Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
A |
C |
1: 130,671,130 (GRCm39) |
T451P |
probably benign |
Het |
Actbl2 |
A |
G |
13: 111,392,310 (GRCm39) |
E215G |
probably damaging |
Het |
Adh6b |
A |
G |
3: 138,058,545 (GRCm39) |
T198A |
possibly damaging |
Het |
Bicd2 |
A |
G |
13: 49,531,804 (GRCm39) |
K349E |
probably damaging |
Het |
Bsnd |
T |
A |
4: 106,349,231 (GRCm39) |
D3V |
probably damaging |
Het |
Cd83 |
T |
A |
13: 43,953,147 (GRCm39) |
L142Q |
probably null |
Het |
Cdh20 |
A |
G |
1: 110,065,655 (GRCm39) |
E643G |
probably damaging |
Het |
Ces1b |
T |
G |
8: 93,783,594 (GRCm39) |
E542A |
possibly damaging |
Het |
Cfhr2 |
A |
G |
1: 139,738,762 (GRCm39) |
|
probably benign |
Het |
Clip1 |
T |
C |
5: 123,769,186 (GRCm39) |
D471G |
probably damaging |
Het |
Cntn5 |
C |
A |
9: 10,048,683 (GRCm39) |
|
probably null |
Het |
Cntnap2 |
A |
T |
6: 46,147,179 (GRCm39) |
D475V |
probably damaging |
Het |
Cntnap5c |
T |
C |
17: 58,612,679 (GRCm39) |
F906S |
probably benign |
Het |
Cobll1 |
A |
T |
2: 64,928,663 (GRCm39) |
S888T |
probably damaging |
Het |
Csf2rb |
G |
A |
15: 78,223,103 (GRCm39) |
R105Q |
probably benign |
Het |
Ctnnd1 |
C |
A |
2: 84,454,806 (GRCm39) |
M1I |
probably null |
Het |
Cxxc1 |
C |
T |
18: 74,352,481 (GRCm39) |
Q354* |
probably null |
Het |
Dnhd1 |
A |
G |
7: 105,304,930 (GRCm39) |
D324G |
possibly damaging |
Het |
Donson |
T |
C |
16: 91,478,196 (GRCm39) |
D435G |
possibly damaging |
Het |
Ephb1 |
T |
C |
9: 101,887,218 (GRCm39) |
K474E |
possibly damaging |
Het |
Erbin |
A |
G |
13: 104,004,638 (GRCm39) |
L130P |
probably damaging |
Het |
Fam221a |
C |
T |
6: 49,355,411 (GRCm39) |
T171I |
probably damaging |
Het |
Farp2 |
A |
G |
1: 93,456,332 (GRCm39) |
E5G |
probably damaging |
Het |
Fblim1 |
A |
G |
4: 141,317,431 (GRCm39) |
S85P |
possibly damaging |
Het |
Fhl2 |
A |
T |
1: 43,162,761 (GRCm39) |
C251* |
probably null |
Het |
Glis2 |
T |
C |
16: 4,429,735 (GRCm39) |
|
probably null |
Het |
Gm10715 |
A |
C |
9: 3,038,062 (GRCm39) |
|
probably benign |
Het |
Gm10717 |
C |
T |
9: 3,031,999 (GRCm39) |
P127S |
probably benign |
Het |
Heatr6 |
T |
C |
11: 83,651,762 (GRCm39) |
L246P |
probably damaging |
Het |
Igkv5-39 |
G |
A |
6: 69,877,457 (GRCm39) |
P100S |
probably benign |
Het |
Jup |
T |
C |
11: 100,269,204 (GRCm39) |
D403G |
probably benign |
Het |
Kank1 |
T |
C |
19: 25,388,963 (GRCm39) |
Y879H |
probably damaging |
Het |
Kcna3 |
G |
A |
3: 106,944,369 (GRCm39) |
E211K |
probably damaging |
Het |
Klc3 |
A |
T |
7: 19,129,049 (GRCm39) |
I440N |
possibly damaging |
Het |
Mmp1b |
T |
C |
9: 7,384,709 (GRCm39) |
T280A |
probably benign |
Het |
Nat3 |
A |
T |
8: 68,000,160 (GRCm39) |
Q13L |
probably benign |
Het |
Nckap1l |
A |
G |
15: 103,372,963 (GRCm39) |
N272S |
probably benign |
Het |
Nrn1 |
C |
A |
13: 36,914,080 (GRCm39) |
|
probably null |
Het |
Nsd3 |
T |
C |
8: 26,130,922 (GRCm39) |
S96P |
probably damaging |
Het |
Ntaq1 |
A |
G |
15: 58,011,833 (GRCm39) |
S65G |
probably benign |
Het |
Nudt16l1 |
C |
T |
16: 4,757,131 (GRCm39) |
R43C |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,891,310 (GRCm39) |
