Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
T |
A |
5: 144,982,181 (GRCm39) |
Y255* |
probably null |
Het |
1810024B03Rik |
A |
G |
2: 127,029,196 (GRCm39) |
M1T |
probably null |
Het |
4930503L19Rik |
T |
C |
18: 70,600,451 (GRCm39) |
D386G |
probably damaging |
Het |
Ace2 |
T |
A |
X: 162,958,947 (GRCm39) |
N601K |
probably benign |
Het |
Adam4 |
A |
C |
12: 81,468,198 (GRCm39) |
I141R |
probably damaging |
Het |
Adcy10 |
G |
A |
1: 165,340,699 (GRCm39) |
G235S |
probably benign |
Het |
Adcy5 |
G |
A |
16: 35,114,387 (GRCm39) |
V997I |
probably benign |
Het |
Aff2 |
T |
G |
X: 68,907,680 (GRCm39) |
W1221G |
possibly damaging |
Het |
Ankrd44 |
T |
C |
1: 54,802,917 (GRCm39) |
N194D |
probably benign |
Het |
Apba2 |
T |
G |
7: 64,395,528 (GRCm39) |
L668R |
probably damaging |
Het |
Asph |
T |
C |
4: 9,604,581 (GRCm39) |
D152G |
probably damaging |
Het |
Bcl3 |
C |
G |
7: 19,553,991 (GRCm39) |
V126L |
probably benign |
Het |
Cd163 |
A |
G |
6: 124,289,619 (GRCm39) |
T446A |
probably benign |
Het |
Cd209g |
C |
T |
8: 4,184,995 (GRCm39) |
|
probably benign |
Het |
Cdadc1 |
A |
T |
14: 59,823,901 (GRCm39) |
V197E |
probably damaging |
Het |
CN725425 |
T |
C |
15: 91,144,966 (GRCm39) |
C610R |
possibly damaging |
Het |
Col6a2 |
A |
G |
10: 76,446,995 (GRCm39) |
|
probably null |
Het |
Coro7 |
A |
G |
16: 4,450,121 (GRCm39) |
L576P |
possibly damaging |
Het |
Dgkb |
T |
A |
12: 38,266,030 (GRCm39) |
V503E |
probably benign |
Het |
Dhx57 |
A |
T |
17: 80,567,665 (GRCm39) |
L806* |
probably null |
Het |
Dlec1 |
T |
C |
9: 118,944,070 (GRCm39) |
V373A |
probably benign |
Het |
Dnah11 |
G |
T |
12: 117,894,913 (GRCm39) |
R3645S |
probably benign |
Het |
Dnhd1 |
T |
C |
7: 105,343,602 (GRCm39) |
S1649P |
probably benign |
Het |
Draxin |
T |
G |
4: 148,192,420 (GRCm39) |
K297N |
probably damaging |
Het |
Epha7 |
T |
C |
4: 28,951,401 (GRCm39) |
S841P |
probably damaging |
Het |
Esp8 |
T |
G |
17: 40,841,166 (GRCm39) |
D142E |
unknown |
Het |
F5 |
T |
G |
1: 164,007,018 (GRCm39) |
V274G |
probably damaging |
Het |
Fancc |
T |
C |
13: 63,465,283 (GRCm39) |
S475G |
probably benign |
Het |
Fmo3 |
T |
C |
1: 162,781,901 (GRCm39) |
N484S |
probably benign |
Het |
Focad |
T |
C |
4: 88,267,126 (GRCm39) |
Y1046H |
unknown |
Het |
Furin |
C |
T |
7: 80,041,032 (GRCm39) |
G602D |
probably damaging |
Het |
Fut8 |
A |
T |
12: 77,411,744 (GRCm39) |
I69L |
probably benign |
Het |
Gnai3 |
A |
G |
3: 108,030,928 (GRCm39) |
I78T |
probably benign |
Het |
Gpr182 |
T |
C |
10: 127,586,940 (GRCm39) |
I4V |
probably benign |
Het |
Gpr63 |
T |
C |
4: 25,007,447 (GRCm39) |
M57T |
probably benign |
Het |
Grm1 |
T |
A |
10: 10,595,667 (GRCm39) |
T654S |
probably benign |
Het |
Gtf2h4 |
T |
C |
17: 35,979,531 (GRCm39) |
T371A |
probably benign |
Het |
Helq |
T |
C |
5: 100,938,066 (GRCm39) |
N460S |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,594,868 (GRCm39) |
N1867S |
probably benign |
Het |
Hsh2d |
G |
A |
8: 72,954,304 (GRCm39) |
D229N |
probably benign |
Het |
Iigp1c |
G |
A |
18: 60,378,489 (GRCm39) |
R8H |
probably benign |
Het |
Inpp5j |
A |
G |
11: 3,449,644 (GRCm39) |
Y713H |
probably damaging |
Het |
Ints6 |
A |
T |
14: 62,942,200 (GRCm39) |
V511D |
possibly damaging |
Het |
Irag2 |
G |
A |
6: 145,111,013 (GRCm39) |
A237T |
probably benign |
Het |
Itga4 |
A |
G |
2: 79,109,461 (GRCm39) |
Y220C |
probably damaging |
Het |
Itgav |
T |
G |
2: 83,624,614 (GRCm39) |
