Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam5 |
G |
A |
8: 25,296,517 (GRCm39) |
S310L |
probably damaging |
Het |
Adamts16 |
C |
T |
13: 70,946,157 (GRCm39) |
|
probably null |
Het |
Arrb1 |
C |
A |
7: 99,240,569 (GRCm39) |
D194E |
probably benign |
Het |
Atp1a3 |
T |
C |
7: 24,697,051 (GRCm39) |
D217G |
probably damaging |
Het |
Bcar3 |
A |
G |
3: 122,302,033 (GRCm39) |
I123V |
possibly damaging |
Het |
Bdp1 |
G |
A |
13: 100,180,321 (GRCm39) |
L1833F |
probably damaging |
Het |
Cdc14a |
T |
C |
3: 116,122,355 (GRCm39) |
Y155C |
probably damaging |
Het |
Cdo1 |
C |
A |
18: 46,853,380 (GRCm39) |
R126M |
possibly damaging |
Het |
Cfap99 |
G |
T |
5: 34,484,604 (GRCm39) |
R627L |
probably damaging |
Het |
Efr3a |
T |
A |
15: 65,720,030 (GRCm39) |
L369* |
probably null |
Het |
Erich6 |
A |
C |
3: 58,543,516 (GRCm39) |
F185V |
probably damaging |
Het |
Fank1 |
A |
G |
7: 133,478,627 (GRCm39) |
I230M |
possibly damaging |
Het |
Flg2 |
A |
T |
3: 93,109,977 (GRCm39) |
E668D |
unknown |
Het |
Flg2 |
A |
C |
3: 93,110,256 (GRCm39) |
R761S |
unknown |
Het |
Gabrr1 |
T |
C |
4: 33,158,157 (GRCm39) |
L260P |
probably damaging |
Het |
Gfm2 |
G |
A |
13: 97,285,868 (GRCm39) |
R119K |
probably damaging |
Het |
Gm14226 |
A |
G |
2: 154,866,357 (GRCm39) |
T105A |
probably benign |
Het |
Gm14496 |
A |
G |
2: 181,637,997 (GRCm39) |
N357S |
probably damaging |
Het |
Gm5916 |
G |
A |
9: 36,039,935 (GRCm39) |
L18F |
probably benign |
Het |
Golm1 |
A |
T |
13: 59,790,058 (GRCm39) |
N247K |
probably benign |
Het |
Gpatch2l |
G |
A |
12: 86,290,958 (GRCm39) |
R47H |
probably damaging |
Het |
Greb1 |
C |
T |
12: 16,773,355 (GRCm39) |
A240T |
probably benign |
Het |
Gtf3c6 |
T |
C |
10: 40,125,774 (GRCm39) |
M148V |
probably benign |
Het |
Guca1a |
T |
C |
17: 47,706,102 (GRCm39) |
S126G |
probably benign |
Het |
Hacl1 |
A |
T |
14: 31,337,380 (GRCm39) |
I393N |
possibly damaging |
Het |
Hddc3 |
A |
G |
7: 79,993,498 (GRCm39) |
D68G |
possibly damaging |
Het |
Hsfy2 |
T |
C |
1: 56,675,569 (GRCm39) |
T323A |
possibly damaging |
Het |
Kcng2 |
T |
C |
18: 80,366,358 (GRCm39) |
|
probably benign |
Het |
Kdm2a |
G |
T |
19: 4,395,669 (GRCm39) |
P321T |
probably benign |
Het |
Krt31 |
A |
G |
11: 99,938,558 (GRCm39) |
V345A |
probably benign |
Het |
Lrrc37 |
A |
T |
11: 103,509,583 (GRCm39) |
L795* |
probably null |
Het |
Mettl1 |
T |
C |
10: 126,880,887 (GRCm39) |
S193P |
probably benign |
Het |
Mme |
G |
A |
3: 63,253,523 (GRCm39) |
D456N |
possibly damaging |
Het |
Mmrn1 |
A |
G |
6: 60,954,367 (GRCm39) |
T883A |
probably benign |
Het |
Mphosph10 |
C |
G |
7: 64,038,669 (GRCm39) |
E293Q |
probably benign |
Het |
Muc16 |
C |
A |
9: 18,557,193 (GRCm39) |
K3033N |
unknown |
Het |
Myo16 |
C |
T |
8: 10,619,496 (GRCm39) |
T1349M |
probably damaging |
Het |
Myo5c |
T |
C |
9: 75,157,746 (GRCm39) |
I233T |
probably benign |
Het |
Or4p4b-ps1 |
A |
G |