Q7074L |
unknown |
Het |
Or4p20 |
A |
G |
2: 88,253,832 (GRCm39) |
V179A |
probably benign |
Het |
Or5m12 |
A |
G |
2: 85,734,733 (GRCm39) |
S222P |
probably damaging |
Het |
Or5p78 |
A |
T |
7: 108,211,669 (GRCm39) |
I52F |
probably damaging |
Het |
Or6c206 |
T |
A |
10: 129,097,136 (GRCm39) |
|
probably null |
Het |
Or8b37 |
T |
G |
9: 37,959,345 (GRCm39) |
Y276D |
probably damaging |
Het |
Or8k30 |
T |
A |
2: 86,339,290 (GRCm39) |
N162K |
probably benign |
Het |
P4htm |
C |
T |
9: 108,460,055 (GRCm39) |
D240N |
probably benign |
Het |
Plekhm2 |
A |
T |
4: 141,369,835 (GRCm39) |
|
probably benign |
Het |
Plppr5 |
T |
C |
3: 117,456,228 (GRCm39) |
S250P |
probably damaging |
Het |
Pmis2 |
T |
C |
7: 30,370,919 (GRCm39) |
K12E |
probably benign |
Het |
Ppox |
A |
T |
1: 171,105,066 (GRCm39) |
L374* |
probably null |
Het |
Rcc1 |
C |
T |
4: 132,065,067 (GRCm39) |
R139H |
probably benign |
Het |
Tdo2 |
A |
G |
3: 81,883,004 (GRCm39) |
|
probably benign |
Het |
Tent2 |
A |
T |
13: 93,285,449 (GRCm39) |
N436K |
probably damaging |
Het |
Thbs2 |
A |
G |
17: 14,904,389 (GRCm39) |
I326T |
probably benign |
Het |
Thrap3 |
T |
C |
4: 126,059,157 (GRCm39) |
|
probably benign |
Het |
Ttc6 |
A |
T |
12: 57,622,654 (GRCm39) |
M18L |
probably benign |
Het |
Ttn |
C |
T |
2: 76,604,924 (GRCm39) |
V18337I |
probably damaging |
Het |
Txndc2 |
A |
G |
17: 65,946,601 (GRCm39) |
S34P |
possibly damaging |
Het |
Vps72 |
T |
A |
3: 95,026,545 (GRCm39) |
C163* |
probably null |
Het |
Zfp831 |
T |
A |
2: 174,486,945 (GRCm39) |
I540N |
possibly damaging |
Het |
|
Other mutations in Speer4c1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02796:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02799:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02837:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02984:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02988:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02991:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03014:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03046:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03047:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03050:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03055:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03097:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03098:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03134:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03138:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03147:Speer4c1
|
UTSW |
5 |
15,919,214 (GRCm39) |
utr 5 prime |
probably benign |
|
R2122:Speer4c1
|
UTSW |
5 |
15,919,115 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7176:Speer4c1
|
UTSW |
5 |
15,916,536 (GRCm39) |
missense |
probably benign |
0.00 |
R7849:Speer4c1
|
UTSW |
5 |
15,915,925 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8996:Speer4c1
|
UTSW |
5 |
15,915,886 (GRCm39) |
missense |
probably benign |
0.35 |
R9747:Speer4c1
|
UTSW |
5 |
15,916,652 (GRCm39) |
missense |
probably benign |
0.01 |
|