Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
T |
C |
7: 40,643,111 (GRCm39) |
L260S |
probably benign |
Het |
9130230L23Rik |
A |
T |
5: 66,145,771 (GRCm39) |
S113R |
unknown |
Het |
Abcc5 |
G |
A |
16: 20,211,293 (GRCm39) |
P557S |
probably benign |
Het |
Acad11 |
A |
G |
9: 103,958,466 (GRCm39) |
T245A |
probably damaging |
Het |
Acap2 |
A |
G |
16: 30,946,155 (GRCm39) |
F263L |
probably damaging |
Het |
Ankle2 |
A |
T |
5: 110,385,632 (GRCm39) |
N327I |
probably benign |
Het |
Appl1 |
T |
C |
14: 26,685,617 (GRCm39) |
E67G |
probably benign |
Het |
Arfgef3 |
A |
T |
10: 18,506,211 (GRCm39) |
C864S |
possibly damaging |
Het |
Arhgap20 |
A |
G |
9: 51,751,802 (GRCm39) |
I418V |
probably benign |
Het |
Arhgef2 |
A |
T |
3: 88,539,610 (GRCm39) |
N102Y |
probably damaging |
Het |
Car9 |
G |
T |
4: 43,513,089 (GRCm39) |
E431D |
probably damaging |
Het |
Cbfa2t2 |
T |
C |
2: 154,342,374 (GRCm39) |
I30T |
probably benign |
Het |
Cd40 |
A |
T |
2: 164,904,255 (GRCm39) |
D34V |
possibly damaging |
Het |
Chrnb2 |
T |
A |
3: 89,670,674 (GRCm39) |
|
probably null |
Het |
Chsy1 |
T |
G |
7: 65,759,977 (GRCm39) |
|
probably null |
Het |
Cpne6 |
A |
G |
14: 55,751,751 (GRCm39) |
T245A |
possibly damaging |
Het |
Cpsf1 |
T |
A |
15: 76,481,475 (GRCm39) |
K1159* |
probably null |
Het |
Crisp1 |
T |
A |
17: 40,618,668 (GRCm39) |
E64D |
possibly damaging |
Het |
D3Ertd751e |
A |
G |
3: 41,756,986 (GRCm39) |
|
probably null |
Het |
Dennd11 |
A |
G |
6: 40,386,098 (GRCm39) |
V333A |
possibly damaging |
Het |
Dnah7b |
T |
A |
1: 46,234,532 (GRCm39) |
L1488Q |
probably damaging |
Het |
Dnm2 |
G |
A |
9: 21,416,863 (GRCm39) |
G799R |
possibly damaging |
Het |
Elp2 |
G |
A |
18: 24,739,956 (GRCm39) |
V61I |
probably damaging |
Het |
Epb41l3 |
T |
C |
17: 69,573,135 (GRCm39) |
L388P |
|
Het |
Fry |
A |
T |
5: 150,360,458 (GRCm39) |
S2035C |
probably damaging |
Het |
Gas8 |
T |
C |
8: 124,257,707 (GRCm39) |
F385L |
probably benign |
Het |
Gstp2 |
T |
A |
19: 4,091,065 (GRCm39) |
R85W |
probably benign |
Het |
Ighv1-20 |
T |
A |
12: 114,687,810 (GRCm39) |
I6F |
possibly damaging |
Het |
Inpp4b |
T |
A |
8: 82,798,374 (GRCm39) |
M854K |
probably damaging |
Het |
Kif15 |
A |
G |
9: 122,817,014 (GRCm39) |
E538G |
probably damaging |
Het |
Large2 |
T |
C |
2: 92,196,373 (GRCm39) |
T485A |
probably benign |
Het |
Lmo3 |
T |
A |
6: 138,398,363 (GRCm39) |
|
probably benign |
Het |
Lyg1 |
G |
A |
1: 37,988,936 (GRCm39) |
P95S |
probably benign |
Het |
Lyst |
A |
G |
13: 13,932,028 (GRCm39) |
H3552R |
probably benign |
Het |
Mtif2 |
C |
T |
11: 29,490,115 (GRCm39) |
S385L |
probably benign |
Het |
Muc4 |
A |
T |
16: 32,575,710 (GRCm39) |
I1737F |
unknown |
Het |
Mug1 |
T |
C |
6: 121,847,611 (GRCm39) |
|
probably null |
Het |
Mx1 |
G |
T |
16: 97,253,286 (GRCm39) |
Q350K |
probably benign |
Het |
Mylk3 |
G |
T |
8: 86,085,726 (GRCm39) |
D269E |
probably benign |
Het |
Myo3a |
A |
T |
2: 22,448,332 (GRCm39) |
K974* |
probably null |
Het |
Nectin4 |
G |
T |
1: 171,208,031 (GRCm39) |
R141L |
probably benign |
Het |
Nlgn2 |
T |
C |
11: 69,716,795 (GRCm39) |
H582R |
probably damaging |
Het |
Or51ab3 |
T |
A |
7: 103,201,298 (GRCm39) |
M102K |
probably damaging |
Het |
Or51e1 |
T |
A |
7: 102,359,226 (GRCm39) |
Y253* |
probably null |
Het |
Pi16 |
C |
A |
17: 29,538,208 (GRCm39) |
P7Q |
possibly damaging |
Het |
Psmd11 |
C |
A |
11: 80,347,128 (GRCm39) |
L171I |
probably benign |
Het |
Rad54l |
A |
G |
4: 115,967,906 (GRCm39) |
V152A |
possibly damaging |
Het |
Ranbp2 |
T |
A |
10: 58,318,909 (GRCm39) |
Y2473* |
probably null |
Het |
Sertad1 |
T |
C |
