Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
A |
G |
3: 121,964,592 (GRCm39) |
E925G |
probably damaging |
Het |
Abca9 |
T |
G |
11: 110,006,280 (GRCm39) |
Q1275P |
probably benign |
Het |
Adgrl1 |
T |
A |
8: 84,657,870 (GRCm39) |
M492K |
probably benign |
Het |
Ankrd50 |
T |
A |
3: 38,537,234 (GRCm39) |
K3* |
probably null |
Het |
Arl5b |
T |
C |
2: 15,079,848 (GRCm39) |
S140P |
probably damaging |
Het |
Armc1 |
T |
C |
3: 19,211,840 (GRCm39) |
|
probably benign |
Het |
Ascc1 |
T |
C |
10: 59,840,663 (GRCm39) |
I8T |
probably benign |
Het |
Bche |
A |
G |
3: 73,608,805 (GRCm39) |
V207A |
probably damaging |
Het |
Cacna2d3 |
A |
G |
14: 28,627,259 (GRCm39) |
L1080P |
probably benign |
Het |
Ceacam3 |
C |
A |
7: 16,895,779 (GRCm39) |
A583D |
probably damaging |
Het |
Cep290 |
C |
T |
10: 100,373,299 (GRCm39) |
A1193V |
probably benign |
Het |
Clcn1 |
T |
C |
6: 42,290,046 (GRCm39) |
I827T |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Col28a1 |
T |
C |
6: 8,175,641 (GRCm39) |
D69G |
possibly damaging |
Het |
Cts3 |
A |
G |
13: 61,712,806 (GRCm39) |
W305R |
probably damaging |
Het |
Dmwd |
T |
C |
7: 18,815,084 (GRCm39) |
I578T |
possibly damaging |
Het |
Dnmt3a |
G |
A |
12: 3,949,883 (GRCm39) |
V559M |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,016,549 (GRCm39) |
V70A |
possibly damaging |
Het |
Eml6 |
A |
G |
11: 29,752,434 (GRCm39) |
V993A |
probably benign |
Het |
Etl4 |
T |
A |
2: 20,812,117 (GRCm39) |
L1768* |
probably null |
Het |
F11 |
A |
G |
8: 45,701,675 (GRCm39) |
S353P |
probably damaging |
Het |
Fat3 |
T |
G |
9: 15,881,167 (GRCm39) |
D3235A |
probably damaging |
Het |
Fbxo36 |
T |
A |
1: 84,877,823 (GRCm39) |
F162I |
probably damaging |
Het |
Fgfrl1 |
T |
C |
5: 108,852,897 (GRCm39) |
W200R |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,811,064 (GRCm39) |
M2461T |
possibly damaging |
Het |
Fut1 |
A |
G |
7: 45,268,643 (GRCm39) |
Y144C |
probably benign |
Het |
Gprin3 |
G |
A |
6: 59,331,134 (GRCm39) |
A391V |
probably benign |
Het |
H2-Q4 |
A |
G |
17: 35,598,973 (GRCm39) |
E81G |
probably damaging |
Het |
Hacd3 |
A |
G |
9: 64,908,311 (GRCm39) |
S162P |
probably damaging |
Het |
Itga1 |
A |
T |
13: 115,114,150 (GRCm39) |
H918Q |
probably benign |
Het |
Lrp5 |
C |
A |
19: 3,647,430 (GRCm39) |
D1271Y |
probably damaging |
Het |
Lsm8 |
C |
T |
6: 18,849,643 (GRCm39) |
T17I |
probably benign |
Het |
Mup4 |
T |
A |
4: 59,958,145 (GRCm39) |
D141V |
probably damaging |
Het |
Nckap5 |
G |
A |
1: 125,955,146 (GRCm39) |
H405Y |
probably benign |
Het |
Obscn |
T |
C |
11: 59,022,472 (GRCm39) |
R758G |
possibly damaging |
Het |
Or12k8 |
T |
C |
2: 36,974,986 (GRCm39) |
Y258C |
probably benign |
Het |
Ostf1 |
T |
C |
19: 18,562,026 (GRCm39) |
K190R |
probably benign |
Het |
Pnldc1 |
A |
T |
17: 13,118,777 (GRCm39) |
V197E |
probably damaging |
Het |
Ptprc |
A |
G |
1: 138,016,270 (GRCm39) |
S531P |
probably damaging |
Het |
Ryr3 |
C |
T |
2: 112,516,973 (GRCm39) |
E3318K |
probably damaging |
Het |
Scamp2 |
T |
C |
9: 57,484,995 (GRCm39) |
V67A |
possibly damaging |
Het |
Serpina3g |
C |
A |
12: 104,207,421 (GRCm39) |
L195M |
probably damaging |
Het |
Siglec1 |
G |
T |
2: 130,916,395 (GRCm39) |
T1185N |
possibly damaging |
Het |
Tmprss15 |
T |
G |
16: 78,854,578 (GRCm39) |
T277P |
probably damaging |
Het |
Trim34b |
C |
T |
7: 103,978,876 (GRCm39) |
S41L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,557,705 (GRCm39) |
T21507A |
possibly damaging |
Het |
Umad1 |
T |
C |
6: 8,427,161 (GRCm39) |
V138A |
possibly damaging |
Het |
Zfp523 |
A |
G |
17: 28,414,183 (GRCm39) |
I72M |
probably damaging |
Het |
Zfp655 |
C |
T |
5: 145,181,356 (GRCm39) |
R405C |
probably benign |
Het |
Zfp715 |
G |
A |
7: 42,948,692 (GRCm39) |
R423C |
possibly 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 |
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 |
|
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 |
|
|