Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5530400C23Rik |
A |
G |
6: 133,271,082 (GRCm39) |
Q42R |
probably benign |
Het |
Acaa1a |
A |
G |
9: 119,178,556 (GRCm39) |
|
probably null |
Het |
Agbl5 |
T |
C |
5: 31,062,067 (GRCm39) |
S756P |
probably damaging |
Het |
Armc9 |
T |
C |
1: 86,122,060 (GRCm39) |
L395P |
probably damaging |
Het |
Cdc16 |
C |
T |
8: 13,819,489 (GRCm39) |
Q362* |
probably null |
Het |
Cdh5 |
C |
T |
8: 104,856,002 (GRCm39) |
R312C |
probably damaging |
Het |
Cep170b |
C |
T |
12: 112,704,902 (GRCm39) |
Q887* |
probably null |
Het |
Chd9 |
T |
C |
8: 91,763,219 (GRCm39) |
I2348T |
probably damaging |
Het |
Clec9a |
A |
G |
6: 129,398,001 (GRCm39) |
|
probably benign |
Het |
Col6a3 |
T |
C |
1: 90,731,813 (GRCm39) |
D873G |
probably benign |
Het |
D130040H23Rik |
T |
C |
8: 69,755,579 (GRCm39) |
I328T |
probably benign |
Het |
Dido1 |
G |
T |
2: 180,302,728 (GRCm39) |
D1725E |
possibly damaging |
Het |
Dnajb14 |
A |
G |
3: 137,598,631 (GRCm39) |
D123G |
probably null |
Het |
Dock2 |
A |
T |
11: 34,580,587 (GRCm39) |
M661K |
probably damaging |
Het |
Esam |
C |
T |
9: 37,448,426 (GRCm39) |
|
probably null |
Het |
Fam20c |
A |
T |
5: 138,743,623 (GRCm39) |
N220Y |
probably damaging |
Het |
Fat2 |
G |
T |
11: 55,169,824 (GRCm39) |
H2978Q |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,162,846 (GRCm39) |
T2147A |
possibly damaging |
Het |
Fdft1 |
T |
C |
14: 63,394,070 (GRCm39) |
T214A |
probably damaging |
Het |
Fhl5 |
T |
C |
4: 25,211,252 (GRCm39) |
S147G |
probably benign |
Het |
Flrt2 |
A |
G |
12: 95,747,378 (GRCm39) |
Y572C |
probably damaging |
Het |
Gcat |
A |
T |
15: 78,926,297 (GRCm39) |
T56S |
possibly damaging |
Het |
Gemin5 |
A |
T |
11: 58,047,454 (GRCm39) |
|
probably null |
Het |
Gm4736 |
A |
T |
6: 132,092,640 (GRCm39) |
|
noncoding transcript |
Het |
Grin2b |
T |
C |
6: 135,820,108 (GRCm39) |
N368S |
probably benign |
Het |
Gsto1 |
T |
C |
19: 47,846,344 (GRCm39) |
F64L |
probably benign |
Het |
Gucy1a1 |
A |
G |
3: 82,013,440 (GRCm39) |
S401P |
probably damaging |
Het |
Htr1f |
G |
A |
16: 64,746,260 (GRCm39) |
P344L |
probably damaging |
Het |
Ighv7-3 |
T |
A |
12: 114,116,919 (GRCm39) |
Y81F |
probably damaging |
Het |
Jakmip3 |
C |
A |
7: 138,619,474 (GRCm39) |
|
probably benign |
Het |
Kcnj13 |
T |
C |
1: 87,314,641 (GRCm39) |
T194A |
probably benign |
Het |
Khdrbs3 |
T |
C |
15: 68,921,224 (GRCm39) |
|
probably benign |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Lyn |
A |
T |
4: 3,746,833 (GRCm39) |
I204F |
probably damaging |
Het |
Mbd6 |
C |
G |
10: 127,122,372 (GRCm39) |
R152P |
probably null |
Het |
Myof |
A |
G |
19: 37,911,426 (GRCm39) |
S1502P |
probably damaging |
Het |
Myom2 |
T |
G |
8: 15,135,294 (GRCm39) |
I499S |
probably benign |
Het |
Nos2 |
T |
A |
11: 78,850,521 (GRCm39) |
F1126L |
possibly damaging |
Het |
Or3a4 |
G |
A |
11: 73,944,814 (GRCm39) |
T257I |
probably damaging |
Het |
P2ry1 |
T |
C |
3: 60,911,133 (GRCm39) |
F91L |
probably damaging |
Het |
Pcdh15 |
C |
A |
10: 74,420,054 (GRCm39) |
D1166E |
probably benign |
Het |
Pou6f1 |
C |
A |
15: 100,478,805 (GRCm39) |
V368L |
probably benign |
Het |
Ptcd3 |
A |
T |
6: 71,860,470 (GRCm39) |
I579K |
possibly damaging |
Het |
Rbm45 |
A |
G |
2: 76,209,362 (GRCm39) |
E392G |
probably damaging |
Het |
Rnf168 |
A |
G |
16: 32,118,010 (GRCm39) |