S735A |
possibly damaging |
Het |
Kctd16 |
A |
G |
18: 40,391,492 (GRCm39) |
I27V |
probably benign |
Het |
Klhl6 |
T |
C |
16: 19,772,343 (GRCm39) |
E334G |
probably damaging |
Het |
Ltbp1 |
T |
A |
17: 75,532,274 (GRCm39) |
L116H |
probably damaging |
Het |
Magohb |
T |
A |
6: 131,262,660 (GRCm39) |
H98L |
probably benign |
Het |
Mgat2 |
A |
G |
12: 69,232,166 (GRCm39) |
T247A |
probably benign |
Het |
Mtif2 |
G |
A |
11: 29,483,398 (GRCm39) |
|
probably null |
Het |
Myrfl |
T |
C |
10: 116,664,878 (GRCm39) |
E384G |
probably damaging |
Het |
Nfam1 |
G |
T |
15: 82,917,410 (GRCm39) |
R8S |
probably benign |
Het |
Numa1 |
T |
C |
7: 101,644,731 (GRCm39) |
S236P |
possibly damaging |
Het |
Or14c46 |
A |
T |
7: 85,918,865 (GRCm39) |
I44N |
probably damaging |
Het |
Or2w3b |
T |
C |
11: 58,623,865 (GRCm39) |
N42S |
probably damaging |
Het |
Or5m10b |
T |
C |
2: 85,699,863 (GRCm39) |
F309S |
probably benign |
Het |
Or6c207 |
T |
C |
10: 129,104,368 (GRCm39) |
T275A |
probably benign |
Het |
Orc4 |
C |
T |
2: 48,795,433 (GRCm39) |
S431N |
probably benign |
Het |
Pax2 |
T |
C |
19: 44,750,300 (GRCm39) |
V129A |
probably damaging |
Het |
Pcdhb15 |
A |
G |
18: 37,607,572 (GRCm39) |
D268G |
probably damaging |
Het |
Pdcd1 |
G |
A |
1: 93,967,107 (GRCm39) |
R264C |
probably damaging |
Het |
Pi15 |
T |
A |
1: 17,691,872 (GRCm39) |
M187K |
probably benign |
Het |
Plag1 |
C |
T |
4: 3,904,546 (GRCm39) |
C215Y |
probably damaging |
Het |
Plagl1 |
A |
G |
10: 13,002,926 (GRCm39) |
T65A |
probably benign |
Het |
Pramel51 |
T |
C |
12: 88,144,328 (GRCm39) |
T162A |
probably benign |
Het |
Prss48 |
T |
A |
3: 85,908,228 (GRCm39) |
Q18L |
probably benign |
Het |
Prune2 |
T |
A |
19: 17,102,582 (GRCm39) |
C2580* |
probably null |
Het |
Rab40b |
T |
A |
11: 121,250,432 (GRCm39) |
Q74L |
probably damaging |
Het |
Raf1 |
A |
G |
6: 115,600,491 (GRCm39) |
I376T |
probably benign |
Het |
Rbm46 |
A |
T |
3: 82,772,575 (GRCm39) |
F186I |
probably damaging |
Het |
Reps1 |
C |
T |
10: 17,998,867 (GRCm39) |
T720M |
possibly damaging |
Het |
Rgs22 |
A |
G |
15: 36,054,855 (GRCm39) |
M649T |
probably benign |
Het |
Rhot1 |
C |
T |
11: 80,134,264 (GRCm39) |
R47* |
probably null |
Het |
Rhox2f |
A |
G |
X: 36,753,124 (GRCm39) |
Y8C |
possibly damaging |
Het |
Rnf17 |
A |
G |
14: 56,760,007 (GRCm39) |
Y1604C |
probably damaging |
Het |
Rnf40 |
T |
C |
7: 127,201,756 (GRCm39) |
C943R |
probably damaging |
Het |
Ropn1l |
A |
T |
15: 31,451,295 (GRCm39) |
M63K |
probably benign |
Het |
Sbf2 |
C |
A |
7: 110,027,494 (GRCm39) |
V501F |
probably damaging |
Het |
Sh3bp1 |
T |
A |
15: 78,791,467 (GRCm39) |
M354K |
probably damaging |
Het |
Sipa1l3 |
T |
C |
7: 29,087,455 (GRCm39) |
H590R |
possibly damaging |
Het |
Slco6d1 |
T |
A |
1: 98,394,422 (GRCm39) |
C369S |
probably benign |
Het |
Sulf1 |
T |
C |
1: 12,875,418 (GRCm39) |
Y143H |
probably damaging |
Het |
Tiam2 |
A |
T |
17: 3,488,956 (GRCm39) |
R755* |
probably null |
Het |
Trim12c |
C |
A |
7: 103,994,169 (GRCm39) |
L228F |
probably damaging |
Het |
Ttc23l |
G |
T |
15: 10,530,743 (GRCm39) |
Q290K |
probably benign |
Het |
Uba3 |
T |
C |
6: 97,168,221 (GRCm39) |
|
probably null |
Het |
Ugt1a10 |
A |
G |
1: 87,983,817 (GRCm39) |
E205G |
probably damaging |
Het |
Ugt3a1 |
T |
A |
15: 9,351,206 (GRCm39) |
S72T |
probably benign |
Het |
Upk3bl |
C |
T |
5: 136,088,648 (GRCm39) |
T113I |
probably damaging |
Het |
Uspl1 |
T |
