Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700122O11Rik |
T |
C |
17: 48,348,273 (GRCm39) |
T55A |
probably benign |
Het |
3110070M22Rik |
T |
A |
13: 119,624,822 (GRCm39) |
|
probably benign |
Het |
Acot12 |
T |
A |
13: 91,918,221 (GRCm39) |
N171K |
probably benign |
Het |
Adam18 |
G |
A |
8: 25,104,859 (GRCm39) |
Q652* |
probably null |
Het |
Adgrv1 |
T |
C |
13: 81,705,277 (GRCm39) |
E791G |
probably damaging |
Het |
Aff1 |
C |
T |
5: 103,981,685 (GRCm39) |
S608L |
probably damaging |
Het |
Amfr |
A |
T |
8: 94,707,018 (GRCm39) |
F432L |
probably damaging |
Het |
Ankfn1 |
G |
A |
11: 89,332,284 (GRCm39) |
L421F |
possibly damaging |
Het |
Ankrd31 |
T |
C |
13: 97,014,733 (GRCm39) |
V1334A |
probably benign |
Het |
Ascc3 |
C |
T |
10: 50,608,858 (GRCm39) |
H1534Y |
possibly damaging |
Het |
Aste1 |
G |
A |
9: 105,273,880 (GRCm39) |
C40Y |
probably benign |
Het |
Atf3 |
T |
C |
1: 190,909,510 (GRCm39) |
H53R |
probably benign |
Het |
Bsn |
C |
A |
9: 107,990,800 (GRCm39) |
V1651F |
probably damaging |
Het |
Bsn |
A |
T |
9: 107,993,361 (GRCm39) |
L797Q |
probably damaging |
Het |
Bzw2 |
T |
C |
12: 36,180,131 (GRCm39) |
D32G |
probably damaging |
Het |
Cacna1e |
A |
T |
1: 154,361,458 (GRCm39) |
M531K |
possibly damaging |
Het |
Cep120 |
A |
G |
18: 53,851,592 (GRCm39) |
F567L |
possibly damaging |
Het |
Cit |
T |
C |
5: 116,084,914 (GRCm39) |
I815T |
probably benign |
Het |
Cnot6l |
G |
T |
5: 96,276,826 (GRCm39) |
Q121K |
probably benign |
Het |
Col4a2 |
G |
A |
8: 11,483,725 (GRCm39) |
G882R |
probably damaging |
Het |
Col6a3 |
A |
G |
1: 90,743,961 (GRCm39) |
F536L |
probably damaging |
Het |
Copg2 |
T |
A |
6: 30,793,721 (GRCm39) |
H394L |
possibly damaging |
Het |
Cst13 |
A |
G |
2: 148,670,165 (GRCm39) |
M112V |
possibly damaging |
Het |
Cyp2j7 |
G |
T |
4: 96,124,786 (GRCm39) |
N37K |
probably benign |
Het |
Cyp2u1 |
T |
A |
3: 131,091,449 (GRCm39) |
N357I |
possibly damaging |
Het |
Dars1 |
T |
C |
1: 128,344,945 (GRCm39) |
T4A |
probably benign |
Het |
Dclk1 |
G |
T |
3: 55,429,374 (GRCm39) |
C414F |
possibly damaging |
Het |
Dmbt1 |
A |
T |
7: 130,694,832 (GRCm39) |
Y1009F |
unknown |
Het |
Ebf4 |
T |
C |
2: 130,148,775 (GRCm39) |
Y117H |
probably damaging |
Het |
Eif2b4 |
A |
G |
5: 31,348,500 (GRCm39) |
Y196H |
probably benign |
Het |
Enpp2 |
C |
T |
15: 54,739,080 (GRCm39) |
R401H |
probably damaging |
Het |
Epo |
T |
C |
5: 137,484,017 (GRCm39) |
|
probably benign |
Het |
Gli1 |
T |
A |
10: 127,173,359 (GRCm39) |
T100S |
possibly damaging |
Het |
Gml2 |
T |
A |
15: 74,695,957 (GRCm39) |
F117Y |
probably benign |
Het |
Hivep1 |
T |
C |
13: 42,335,403 (GRCm39) |
V2314A |
probably benign |
Het |
Hspb8 |
A |
G |
5: 116,547,487 (GRCm39) |
I165T |
probably damaging |
Het |
Itgax |
A |
T |
7: 127,732,849 (GRCm39) |
T243S |
probably benign |
Het |
Itih4 |
G |
T |
14: 30,608,533 (GRCm39) |
L16F |
probably damaging |
Het |
Kmt5a |
C |
T |
5: 124,578,064 (GRCm39) |
|
probably benign |
Het |
Lamc1 |
T |
C |
1: 153,115,009 (GRCm39) |
E1089G |
probably benign |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Mcmbp |
A |
T |
7: 128,317,803 (GRCm39) |
N147K |
probably benign |
Het |
Mical2 |
C |
T |
7: 111,981,246 (GRCm39) |
L407F |
probably benign |