N524D |
probably benign |
Het |
Rnf222 |
G |
T |
11: 68,783,982 (GRCm39) |
R183L |
probably damaging |
Het |
Robo1 |
C |
T |
16: 72,832,805 (GRCm39) |
T1526I |
probably benign |
Het |
Sel1l |
A |
G |
12: 91,776,776 (GRCm39) |
W689R |
probably damaging |
Het |
Serpinb13 |
T |
C |
1: 106,926,657 (GRCm39) |
S218P |
probably damaging |
Het |
Serpini1 |
A |
G |
3: 75,547,589 (GRCm39) |
Y367C |
probably damaging |
Het |
Slc13a2 |
A |
G |
11: 78,291,666 (GRCm39) |
F329S |
probably benign |
Het |
Smc2 |
T |
C |
4: 52,476,850 (GRCm39) |
|
probably benign |
Het |
Tab2 |
G |
A |
10: 7,783,245 (GRCm39) |
P679L |
probably damaging |
Het |
Tdrd1 |
T |
A |
19: 56,819,663 (GRCm39) |
N54K |
possibly damaging |
Het |
Tgfbr2 |
T |
C |
9: 115,958,901 (GRCm39) |
Y146C |
probably damaging |
Het |
Tnfrsf11a |
A |
G |
1: 105,737,130 (GRCm39) |
D79G |
possibly damaging |
Het |
Trpa1 |
T |
C |
1: 14,944,605 (GRCm39) |
I1046M |
probably benign |
Het |
Ubn1 |
A |
G |
16: 4,892,243 (GRCm39) |
|
probably benign |
Het |
Ubp1 |
T |
C |
9: 113,780,754 (GRCm39) |
|
probably null |
Het |
Vmn2r2 |
A |
T |
3: 64,024,320 (GRCm39) |
F754I |
probably benign |
Het |
|
Other mutations in Sycp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00484:Sycp2
|
APN |
2 |
178,024,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00578:Sycp2
|
APN |
2 |
177,992,615 (GRCm39) |
splice site |
probably benign |
|
IGL00646:Sycp2
|
APN |
2 |
178,016,252 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01309:Sycp2
|
APN |
2 |
177,999,904 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01464:Sycp2
|
APN |
2 |
178,043,425 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01539:Sycp2
|
APN |
2 |
178,016,488 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01670:Sycp2
|
APN |
2 |
178,019,843 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02138:Sycp2
|
APN |
2 |
178,043,783 (GRCm39) |
nonsense |
probably null |
|
IGL02138:Sycp2
|
APN |
2 |
178,000,047 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02630:Sycp2
|
APN |
2 |
178,043,712 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02673:Sycp2
|
APN |
2 |
178,036,004 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02961:Sycp2
|
APN |
2 |
178,022,655 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03084:Sycp2
|
APN |
2 |
178,033,584 (GRCm39) |
unclassified |
probably benign |
|
IGL03123:Sycp2
|
APN |
2 |
177,994,272 (GRCm39) |
nonsense |
probably null |
|
IGL03167:Sycp2
|
APN |
2 |
178,021,291 (GRCm39) |
missense |
probably damaging |
0.99 |
R0043:Sycp2
|
UTSW |
2 |
178,006,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R0050:Sycp2
|
UTSW |
2 |
178,006,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Sycp2
|
UTSW |
2 |
178,045,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R0096:Sycp2
|
UTSW |
2 |
178,045,528 (GRCm39) |
missense |
probably damaging |
0.99 |
R0310:Sycp2
|
UTSW |
2 |
178,023,648 (GRCm39) |
missense |
probably benign |
0.44 |
R0363:Sycp2
|
UTSW |
2 |
177,988,204 (GRCm39) |
splice site |
probably benign |
|
R0456:Sycp2
|
UTSW |
2 |
178,023,648 (GRCm39) |
missense |
probably benign |
0.44 |
R0597:Sycp2
|
UTSW |
2 |
177,998,373 (GRCm39) |
missense |
possibly damaging |
0.54 |
R0608:Sycp2
|
UTSW |
2 |
178,024,197 (GRCm39) |
missense |
probably damaging |
0.98 |
R1112:Sycp2
|
UTSW |
2 |
177,994,329 (GRCm39) |
missense |