7: 27,188,910 (GRCm39) |
I77T |
possibly damaging |
Het |
Sesn3 |
A |
T |
9: 14,219,873 (GRCm39) |
E87D |
probably damaging |
Het |
Slc30a5 |
A |
T |
13: 100,950,477 (GRCm39) |
S260R |
probably benign |
Het |
Slc6a12 |
G |
A |
6: 121,328,972 (GRCm39) |
G111S |
probably damaging |
Het |
Slc6a12 |
T |
C |
6: 121,328,978 (GRCm39) |
Y113H |
probably benign |
Het |
Spag17 |
T |
G |
3: 99,847,299 (GRCm39) |
M76R |
probably benign |
Het |
Spata31f3 |
TCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGTCATTCAACACTTTGG |
TCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGTCATTCAACACTTTGG |
4: 42,871,823 (GRCm39) |
|
probably benign |
Het |
Stard13 |
G |
A |
5: 150,986,038 (GRCm39) |
Q491* |
probably null |
Het |
Synpo2 |
T |
C |
3: 122,910,968 (GRCm39) |
S226G |
probably benign |
Het |
Tada2b |
G |
A |
5: 36,641,331 (GRCm39) |
T24I |
probably benign |
Het |
Tafa1 |
T |
C |
6: 96,092,737 (GRCm39) |
|
probably null |
Het |
Tmem51 |
TCCCC |
TCCC |
4: 141,764,996 (GRCm39) |
|
probably null |
Het |
Tnnt1 |
T |
A |
7: 4,513,547 (GRCm39) |
|
probably null |
Het |
Usp17lb |
T |
C |
7: 104,490,340 (GRCm39) |
I196V |
probably benign |
Het |
Utp20 |
T |
A |
10: 88,649,811 (GRCm39) |
K466N |
possibly damaging |
Het |
Wdr46 |
T |
C |
17: 34,160,859 (GRCm39) |
|
probably null |
Het |
Zfp287 |
T |
A |
11: 62,605,104 (GRCm39) |
Q601L |
probably damaging |
Het |
Zfp410 |
T |
C |
12: 84,372,464 (GRCm39) |
S97P |
probably benign |
Het |
|
Other mutations in Ghsr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00264:Ghsr
|
APN |
3 |
27,429,022 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00435:Ghsr
|
APN |
3 |
27,426,532 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01376:Ghsr
|
APN |
3 |
27,425,977 (GRCm39) |
missense |
probably benign |
|
IGL02444:Ghsr
|
APN |
3 |
27,426,189 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02650:Ghsr
|
APN |
3 |
27,429,004 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02754:Ghsr
|
APN |
3 |
27,426,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R0571:Ghsr
|
UTSW |
3 |
27,426,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R0825:Ghsr
|
UTSW |
3 |
27,428,776 (GRCm39) |
missense |
probably damaging |
0.99 |
R1036:Ghsr
|
UTSW |
3 |
27,428,869 (GRCm39) |
missense |
probably damaging |
0.98 |
R1462:Ghsr
|
UTSW |
3 |
27,426,025 (GRCm39) |
missense |
probably benign |
0.01 |
R1462:Ghsr
|
UTSW |
3 |
27,426,025 (GRCm39) |
missense |
probably benign |
0.01 |
R1529:Ghsr
|
UTSW |
3 |
27,426,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R1598:Ghsr
|
UTSW |
3 |
27,426,426 (GRCm39) |
missense |
probably benign |
0.27 |
R4846:Ghsr
|
UTSW |
3 |
27,425,986 (GRCm39) |
missense |
probably benign |
|
R4951:Ghsr
|
UTSW |
3 |
27,426,510 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4993:Ghsr
|
UTSW |
3 |
27,426,403 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5055:Ghsr
|
UTSW |
3 |
27,426,421 (GRCm39) |
missense |
probably benign |
0.28 |
R6843:Ghsr
|
UTSW |
3 |
27,426,676 (GRCm39) |
missense |
probably benign |
|
R6936:Ghsr
|
UTSW |
3 |
27,426,474 (GRCm39) |
missense |
probably benign |
0.02 |
R7068:Ghsr
|
UTSW |
3 |
27,425,986 (GRCm39) |
missense |
probably benign |
0.01 |
R7510:Ghsr
|
UTSW |
3 |
27,426,523 (GRCm39) |
missense |
probably benign |
0.05 |
R7889:Ghsr
|
UTSW |
3 |
27,426,315 (GRCm39) |
missense |
probably benign |
0.00 |
R9514:Ghsr
|
UTSW |
3 |
27,426,630 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9571:Ghsr
|
UTSW |
3 |
27,426,664 (GRCm39) |
missense |
probably benign |
0.00 |
R9741:Ghsr
|
UTSW |
3 |
27,428,898 (GRCm39) |
missense |
possibly damaging |
0.85 |
|