A |
5: 149,124,644 (GRCm39) |
D20E |
probably damaging |
Het |
Vmn2r19 |
G |
A |
6: 123,313,102 (GRCm39) |
G724E |
probably damaging |
Het |
Vmn2r63 |
T |
A |
7: 42,583,129 (GRCm39) |
K29* |
probably null |
Het |
Vwf |
C |
T |
6: 125,619,744 (GRCm39) |
A1474V |
probably benign |
Het |
Xpc |
C |
T |
6: 91,468,208 (GRCm39) |
A860T |
probably benign |
Het |
Zfp462 |
A |
G |
4: 55,013,689 (GRCm39) |
H737R |
probably damaging |
Het |
Zfp536 |
T |
C |
7: 37,180,244 (GRCm39) |
D787G |
probably damaging |
Het |
Zfp692 |
A |
G |
11: 58,205,053 (GRCm39) |
H434R |
probably damaging |
Het |
|
Other mutations in Zp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Zp1
|
APN |
19 |
10,896,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01504:Zp1
|
APN |
19 |
10,896,375 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02260:Zp1
|
APN |
19 |
10,894,078 (GRCm39) |
unclassified |
probably benign |
|
IGL02465:Zp1
|
APN |
19 |
10,897,851 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02634:Zp1
|
APN |
19 |
10,896,871 (GRCm39) |
unclassified |
probably benign |
|
IGL02714:Zp1
|
APN |
19 |
10,895,976 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03234:Zp1
|
APN |
19 |
10,892,187 (GRCm39) |
splice site |
probably benign |
|
IGL03404:Zp1
|
APN |
19 |
10,891,825 (GRCm39) |
unclassified |
probably benign |
|
R0504:Zp1
|
UTSW |
19 |
10,893,571 (GRCm39) |
missense |
probably damaging |
0.98 |
R1028:Zp1
|
UTSW |
19 |
10,896,275 (GRCm39) |
missense |
probably benign |
0.01 |
R1279:Zp1
|
UTSW |
19 |
10,895,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R1460:Zp1
|
UTSW |
19 |
10,896,242 (GRCm39) |
missense |
probably benign |
|
R3425:Zp1
|
UTSW |
19 |
10,895,956 (GRCm39) |
missense |
probably benign |
0.00 |
R3832:Zp1
|
UTSW |
19 |
10,893,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R4420:Zp1
|
UTSW |
19 |
10,892,124 (GRCm39) |
splice site |
probably null |
|
R4669:Zp1
|
UTSW |
19 |
10,896,269 (GRCm39) |
missense |
probably benign |
0.31 |
R4849:Zp1
|
UTSW |
19 |
10,896,198 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5134:Zp1
|
UTSW |
19 |
10,897,926 (GRCm39) |
missense |
probably benign |
0.29 |
R5170:Zp1
|
UTSW |
19 |
10,897,918 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5510:Zp1
|
UTSW |
19 |
10,896,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R6284:Zp1
|
UTSW |
19 |
10,893,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R6307:Zp1
|
UTSW |
19 |
10,894,084 (GRCm39) |
missense |
probably null |
0.45 |
R6378:Zp1
|
UTSW |
19 |
10,892,217 (GRCm39) |
missense |
probably benign |
0.15 |
R6608:Zp1
|
UTSW |
19 |
10,896,344 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6697:Zp1
|
UTSW |
19 |
10,892,199 (GRCm39) |
missense |
probably benign |
0.05 |
R6862:Zp1
|
UTSW |
19 |
10,893,877 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7054:Zp1
|
UTSW |
19 |
10,896,104 (GRCm39) |
missense |
probably damaging |
0.98 |
R7253:Zp1
|
UTSW |
19 |
10,893,933 (GRCm39) |
missense |
probably damaging |
0.99 |
R7483:Zp1
|
UTSW |
19 |
10,895,280 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7591:Zp1
|
UTSW |
19 |
10,896,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R8857:Zp1
|
UTSW |
19 |
10,893,888 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Zp1
|
UTSW |
19 |
10,895,278 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Zp1
|
UTSW |
19 |
10,895,968 (GRCm39) |
missense |
probably damaging |
1.00 |
|