probably benign |
0.05 |
R1127:Sycp2
|
UTSW |
2 |
178,016,159 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1208:Sycp2
|
UTSW |
2 |
177,998,421 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1208:Sycp2
|
UTSW |
2 |
177,998,421 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1323:Sycp2
|
UTSW |
2 |
177,989,414 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1323:Sycp2
|
UTSW |
2 |
177,989,414 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1413:Sycp2
|
UTSW |
2 |
177,989,590 (GRCm39) |
missense |
probably benign |
0.00 |
R1557:Sycp2
|
UTSW |
2 |
178,037,009 (GRCm39) |
unclassified |
probably benign |
|
R1562:Sycp2
|
UTSW |
2 |
178,024,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Sycp2
|
UTSW |
2 |
177,993,461 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1932:Sycp2
|
UTSW |
2 |
178,023,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R1950:Sycp2
|
UTSW |
2 |
178,044,593 (GRCm39) |
missense |
probably benign |
0.00 |
R2001:Sycp2
|
UTSW |
2 |
178,019,848 (GRCm39) |
missense |
probably benign |
0.05 |
R2105:Sycp2
|
UTSW |
2 |
177,991,931 (GRCm39) |
splice site |
probably null |
|
R2382:Sycp2
|
UTSW |
2 |
178,019,811 (GRCm39) |
critical splice donor site |
probably null |
|
R2403:Sycp2
|
UTSW |
2 |
178,045,528 (GRCm39) |
nonsense |
probably null |
|
R2483:Sycp2
|
UTSW |
2 |
178,016,388 (GRCm39) |
missense |
probably damaging |
0.98 |
R3003:Sycp2
|
UTSW |
2 |
177,999,916 (GRCm39) |
missense |
probably benign |
0.01 |
R3686:Sycp2
|
UTSW |
2 |
178,016,177 (GRCm39) |
missense |
probably benign |
0.16 |
R4038:Sycp2
|
UTSW |
2 |
178,022,720 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4039:Sycp2
|
UTSW |
2 |
178,022,720 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4272:Sycp2
|
UTSW |
2 |
178,000,017 (GRCm39) |
missense |
probably benign |
0.04 |
R4343:Sycp2
|
UTSW |
2 |
178,022,740 (GRCm39) |
missense |
probably damaging |
0.99 |
R4491:Sycp2
|
UTSW |
2 |
178,016,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R4534:Sycp2
|
UTSW |
2 |
177,996,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R4720:Sycp2
|
UTSW |
2 |
178,016,225 (GRCm39) |
missense |
probably benign |
0.11 |
R4805:Sycp2
|
UTSW |
2 |
178,035,754 (GRCm39) |
unclassified |
probably benign |
|
R4807:Sycp2
|
UTSW |
2 |
178,035,754 (GRCm39) |
unclassified |
probably benign |
|
R4808:Sycp2
|
UTSW |
2 |
178,035,754 (GRCm39) |
unclassified |
probably benign |
|
R4906:Sycp2
|
UTSW |
2 |
178,045,450 (GRCm39) |
critical splice donor site |
probably null |
|
R4910:Sycp2
|
UTSW |
2 |
178,000,017 (GRCm39) |
missense |
probably benign |
0.04 |
R5282:Sycp2
|
UTSW |
2 |
178,045,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R5285:Sycp2
|
UTSW |
2 |
178,034,191 (GRCm39) |
splice site |
probably null |
|
R5316:Sycp2
|
UTSW |
2 |
177,998,296 (GRCm39) |
missense |
probably benign |
0.00 |
R5389:Sycp2
|
UTSW |
2 |
178,019,495 (GRCm39) |
splice site |
probably null |
|
R5621:Sycp2
|
UTSW |
2 |
178,023,711 (GRCm39) |
missense |
probably benign |
0.05 |
R5652:Sycp2
|
UTSW |
2 |
178,000,498 (GRCm39) |
splice site |
probably null |
|
R5880:Sycp2
|
UTSW |
2 |
178,016,263 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6114:Sycp2
|
UTSW |
2 |
177,990,038 (GRCm39) |
missense |
probably benign |
0.25 |
R6115:Sycp2
|
UTSW |
2 |
177,990,038 (GRCm39) |
missense |
probably benign |