2: 88,454,189 (GRCm39) |
T181A |
unknown |
Het |
Or52a33 |
T |
G |
7: 103,289,065 (GRCm39) |
N94T |
probably benign |
Het |
Or52ac1 |
A |
T |
7: 104,246,018 (GRCm39) |
F123L |
probably benign |
Het |
Or5b111 |
A |
T |
19: 13,291,036 (GRCm39) |
S204R |
probably benign |
Het |
Or5h22 |
A |
G |
16: 58,894,555 (GRCm39) |
M296T |
probably benign |
Het |
Or6c2 |
T |
A |
10: 129,362,732 (GRCm39) |
V212E |
probably damaging |
Het |
Or7c70 |
C |
A |
10: 78,683,351 (GRCm39) |
V133L |
probably benign |
Het |
Oxct2b |
A |
G |
4: 123,011,480 (GRCm39) |
I467V |
probably benign |
Het |
Parp1 |
A |
T |
1: 180,414,936 (GRCm39) |
N425Y |
possibly damaging |
Het |
Pcdhgc3 |
T |
A |
18: 37,939,656 (GRCm39) |
V19D |
possibly damaging |
Het |
Pfkl |
T |
A |
10: 77,833,423 (GRCm39) |
I260F |
probably damaging |
Het |
Pkd1l1 |
C |
T |
11: 8,799,046 (GRCm39) |
G1789R |
probably damaging |
Het |
Pla1a |
G |
A |
16: 38,217,830 (GRCm39) |
A386V |
probably benign |
Het |
Pml |
A |
G |
9: 58,142,169 (GRCm39) |
L221P |
probably damaging |
Het |
Rcn2 |
C |
T |
9: 55,964,845 (GRCm39) |
Q268* |
probably null |
Het |
Reps1 |
T |
A |
10: 17,969,603 (GRCm39) |
D235E |
probably damaging |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGGCGGCGG |
7: 97,229,118 (GRCm39) |
|
probably benign |
Het |
Sap30bp |
A |
G |
11: 115,824,314 (GRCm39) |
|
probably benign |
Het |
Scn1a |
A |
T |
2: 66,118,075 (GRCm39) |
S1433T |
probably damaging |
Het |
Sde2 |
T |
C |
1: 180,678,754 (GRCm39) |
V6A |
probably benign |
Het |
Sdk1 |
C |
A |
5: 142,197,769 (GRCm39) |
R2141S |
probably benign |
Het |
Setd2 |
T |
C |
9: 110,379,640 (GRCm39) |
S1152P |
probably damaging |
Het |
Slc26a2 |
C |
T |
18: 61,334,926 (GRCm39) |
V176I |
probably damaging |
Het |
Snx7 |
A |
G |
3: 117,640,281 (GRCm39) |
I76T |
possibly damaging |
Het |
Specc1l |
C |
A |
10: 75,082,113 (GRCm39) |
A520D |
probably benign |
Het |
Spop |
A |
G |
11: 95,362,136 (GRCm39) |
T56A |
possibly damaging |
Het |
Syne2 |
T |
A |
12: 76,074,786 (GRCm39) |
D4576E |
probably damaging |
Het |
Tas2r134 |
A |
C |
2: 51,517,601 (GRCm39) |
M27L |
probably benign |
Het |
Tecta |
A |
C |
9: 42,278,082 (GRCm39) |
I1142S |
probably benign |
Het |
Timm44 |
T |
C |
8: 4,316,611 (GRCm39) |
D311G |
possibly damaging |
Het |
Tmem123 |
C |
G |
9: 7,791,071 (GRCm39) |
T124R |
possibly damaging |
Het |
Tmem184b |
A |
T |
15: 79,246,959 (GRCm39) |
L370Q |
probably benign |
Het |
Trim25 |
T |
A |
11: 88,890,329 (GRCm39) |
N5K |
probably benign |
Het |
Vmn2r93 |
A |
G |
17: 18,524,903 (GRCm39) |
Y187C |
probably damaging |
Het |
Vpreb1a |
A |
G |
16: 16,686,678 (GRCm39) |
Y71H |
probably damaging |
Het |
Vpreb1b |
T |
C |
16: 17,798,441 (GRCm39) |
S5P |
probably benign |
Het |
Xpo7 |
A |
T |
14: 70,906,888 (GRCm39) |
C939S |
probably benign |
Het |
Zfp78 |
C |
A |
7: 6,381,764 (GRCm39) |
S271R |
probably benign |
Het |
Zic5 |
A |
T |
14: 122,702,080 (GRCm39) |