Het |
Mybpc2 |
A |
T |
7: 44,158,999 (GRCm39) |
V653D |
probably benign |
Het |
Myo3b |
G |
A |
2: 70,069,242 (GRCm39) |
V522I |
possibly damaging |
Het |
Nbr1 |
A |
G |
11: 101,456,590 (GRCm39) |
T156A |
possibly damaging |
Het |
Neb |
T |
A |
2: 52,039,291 (GRCm39) |
|
probably null |
Het |
Neb |
T |
A |
2: 52,116,546 (GRCm39) |
Y964F |
|
Het |
Nr2f2 |
T |
A |
7: 70,007,856 (GRCm39) |
I209F |
probably damaging |
Het |
Nwd2 |
A |
G |
5: 63,957,740 (GRCm39) |
T357A |
probably damaging |
Het |
Palld |
C |
T |
8: 61,969,691 (GRCm39) |
R1211H |
unknown |
Het |
Pcdhb19 |
T |
A |
18: 37,632,299 (GRCm39) |
V698E |
probably damaging |
Het |
Pcdhga6 |
C |
T |
18: 37,841,570 (GRCm39) |
P430L |
probably damaging |
Het |
Piezo2 |
A |
G |
18: 63,162,156 (GRCm39) |
L2225S |
possibly damaging |
Het |
Plekhf1 |
A |
T |
7: 37,921,203 (GRCm39) |
W122R |
probably damaging |
Het |
Pold3 |
A |
G |
7: 99,732,993 (GRCm39) |
S418P |
possibly damaging |
Het |
Poldip3 |
T |
C |
15: 83,019,589 (GRCm39) |
N180S |
probably benign |
Het |
Ppp1r21 |
C |
T |
17: 88,852,815 (GRCm39) |
R65* |
probably null |
Het |
Ppp1r3d |
A |
T |
2: 178,055,669 (GRCm39) |
V111E |
probably damaging |
Het |
Prrg4 |
T |
C |
2: 104,669,728 (GRCm39) |
I130V |
probably benign |
Het |
Psma5 |
A |
T |
3: 108,172,448 (GRCm39) |
T55S |
probably benign |
Het |
Rbm5 |
C |
A |
9: 107,627,252 (GRCm39) |
A440S |
probably benign |
Het |
Rdx |
A |
G |
9: 51,980,168 (GRCm39) |
K254E |
possibly damaging |
Het |
Rere |
A |
C |
4: 150,593,342 (GRCm39) |
Q312P |
unknown |
Het |
Rest |
T |
C |
5: 77,416,128 (GRCm39) |
V114A |
possibly damaging |
Het |
Rufy4 |
G |
T |
1: 74,171,879 (GRCm39) |
V201L |
probably benign |
Het |
Scyl1 |
T |
C |
19: 5,809,023 (GRCm39) |
E727G |
probably benign |
Het |
Serpinb6b |
T |
A |
13: 33,152,494 (GRCm39) |
M1K |
probably null |
Het |
Sgsm1 |
C |
A |
5: 113,436,741 (GRCm39) |
V30F |
probably damaging |
Het |
Skap1 |
A |
G |
11: 96,644,921 (GRCm39) |
D344G |
possibly damaging |
Het |
Slc26a7 |
T |
C |
4: 14,516,189 (GRCm39) |
T547A |
probably benign |
Het |
Slc6a3 |
C |
A |
13: 73,692,966 (GRCm39) |
S195R |
probably benign |
Het |
Sorbs1 |
T |
C |
19: 40,387,048 (GRCm39) |
D6G |
probably damaging |
Het |
Ssh2 |
A |
G |
11: 77,298,974 (GRCm39) |
Y107C |
possibly damaging |
Het |
Svil |
T |
C |
18: 5,057,294 (GRCm39) |
S581P |
probably benign |
Het |
Tbc1d14 |
T |
C |
5: 36,662,472 (GRCm39) |
T553A |
probably benign |
Het |
Tet3 |
T |
A |
6: 83,380,596 (GRCm39) |
Q524L |
possibly damaging |
Het |
Uckl1 |
A |
T |
2: 181,211,532 (GRCm39) |
V456E |
probably damaging |
Het |
Ucp2 |
T |
C |
7: 100,146,040 (GRCm39) |
F4S |
probably benign |
Het |
Vmn2r77 |
A |
G |
7: 86,444,442 (GRCm39) |
I32V |
probably benign |
Het |
Vmn2r89 |
T |
A |
14: 51,692,601 (GRCm39) |
Y135N |
probably benign |
Het |
Vtn |
A |
G |
11: 78,390,587 (GRCm39) |
E82G |
probably benign |
Het |
Zfp758 |
A |
G |
17: 22,593,925 (GRCm39) |
N137S |
probably benign |
Het |
Zgpat |
T |
A |
2: 181,021,646 (GRCm39) |
C357* |
probably null |
Het |
|
Other mutations in Spock3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01093:Spock3
|
APN |
8 |
63,801,993 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01716:Spock3
|
APN |
8 |
63,808,384 (GRCm39) |