0.25 |
R6186:Sycp2
|
UTSW |
2 |
178,025,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R6351:Sycp2
|
UTSW |
2 |
178,005,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R6509:Sycp2
|
UTSW |
2 |
178,037,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R6536:Sycp2
|
UTSW |
2 |
177,993,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R6679:Sycp2
|
UTSW |
2 |
178,022,721 (GRCm39) |
missense |
probably damaging |
0.96 |
R6687:Sycp2
|
UTSW |
2 |
177,996,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R6761:Sycp2
|
UTSW |
2 |
178,016,144 (GRCm39) |
splice site |
probably null |
|
R6786:Sycp2
|
UTSW |
2 |
178,025,345 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7357:Sycp2
|
UTSW |
2 |
178,045,597 (GRCm39) |
splice site |
probably null |
|
R7422:Sycp2
|
UTSW |
2 |
178,035,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R7519:Sycp2
|
UTSW |
2 |
177,988,126 (GRCm39) |
makesense |
probably null |
|
R7805:Sycp2
|
UTSW |
2 |
178,022,651 (GRCm39) |
missense |
probably damaging |
0.99 |
R7960:Sycp2
|
UTSW |
2 |
178,046,453 (GRCm39) |
missense |
probably null |
0.90 |
R8022:Sycp2
|
UTSW |
2 |
177,996,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R8037:Sycp2
|
UTSW |
2 |
178,045,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R8038:Sycp2
|
UTSW |
2 |
178,045,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R8039:Sycp2
|
UTSW |
2 |
178,016,378 (GRCm39) |
missense |
probably benign |
0.05 |
R8159:Sycp2
|
UTSW |
2 |
177,996,770 (GRCm39) |
missense |
probably damaging |
0.97 |
R8233:Sycp2
|
UTSW |
2 |
177,998,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R8436:Sycp2
|
UTSW |
2 |
178,004,761 (GRCm39) |
missense |
probably benign |
0.44 |
R8437:Sycp2
|
UTSW |
2 |
178,006,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R8528:Sycp2
|
UTSW |
2 |
178,016,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R8679:Sycp2
|
UTSW |
2 |
177,992,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R8711:Sycp2
|
UTSW |
2 |
177,990,088 (GRCm39) |
missense |
probably benign |
0.41 |
R8843:Sycp2
|
UTSW |
2 |
177,990,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R9044:Sycp2
|
UTSW |
2 |
177,989,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R9067:Sycp2
|
UTSW |
2 |
177,989,214 (GRCm39) |
critical splice donor site |
probably null |
|
R9203:Sycp2
|
UTSW |
2 |
177,996,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R9263:Sycp2
|
UTSW |
2 |
178,035,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R9301:Sycp2
|
UTSW |
2 |
178,023,650 (GRCm39) |
missense |
probably benign |
0.00 |
R9596:Sycp2
|
UTSW |
2 |
177,990,212 (GRCm39) |
critical splice donor site |
probably null |
|
R9633:Sycp2
|
UTSW |
2 |
177,998,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R9715:Sycp2
|
UTSW |
2 |
178,035,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R9748:Sycp2
|
UTSW |
2 |
178,025,304 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Sycp2
|
UTSW |
2 |
178,023,727 (GRCm39) |
missense |
probably benign |
0.17 |
Z1088:Sycp2
|
UTSW |
2 |
178,016,160 (GRCm39) |
missense |
probably benign |
|
Z1176:Sycp2
|
UTSW |
2 |
178,006,674 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sycp2
|
UTSW |
2 |
178,022,668 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1191:Sycp2
|
UTSW |
2 |
177,992,662 (GRCm39) |
missense |
probably benign |
|
|