M217K |
probably benign |
Het |
|
Other mutations in Fam186a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00588:Fam186a
|
APN |
15 |
99,825,572 (GRCm39) |
splice site |
probably benign |
|
IGL03047:Fam186a
|
UTSW |
15 |
99,843,589 (GRCm39) |
missense |
unknown |
|
R0172:Fam186a
|
UTSW |
15 |
99,852,768 (GRCm39) |
missense |
unknown |
|
R0194:Fam186a
|
UTSW |
15 |
99,839,644 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0381:Fam186a
|
UTSW |
15 |
99,840,055 (GRCm39) |
missense |
probably damaging |
0.97 |
R0799:Fam186a
|
UTSW |
15 |
99,839,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Fam186a
|
UTSW |
15 |
99,837,670 (GRCm39) |
splice site |
probably benign |
|
R1366:Fam186a
|
UTSW |
15 |
99,841,270 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1519:Fam186a
|
UTSW |
15 |
99,845,536 (GRCm39) |
missense |
unknown |
|
R1592:Fam186a
|
UTSW |
15 |
99,838,199 (GRCm39) |
missense |
probably benign |
0.01 |
R1636:Fam186a
|
UTSW |
15 |
99,839,539 (GRCm39) |
missense |
unknown |
|
R1719:Fam186a
|
UTSW |
15 |
99,840,227 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1759:Fam186a
|
UTSW |
15 |
99,864,762 (GRCm39) |
nonsense |
probably null |
|
R1856:Fam186a
|
UTSW |
15 |
99,838,183 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2131:Fam186a
|
UTSW |
15 |
99,831,557 (GRCm39) |
unclassified |
probably benign |
|
R2192:Fam186a
|
UTSW |
15 |
99,838,192 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2239:Fam186a
|
UTSW |
15 |
99,852,745 (GRCm39) |
missense |
unknown |
|
R2251:Fam186a
|
UTSW |
15 |
99,842,978 (GRCm39) |
missense |
probably benign |
0.02 |
R2902:Fam186a
|
UTSW |
15 |
99,843,049 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3037:Fam186a
|
UTSW |
15 |
99,841,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R3744:Fam186a
|
UTSW |
15 |
99,845,416 (GRCm39) |
missense |
unknown |
|
R4021:Fam186a
|
UTSW |
15 |
99,839,680 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4183:Fam186a
|
UTSW |
15 |
99,831,566 (GRCm39) |
unclassified |
probably benign |
|
R4238:Fam186a
|
UTSW |
15 |
99,841,523 (GRCm39) |
missense |
probably benign |
0.05 |
R4667:Fam186a
|
UTSW |
15 |
99,842,413 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4817:Fam186a
|
UTSW |
15 |
99,831,419 (GRCm39) |
unclassified |
probably benign |
|
R4835:Fam186a
|
UTSW |
15 |
99,843,689 (GRCm39) |
missense |
unknown |
|
R4837:Fam186a
|
UTSW |
15 |
99,838,678 (GRCm39) |
missense |
unknown |
|
R4897:Fam186a
|
UTSW |
15 |
99,843,158 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4902:Fam186a
|
UTSW |
15 |
99,844,723 (GRCm39) |
missense |
unknown |
|
R4950:Fam186a
|
UTSW |
15 |
99,839,534 (GRCm39) |
missense |
unknown |
|
R4995:Fam186a
|
UTSW |
15 |
99,842,980 (GRCm39) |
missense |
probably benign |
0.27 |
R5062:Fam186a
|
UTSW |
15 |
99,842,527 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5124:Fam186a
|
