Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
T |
C |
5: 113,339,250 (GRCm39) |
Y254C |
probably benign |
Het |
4930480E11Rik |
G |
T |
X: 77,414,311 (GRCm39) |
M345I |
probably benign |
Het |
Adam12 |
T |
C |
7: 133,518,191 (GRCm39) |
I650V |
probably benign |
Het |
Adam39 |
G |
T |
8: 41,279,279 (GRCm39) |
G557C |
probably damaging |
Het |
Ak5 |
A |
G |
3: 152,321,493 (GRCm39) |
|
probably null |
Het |
Arhgef10l |
C |
T |
4: 140,291,497 (GRCm39) |
|
probably null |
Het |
Arhgef37 |
C |
T |
18: 61,637,481 (GRCm39) |
E394K |
probably benign |
Het |
Baz2b |
A |
G |
2: 59,742,841 (GRCm39) |
V13A |
|
Het |
Bnc1 |
G |
T |
7: 81,623,109 (GRCm39) |
A706E |
possibly damaging |
Het |
Bscl2 |
G |
A |
19: 8,825,878 (GRCm39) |
A421T |
possibly damaging |
Het |
Btn1a1 |
A |
C |
13: 23,643,415 (GRCm39) |
W345G |
possibly damaging |
Het |
C3 |
A |
T |
17: 57,519,655 (GRCm39) |
M1199K |
probably benign |
Het |
Ccdc18 |
T |
G |
5: 108,296,835 (GRCm39) |
L213V |
possibly damaging |
Het |
Cers2 |
T |
C |
3: 95,228,072 (GRCm39) |
|
probably null |
Het |
Chpt1 |
T |
A |
10: 88,316,711 (GRCm39) |
H249L |
probably damaging |
Het |
Cited2 |
A |
G |
10: 17,600,364 (GRCm39) |
E224G |
possibly damaging |
Het |
Cntn5 |
T |
A |
9: 10,904,704 (GRCm39) |
|
probably benign |
Het |
Col28a1 |
A |
G |
6: 8,013,122 (GRCm39) |
S977P |
possibly damaging |
Het |
Col6a1 |
T |
C |
10: 76,560,843 (GRCm39) |
K52E |
probably damaging |
Het |
Cpne2 |
T |
A |
8: 95,282,172 (GRCm39) |
H239Q |
probably damaging |
Het |
Cr2 |
A |
T |
1: 194,842,909 (GRCm39) |
N244K |
possibly damaging |
Het |
Csf2rb2 |
T |
C |
15: 78,169,385 (GRCm39) |
D590G |
probably damaging |
Het |
Defb25 |
A |
C |
2: 152,464,380 (GRCm39) |
C55G |
probably damaging |
Het |
Dnah7b |
A |
T |
1: 46,391,973 (GRCm39) |
|
probably null |
Het |
Dvl3 |
T |
A |
16: 20,346,072 (GRCm39) |
Y467* |
probably null |
Het |
Elapor2 |
T |
A |
5: 9,495,384 (GRCm39) |
C729* |
probably null |
Het |
Extl2 |
T |
C |
3: 115,821,088 (GRCm39) |
S312P |
probably damaging |
Het |
Fam178b |
T |
C |
1: 36,639,548 (GRCm39) |
T313A |
probably benign |
Het |
Fam186b |
A |
G |
15: 99,183,471 (GRCm39) |
Y58H |
probably damaging |
Het |
Fat1 |
A |
T |
8: 45,484,505 (GRCm39) |
I3248L |
probably damaging |
Het |
Fat2 |
A |
G |
11: 55,172,088 (GRCm39) |
F2875S |
probably damaging |
Het |
Flnb |
T |
A |
14: 7,894,214 (GRCm38) |
N760K |
probably benign |
Het |
Galnt14 |
T |
C |
17: 73,801,190 (GRCm39) |
H544R |
probably benign |
Het |
Gpr137c |
A |
C |
14: 45,516,484 (GRCm39) |
R357S |
probably damaging |
Het |
Grk2 |
A |
G |
19: 4,340,630 (GRCm39) |
|
probably null |
Het |
Hectd2 |
A |
T |
19: 36,577,055 (GRCm39) |
T342S |
probably benign |
Het |
Hjv |
G |
T |
3: 96,435,542 (GRCm39) |
V267L |
possibly damaging |
Het |
Ildr2 |
G |
T |
1: 166,123,380 (GRCm39) |
G270C |
probably damaging |
Het |
Insm2 |
C |
A |
12: 55,647,357 (GRCm39) |
A367D |
probably damaging |
Het |
Kcnh5 |
T |
A |
12: 75,161,219 (GRCm39) |
I230F |
possibly damaging |
Het |
Keg1 |
T |
A |
19: 12,687,042 (GRCm39) |
S24T |
probably damaging |
Het |
Kera |
A |
T |
10: 97,448,714 (GRCm39) |
