569,330 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5567:Vmn2r78
|
UTSW |
7 |
86,570,737 (GRCm39) |
missense |
probably benign |
0.17 |
R5572:Vmn2r78
|
UTSW |
7 |
86,564,720 (GRCm39) |
missense |
probably benign |
0.01 |
R5636:Vmn2r78
|
UTSW |
7 |
86,603,637 (GRCm39) |
missense |
probably damaging |
0.99 |
R5901:Vmn2r78
|
UTSW |
7 |
86,603,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R5977:Vmn2r78
|
UTSW |
7 |
86,604,115 (GRCm39) |
missense |
probably benign |
0.00 |
R5977:Vmn2r78
|
UTSW |
7 |
86,569,541 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6276:Vmn2r78
|
UTSW |
7 |
86,570,318 (GRCm39) |
missense |
probably benign |
0.00 |
R6386:Vmn2r78
|
UTSW |
7 |
86,571,545 (GRCm39) |
nonsense |
probably null |
|
R6724:Vmn2r78
|
UTSW |
7 |
86,603,466 (GRCm39) |
missense |
probably damaging |
0.99 |
R6852:Vmn2r78
|
UTSW |
7 |
86,603,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R6896:Vmn2r78
|
UTSW |
7 |
86,571,558 (GRCm39) |
missense |
probably benign |
0.10 |
R7385:Vmn2r78
|
UTSW |
7 |
86,571,633 (GRCm39) |
missense |
probably benign |
0.18 |
R7578:Vmn2r78
|
UTSW |
7 |
86,603,552 (GRCm39) |
nonsense |
probably null |
|
R7680:Vmn2r78
|
UTSW |
7 |
86,604,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R7748:Vmn2r78
|
UTSW |
7 |
86,570,343 (GRCm39) |
missense |
probably benign |
0.00 |
R7852:Vmn2r78
|
UTSW |
7 |
86,569,378 (GRCm39) |
nonsense |
probably null |
|
R8031:Vmn2r78
|
UTSW |
7 |
86,604,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R8070:Vmn2r78
|
UTSW |
7 |
86,571,695 (GRCm39) |
missense |
probably benign |
0.01 |
R8085:Vmn2r78
|
UTSW |
7 |
86,603,998 (GRCm39) |
missense |
probably benign |
0.00 |
R8163:Vmn2r78
|
UTSW |
7 |
86,603,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R8501:Vmn2r78
|
UTSW |
7 |
86,570,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R8749:Vmn2r78
|
UTSW |
7 |
86,603,513 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9209:Vmn2r78
|
UTSW |
7 |
86,569,431 (GRCm39) |
missense |
probably benign |
0.08 |
Z1177:Vmn2r78
|
UTSW |
7 |
86,603,982 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Vmn2r78
|
UTSW |
7 |
86,570,415 (GRCm39) |
missense |
probably benign |
0.44 |
|