UTSW |
15 |
99,840,977 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5133:Fam186a
|
UTSW |
15 |
99,853,374 (GRCm39) |
missense |
unknown |
|
R5424:Fam186a
|
UTSW |
15 |
99,843,644 (GRCm39) |
missense |
unknown |
|
R5624:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5628:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5637:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5639:Fam186a
|
UTSW |
15 |
99,844,931 (GRCm39) |
missense |
unknown |
|
R5652:Fam186a
|
UTSW |
15 |
99,843,253 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5673:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5799:Fam186a
|
UTSW |
15 |
99,864,705 (GRCm39) |
nonsense |
probably null |
|
R5965:Fam186a
|
UTSW |
15 |
99,842,978 (GRCm39) |
missense |
probably benign |
0.37 |
R6044:Fam186a
|
UTSW |
15 |
99,839,878 (GRCm39) |
missense |
probably damaging |
0.97 |
R6077:Fam186a
|
UTSW |
15 |
99,840,584 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6120:Fam186a
|
UTSW |
15 |
99,838,244 (GRCm39) |
missense |
probably benign |
0.00 |
R6185:Fam186a
|
UTSW |
15 |
99,845,530 (GRCm39) |
missense |
unknown |
|
R6186:Fam186a
|
UTSW |
15 |
99,845,206 (GRCm39) |
missense |
unknown |
|
R6242:Fam186a
|
UTSW |
15 |
99,837,788 (GRCm39) |
missense |
unknown |
|
R6351:Fam186a
|
UTSW |
15 |
99,839,623 (GRCm39) |
missense |
probably damaging |
0.97 |
R6368:Fam186a
|
UTSW |
15 |
99,841,198 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6369:Fam186a
|
UTSW |
15 |
99,845,212 (GRCm39) |
missense |
unknown |
|
R6559:Fam186a
|
UTSW |
15 |
99,842,356 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6855:Fam186a
|
UTSW |
15 |
99,852,756 (GRCm39) |
missense |
unknown |
|
R6867:Fam186a
|
UTSW |
15 |
99,843,731 (GRCm39) |
missense |
unknown |
|
R6957:Fam186a
|
UTSW |
15 |
99,844,357 (GRCm39) |
missense |
unknown |
|
R6961:Fam186a
|
UTSW |
15 |
99,838,082 (GRCm39) |
missense |
probably benign |
0.16 |
R6994:Fam186a
|
UTSW |
15 |
99,840,347 (GRCm39) |
missense |
probably benign |
0.35 |
R7062:Fam186a
|
UTSW |
15 |
99,831,521 (GRCm39) |
unclassified |
probably benign |
|
R7064:Fam186a
|
UTSW |
15 |
99,839,557 (GRCm39) |
missense |
unknown |
|
R7173:Fam186a
|
UTSW |
15 |
99,843,531 (GRCm39) |
missense |
unknown |
|
R7244:Fam186a
|
UTSW |
15 |
99,844,273 (GRCm39) |
missense |
unknown |
|
R7270:Fam186a
|
UTSW |
15 |
99,842,033 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7410:Fam186a
|
UTSW |
15 |
99,844,826 (GRCm39) |
nonsense |
probably null |
|
R7437:Fam186a
|
UTSW |
15 |
99,840,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Fam186a
|
UTSW |
15 |
99,845,395 (GRCm39) |
missense |
unknown |
|
R7487:Fam186a
|
UTSW |
15 |
99,840,017 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7526:Fam186a
|
UTSW |
15 |
99,839,796 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7650:Fam186a
|
UTSW |
15 |
99,837,788 (GRCm39) |
missense |
unknown |
|
