Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
T |
C |
6: 142,573,245 (GRCm39) |
N1051D |
possibly damaging |
Het |
Abcc9 |
A |
G |
6: 142,536,222 (GRCm39) |
V1504A |
probably damaging |
Het |
Actr6 |
A |
T |
10: 89,564,019 (GRCm39) |
Y84* |
probably null |
Het |
Adgrl3 |
T |
C |
5: 81,841,366 (GRCm39) |
Y816H |
probably damaging |
Het |
Ahcyl2 |
T |
C |
6: 29,768,586 (GRCm39) |
|
probably benign |
Het |
Amd1 |
A |
T |
10: 40,166,404 (GRCm39) |
C157* |
probably null |
Het |
Ank1 |
G |
A |
8: 23,609,393 (GRCm39) |
E1362K |
probably damaging |
Het |
Atp10b |
A |
G |
11: 43,121,391 (GRCm39) |
Q1018R |
probably benign |
Het |
Atp1a2 |
G |
A |
1: 172,106,911 (GRCm39) |
T803I |
probably damaging |
Het |
Atr |
T |
G |
9: 95,814,495 (GRCm39) |
L2064R |
probably damaging |
Het |
Bmp3 |
T |
A |
5: 99,020,264 (GRCm39) |
L229Q |
probably damaging |
Het |
Ccl25 |
A |
G |
8: 4,403,892 (GRCm39) |
*54W |
probably null |
Het |
Cdc45 |
A |
T |
16: 18,627,491 (GRCm39) |
N111K |
possibly damaging |
Het |
Cfap61 |
T |
A |
2: 145,805,363 (GRCm39) |
S154T |
probably benign |
Het |
Cyp2c37 |
T |
A |
19: 39,982,542 (GRCm39) |
S127T |
probably benign |
Het |
Cyp4f40 |
T |
A |
17: 32,892,913 (GRCm39) |
D309E |
probably benign |
Het |
D6Ertd527e |
A |
G |
6: 87,088,335 (GRCm39) |
D166G |
unknown |
Het |
Dmbt1 |
T |
A |
7: 130,651,944 (GRCm39) |
D395E |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,370,555 (GRCm39) |
S2832G |
probably benign |
Het |
Dync1h1 |
G |
A |
12: 110,602,943 (GRCm39) |
E2195K |
probably benign |
Het |
Fah |
T |
C |
7: 84,242,420 (GRCm39) |
D296G |
probably damaging |
Het |
Fam83g |
A |
G |
11: 61,593,504 (GRCm39) |
N346S |
probably damaging |
Het |
Fgl1 |
T |
A |
8: 41,644,638 (GRCm39) |
T289S |
possibly damaging |
Het |
Fmo1 |
A |
C |
1: 162,661,431 (GRCm39) |
L284R |
probably damaging |
Het |
Frem3 |
T |
A |
8: 81,395,430 (GRCm39) |
M1819K |
probably benign |
Het |
Fsip2 |
T |
A |
2: 82,818,762 (GRCm39) |
L4832M |
possibly damaging |
Het |
Fut1 |
T |
C |
7: 45,268,852 (GRCm39) |
W269R |
probably damaging |
Het |
Ggnbp2 |
A |
G |
11: 84,723,955 (GRCm39) |
Y638H |
probably damaging |
Het |
Gp2 |
T |
A |
7: 119,050,853 (GRCm39) |
I293F |
probably benign |
Het |
Gpi1 |
T |
C |
7: 33,929,580 (GRCm39) |
N20S |
probably benign |
Het |
Gxylt1 |
C |
T |
15: 93,152,273 (GRCm39) |
R222H |
probably damaging |
Het |
Hemgn |
T |
C |
4: 46,396,091 (GRCm39) |
K382E |
possibly damaging |
Het |
Hook3 |
T |
A |
8: 26,528,134 (GRCm39) |
E585D |
probably damaging |
Het |
Irf6 |
G |
A |
1: 192,851,613 (GRCm39) |
M401I |
probably benign |
Het |
Jmjd1c |
A |
G |
10: 67,085,529 (GRCm39) |
T2259A |
probably damaging |
Het |
Lactb |
T |
A |
9: 66,878,201 (GRCm39) |
R209S |
probably damaging |
Het |
Lonp2 |
A |
G |
8: 87,368,212 (GRCm39) |
D342G |
probably damaging |
Het |
Mmachc |
T |
C |
4: 116,563,194 (GRCm39) |
S54G |
probably damaging |
Het |
Mpp7 |
C |
A |
18: 7,350,977 (GRCm39) |
W573C |
probably damaging |
Het |
Or13e8 |
T |
A |
4: 43,697,011 (GRCm39) |
H54L |
possibly damaging |
Het |
Or5w1b |
T |
A |
2: 87,476,182 (GRCm39) |
Y95F |
probably benign |
Het |
Or6b2b |
A |
T |
1: 92,418,610 (GRCm39) |
I289N |
probably damaging |
Het |
Pappa2 |
A |
T |
1: 158,764,124 (GRCm39) |
D462E |
probably benign |
Het |
Pcdh12 |
A |
T |
18: 38,416,496 (GRCm39) |
F210I |
probably damaging |
Het |
Ppp1r12c |
A |
G |
7: 4,487,443 (GRCm39) |
|
probably null |
Het |
Prkce |
T |
A |
17: 86,803,446 (GRCm39) |
D448E |
possibly damaging |
Het |
Ptprb |
C |
A |
10: 116,175,584 (GRCm39) |
T1193K |
probably damaging |
Het |
Qrfpr |
T |
A |
3: 36,236,809 (GRCm39) |
E197D |
possibly damaging |
Het |
Rusc2 |
T |
A |
4: 43,416,568 (GRCm39) |
C625S |
probably benign |
Het |
Shcbp1 |
T |
G |
8: 4,791,968 (GRCm39) |
|
probably null |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Spag5 |
T |
A |
11: 78,196,143 (GRCm39) |
C449* |
probably null |
Het |
Stpg3 |
T |
C |
2: 25,103,862 (GRCm39) |
D158G |
probably damaging |
Het |
Tiprl |
C |
T |
1: 165,043,359 (GRCm39) |
E256K |
possibly damaging |
Het |
Tmem132c |
T |
A |
5: 127,640,631 (GRCm39) |
V934D |
probably damaging |
Het |
Topors |
A |
G |
4: 40,261,982 (GRCm39) |
V434A |
probably benign |
Het |
Usp11 |
A |
G |
X: 20,584,946 (GRCm39) |
Y731C |
probably damaging |
Het |
Vmn2r58 |
T |
A |
7: 41,513,387 (GRCm39) |
I419L |
probably benign |
Het |
Wfs1 |
C |
A |
5: 37,139,422 (GRCm39) |
R72L |
possibly damaging |
Het |
Zan |
T |
C |
5: 137,426,201 (GRCm39) |
D2525G |
unknown |
Het |
Zfp280c |
A |
G |
X: 47,652,715 (GRCm39) |
V285A |
probably benign |
Het |
Zfp511 |
T |
A |
7: 139,617,528 (GRCm39) |
F177I |
probably damaging |
Het |
Zfp964 |
A |
G |
8: 70,115,720 (GRCm39) |
M107V |
unknown |
Het |
Zmynd11 |
A |
G |
13: 9,760,256 (GRCm39) |
Y122H |
probably damaging |
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 |
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 |
R3418:Sycp2
|
UTSW |
2 |
178,043,446 (GRCm39) |
splice site |
probably benign |
|
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 |
|
|