missense |
unknown |
|
IGL02058:Spock3
|
APN |
8 |
63,698,232 (GRCm39) |
nonsense |
probably null |
|
IGL02450:Spock3
|
APN |
8 |
63,698,249 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02610:Spock3
|
APN |
8 |
63,798,771 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03046:Spock3
|
UTSW |
8 |
63,802,018 (GRCm39) |
critical splice donor site |
probably null |
|
R0044:Spock3
|
UTSW |
8 |
63,597,041 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0044:Spock3
|
UTSW |
8 |
63,597,041 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0084:Spock3
|
UTSW |
8 |
63,596,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R1422:Spock3
|
UTSW |
8 |
63,597,023 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1469:Spock3
|
UTSW |
8 |
63,404,934 (GRCm39) |
missense |
probably damaging |
0.99 |
R1469:Spock3
|
UTSW |
8 |
63,404,934 (GRCm39) |
missense |
probably damaging |
0.99 |
R1484:Spock3
|
UTSW |
8 |
63,673,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Spock3
|
UTSW |
8 |
63,802,011 (GRCm39) |
missense |
probably damaging |
0.99 |
R1729:Spock3
|
UTSW |
8 |
63,802,011 (GRCm39) |
missense |
probably damaging |
0.99 |
R1739:Spock3
|
UTSW |
8 |
63,801,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R2057:Spock3
|
UTSW |
8 |
63,698,204 (GRCm39) |
nonsense |
probably null |
|
R2340:Spock3
|
UTSW |
8 |
63,798,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Spock3
|
UTSW |
8 |
63,798,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Spock3
|
UTSW |
8 |
63,798,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R3733:Spock3
|
UTSW |
8 |
63,798,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R3763:Spock3
|
UTSW |
8 |
63,597,049 (GRCm39) |
critical splice donor site |
probably null |
|
R5000:Spock3
|
UTSW |
8 |
63,698,158 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5069:Spock3
|
UTSW |
8 |
63,808,299 (GRCm39) |
missense |
probably benign |
0.01 |
R5076:Spock3
|
UTSW |
8 |
63,798,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R5232:Spock3
|
UTSW |
8 |
63,798,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R5329:Spock3
|
UTSW |
8 |
63,798,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R5621:Spock3
|
UTSW |
8 |
63,597,040 (GRCm39) |
missense |
probably benign |
0.19 |
R5882:Spock3
|
UTSW |
8 |
63,596,965 (GRCm39) |
missense |
probably benign |
0.03 |
R5888:Spock3
|
UTSW |
8 |
63,808,334 (GRCm39) |
missense |
unknown |
|
R5902:Spock3
|
UTSW |
8 |
63,808,336 (GRCm39) |
missense |
unknown |
|
R6991:Spock3
|
UTSW |
8 |
63,808,415 (GRCm39) |
makesense |
probably null |
|
R7317:Spock3
|
UTSW |
8 |
63,566,590 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7970:Spock3
|
UTSW |
8 |
63,798,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R8030:Spock3
|
UTSW |
8 |
63,805,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R8392:Spock3
|
UTSW |
8 |
63,808,345 (GRCm39) |
missense |
unknown |
|
R8889:Spock3
|
UTSW |
8 |
63,404,986 (GRCm39) |
nonsense |
probably null |
|
R8892:Spock3
|
UTSW |
8 |
63,404,986 (GRCm39) |
nonsense |
probably null |
|
R9065:Spock3
|
UTSW |
8 |
63,801,989 (GRCm39) |
missense |
probably damaging |
0.98 |
R9199:Spock3
|
UTSW |
8 |
63,798,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|