R7658:Fam186a
|
UTSW |
15 |
99,837,725 (GRCm39) |
missense |
unknown |
|
R7663:Fam186a
|
UTSW |
15 |
99,842,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7703:Fam186a
|
UTSW |
15 |
99,852,678 (GRCm39) |
missense |
unknown |
|
R7814:Fam186a
|
UTSW |
15 |
99,842,545 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7958:Fam186a
|
UTSW |
15 |
99,841,189 (GRCm39) |
missense |
probably damaging |
0.99 |
R7970:Fam186a
|
UTSW |
15 |
99,831,467 (GRCm39) |
missense |
unknown |
|
R8076:Fam186a
|
UTSW |
15 |
99,841,351 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8087:Fam186a
|
UTSW |
15 |
99,839,725 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8130:Fam186a
|
UTSW |
15 |
99,841,914 (GRCm39) |
frame shift |
probably null |
|
R8239:Fam186a
|
UTSW |
15 |
99,839,191 (GRCm39) |
missense |
unknown |
|
R8246:Fam186a
|
UTSW |
15 |
99,838,428 (GRCm39) |
missense |
unknown |
|
R8446:Fam186a
|
UTSW |
15 |
99,845,335 (GRCm39) |
missense |
unknown |
|
R8469:Fam186a
|
UTSW |
15 |
99,845,186 (GRCm39) |
missense |
unknown |
|
R8676:Fam186a
|
UTSW |
15 |
99,845,023 (GRCm39) |
missense |
unknown |
|
R8790:Fam186a
|
UTSW |
15 |
99,841,024 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8808:Fam186a
|
UTSW |
15 |
99,842,604 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8848:Fam186a
|
UTSW |
15 |
99,838,034 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9083:Fam186a
|
UTSW |
15 |
99,843,079 (GRCm39) |
missense |
probably benign |
0.27 |
R9106:Fam186a
|
UTSW |
15 |
99,844,107 (GRCm39) |
small deletion |
probably benign |
|
R9116:Fam186a
|
UTSW |
15 |
99,840,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9156:Fam186a
|
UTSW |
15 |
99,841,159 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9227:Fam186a
|
UTSW |
15 |
99,853,384 (GRCm39) |
missense |
unknown |
|
R9250:Fam186a
|
UTSW |
15 |
99,845,330 (GRCm39) |
missense |
unknown |
|
R9282:Fam186a
|
UTSW |
15 |
99,839,879 (GRCm39) |
missense |
probably damaging |
0.97 |
R9495:Fam186a
|
UTSW |
15 |
99,844,766 (GRCm39) |
missense |
unknown |
|
R9514:Fam186a
|
UTSW |
15 |
99,844,766 (GRCm39) |
missense |
unknown |
|
R9521:Fam186a
|
UTSW |
15 |
99,841,471 (GRCm39) |
missense |
probably damaging |
0.97 |
R9553:Fam186a
|
UTSW |
15 |
99,844,561 (GRCm39) |
missense |
unknown |
|
R9641:Fam186a
|
UTSW |
15 |
99,838,244 (GRCm39) |
missense |
probably benign |
0.00 |
R9655:Fam186a
|
UTSW |
15 |
99,840,973 (GRCm39) |
missense |
probably damaging |
0.99 |
R9661:Fam186a
|
UTSW |
15 |
99,842,492 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9673:Fam186a
|
UTSW |
15 |
99,841,024 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9762:Fam186a
|
UTSW |
15 |
99,842,393 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0021:Fam186a
|
UTSW |
15 |
99,843,316 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Fam186a
|
UTSW |
15 |
99,843,875 (GRCm39) |
missense |
unknown |
|
|