E311D |
probably benign |
Het |
Kit |
T |
A |
5: 75,767,758 (GRCm39) |
I47K |
probably benign |
Het |
Megf6 |
A |
G |
4: 154,343,379 (GRCm39) |
T663A |
possibly damaging |
Het |
Mettl21c |
G |
A |
1: 44,049,808 (GRCm39) |
A79V |
probably damaging |
Het |
Mfsd1 |
T |
A |
3: 67,507,391 (GRCm39) |
|
probably null |
Het |
Mob3b |
A |
G |
4: 34,985,914 (GRCm39) |
|
probably null |
Het |
Morc2b |
T |
A |
17: 33,356,926 (GRCm39) |
H282L |
probably benign |
Het |
Mtpap |
T |
C |
18: 4,380,889 (GRCm39) |
|
probably null |
Het |
Mtus1 |
A |
G |
8: 41,536,621 (GRCm39) |
V365A |
possibly damaging |
Het |
Muc5ac |
T |
A |
7: 141,367,559 (GRCm39) |
Y2993* |
probably null |
Het |
Mycbp2 |
A |
C |
14: 103,391,513 (GRCm39) |
F3422V |
probably benign |
Het |
Ndufb7 |
T |
A |
8: 84,297,490 (GRCm39) |
D48E |
probably benign |
Het |
Nxpe5 |
A |
G |
5: 138,237,704 (GRCm39) |
Y88C |
probably damaging |
Het |
Or51a6 |
T |
A |
7: 102,604,185 (GRCm39) |
M208L |
probably benign |
Het |
Or5d3 |
A |
G |
2: 88,174,905 (GRCm39) |
L64P |
probably damaging |
Het |
Osbpl5 |
T |
A |
7: 143,263,520 (GRCm39) |
D121V |
probably benign |
Het |
Oxnad1 |
A |
T |
14: 31,813,608 (GRCm39) |
H3L |
probably benign |
Het |
Pam |
C |
A |
1: 97,904,841 (GRCm39) |
|
probably benign |
Het |
Papolg |
T |
C |
11: 23,845,207 (GRCm39) |
|
probably benign |
Het |
Pax1 |
G |
A |
2: 147,208,190 (GRCm39) |
G266D |
probably damaging |
Het |
Pde11a |
A |
T |
2: 75,906,348 (GRCm39) |
M623K |
probably damaging |
Het |
Peg3 |
GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC |
GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC |
7: 6,712,167 (GRCm39) |
|
probably benign |
Het |
Phf21a |
A |
T |
2: 92,189,502 (GRCm39) |
Q587L |
probably benign |
Het |
Plcb3 |
A |
G |
19: 6,941,746 (GRCm39) |
L336P |
probably damaging |
Het |
Pnp2 |
T |
C |
14: 51,201,931 (GRCm39) |
*306Q |
probably null |
Het |
Pou5f2 |
A |
G |
13: 78,173,392 (GRCm39) |
I111M |
probably benign |
Het |
Pramel32 |
T |
A |
4: 88,547,195 (GRCm39) |
M246L |
probably damaging |
Het |
Prmt3 |
G |
T |
7: 49,467,843 (GRCm39) |
A350S |
probably benign |
Het |
Rac3 |
A |
T |
11: 120,614,343 (GRCm39) |
R163* |
probably null |
Het |
Raly |
G |
T |
2: 154,699,432 (GRCm39) |
V79L |
probably benign |
Het |
Rbm20 |
A |
T |
19: 53,839,989 (GRCm39) |
T993S |
possibly damaging |
Het |
Rwdd3 |
A |
G |
3: 120,964,987 (GRCm39) |
L56P |
probably benign |
Het |
Serpina3a |
C |
T |
12: 104,082,436 (GRCm39) |
H70Y |
possibly damaging |
Het |
Sez6l2 |
A |
C |
7: 126,552,915 (GRCm39) |
E227A |
possibly damaging |
Het |
Shank1 |
C |
T |
7: 43,976,585 (GRCm39) |
A561V |
unknown |
Het |
Sidt2 |
C |
T |
9: 45,864,517 (GRCm39) |
V71I |
probably benign |
Het |
Slc35f6 |
T |
C |
5: 30,815,051 (GRCm39) |
L326P |
probably damaging |
Het |
Spef2 |
G |
A |
15: 9,729,924 (GRCm39) |
R65C |
probably damaging |
Het |
Spmap2 |
A |
T |
10: 79,420,741 (GRCm39) |
|
probably null |
Het |
Stip1 |
C |
T |
19: 6,999,178 (GRCm39) |
G467S |
possibly damaging |
Het |
Tada2a |
T |
A |
11: 83,976,514 (GRCm39) |
I327F |
probably damaging |
Het |
Tex2 |
A |
G |
11: 106,435,071 (GRCm39) |
V785A |
unknown |
Het |
Thada |
C |
A |
17: 84,538,214 (GRCm39) |
|
probably null |
Het |
Tmed1 |
G |
A |
9: 21,420,550 (GRCm39) |
T94M |
possibly damaging |
Het |
Tsr1 |
G |
T |
11: 74,790,360 (GRCm39) |
M149I |
probably benign |
Het |
Ttc8 |
T |
C |
12: 98,942,761 (GRCm39) |
Y434H |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,578,519 (GRCm39) |
Y24125H |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,552,253 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
G |
2: 76,773,235 (GRCm39) |
I2435T |
unknown |
Het |
Uggt2 |
T |
C |
14: 119,251,938 (GRCm39) |
I1174M |
probably benign |
Het |
Unc13b |
T |
C |
4: 43,216,544 (GRCm39) |
I281T |
probably benign |
Het |
Usp1 |
G |
T |
4: 98,817,127 (GRCm39) |
K106N |
possibly damaging |
Het |
Vwa3b |
A |
G |
1: 37,174,634 (GRCm39) |
D15G |
|
Het |
Zfp28 |
G |
A |
7: 6,397,461 (GRCm39) |
C632Y |
probably damaging |
Het |
Zfp68 |
T |
C |
5: 138,604,580 (GRCm39) |
D581G |
probably benign |
Het |
Zmynd10 |
A |
C |
9: 107,424,716 (GRCm39) |
S21R |
probably benign |
Het |
Zswim4 |
C |
T |
8: 84,940,681 (GRCm39) |
R806H |
probably damaging |
Het |
|
Other mutations in Sox2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02578:Sox2
|
APN |
3 |
34,704,745 (GRCm39) |
missense |
probably benign |
0.37 |
IGL03397:Sox2
|
APN |
3 |
34,704,686 (GRCm39) |
missense |
probably damaging |
0.99 |
R1164:Sox2
|
UTSW |
3 |
34,704,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R1667:Sox2
|
UTSW |
3 |
34,704,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R1829:Sox2
|
UTSW |
3 |
34,704,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R1925:Sox2
|
UTSW |
3 |
34,704,820 (GRCm39) |
nonsense |
probably null |
|
R2066:Sox2
|
UTSW |
3 |
34,705,456 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4170:Sox2
|
UTSW |
3 |
34,704,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R4585:Sox2
|
UTSW |
3 |
34,705,193 (GRCm39) |
missense |
probably benign |
0.02 |
R4586:Sox2
|
UTSW |
3 |
34,705,193 (GRCm39) |
missense |
probably benign |
0.02 |
R4703:Sox2
|
UTSW |
3 |
34,704,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R5509:Sox2
|
UTSW |
3 |
34,704,938 (GRCm39) |
missense |
probably damaging |
0.98 |
R5549:Sox2
|
UTSW |
3 |
34,705,142 (GRCm39) |
missense |
probably benign |
0.01 |
R5637:Sox2
|
UTSW |
3 |
34,704,677 (GRCm39) |
missense |
probably benign |
0.03 |
R6494:Sox2
|
UTSW |
3 |
34,705,246 (GRCm39) |
missense |
probably benign |
0.01 |
R7210:Sox2
|
UTSW |
3 |
34,705,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R7365:Sox2
|
UTSW |
3 |
34,705,121 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7798:Sox2
|
UTSW |
3 |
34,704,791 (GRCm39) |
missense |
probably damaging |
0.96 |
R7801:Sox2
|
UTSW |
3 |
34,704,791 (GRCm39) |
missense |
probably damaging |
0.96 |
R8684:Sox2
|
UTSW |
3 |
34,705,016 (GRCm39) |
missense |
probably benign |
0.00 |
R8889:Sox2
|
UTSW |
3 |
34,705,129 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9013:Sox2
|
UTSW |
3 |
34,704,746 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:Sox2
|
UTSW |
3 |
34,704,838 (GRCm39) |
missense |
probably damaging |
1.00 |
|