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 |
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 |
Sox2 |
G |
A |
3: 34,705,075 (GRCm39) |
G171S |
possibly 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 Mtus1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00708:Mtus1
|
APN |
8 |
41,537,386 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01377:Mtus1
|
APN |
8 |
41,536,172 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01472:Mtus1
|
APN |
8 |
41,455,449 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01995:Mtus1
|
APN |
8 |
41,537,457 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02027:Mtus1
|
APN |
8 |
41,446,638 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02381:Mtus1
|
APN |
8 |
41,536,156 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02571:Mtus1
|
APN |
8 |
41,536,519 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02936:Mtus1
|
APN |
8 |
41,452,554 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0116:Mtus1
|
UTSW |
8 |
41,451,514 (GRCm39) |
unclassified |
probably benign |
|
R0139:Mtus1
|
UTSW |
8 |
41,469,233 (GRCm39) |
splice site |
probably benign |
|
R0178:Mtus1
|
UTSW |
8 |
41,455,398 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0179:Mtus1
|
UTSW |
8 |
41,455,398 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0220:Mtus1
|
UTSW |
8 |
41,447,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R0324:Mtus1
|
UTSW |
8 |
41,537,432 (GRCm39) |
missense |
probably benign |
|
R0355:Mtus1
|
UTSW |
8 |
41,535,965 (GRCm39) |
missense |
probably benign |
0.02 |
R0357:Mtus1
|
UTSW |
8 |
41,536,563 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0464:Mtus1
|
UTSW |
8 |
41,455,511 (GRCm39) |
missense |
probably damaging |
0.96 |
R0681:Mtus1
|
UTSW |
8 |
41,446,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R1016:Mtus1
|
UTSW |
8 |
41,503,063 (GRCm39) |
missense |
probably benign |
0.43 |
R1570:Mtus1
|
UTSW |
8 |
41,529,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Mtus1
|
UTSW |
8 |
41,535,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R1607:Mtus1
|
UTSW |
8 |
41,468,446 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1869:Mtus1
|
UTSW |
8 |
41,529,267 (GRCm39) |
critical splice donor site |
probably null |
|
R1888:Mtus1
|
UTSW |
8 |
41,537,362 (GRCm39) |
missense |
probably damaging |
0.96 |
R1888:Mtus1
|
UTSW |
8 |
41,537,362 (GRCm39) |
missense |
probably damaging |
0.96 |
R1891:Mtus1
|
UTSW |
8 |
41,537,362 (GRCm39) |
missense |
probably damaging |
0.96 |
R1894:Mtus1
|
UTSW |
8 |
41,537,362 (GRCm39) |
missense |
probably damaging |
0.96 |
R2063:Mtus1
|
UTSW |
8 |
41,535,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Mtus1
|
UTSW |
8 |
41,475,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R2112:Mtus1
|
UTSW |
8 |
41,475,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R2224:Mtus1
|
UTSW |
8 |
41,535,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R2226:Mtus1
|
UTSW |
8 |
41,535,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R2227:Mtus1
|
UTSW |
8 |
41,535,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R2516:Mtus1
|
UTSW |
8 |
41,535,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R3414:Mtus1
|
UTSW |
8 |
41,501,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R3899:Mtus1
|
UTSW |
8 |
41,536,166 (GRCm39) |
missense |
probably benign |
|
R4096:Mtus1
|
UTSW |
8 |
41,537,284 (GRCm39) |
missense |
probably damaging |
0.99 |
R4831:Mtus1
|
UTSW |
8 |
41,536,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850:Mtus1
|
UTSW |
8 |
41,537,507 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4916:Mtus1
|
UTSW |
8 |
41,453,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R4940:Mtus1
|
UTSW |
8 |
41,494,515 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4988:Mtus1
|
UTSW |
8 |
41,537,578 (GRCm39) |
missense |
probably benign |
0.05 |
R5133:Mtus1
|
UTSW |
8 |
41,536,229 (GRCm39) |
missense |
probably benign |
0.00 |
R5468:Mtus1
|
UTSW |
8 |
41,537,615 (GRCm39) |
missense |
probably benign |
0.00 |
R5598:Mtus1
|
UTSW |
8 |
41,475,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5782:Mtus1
|
UTSW |
8 |
41,535,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R5860:Mtus1
|
UTSW |
8 |
41,529,303 (GRCm39) |
missense |
probably damaging |
0.99 |
R5900:Mtus1
|
UTSW |
8 |
41,536,534 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5943:Mtus1
|
UTSW |
8 |
41,537,302 (GRCm39) |
missense |
probably benign |
0.00 |
R6019:Mtus1
|
UTSW |
8 |
41,536,077 (GRCm39) |
missense |
probably benign |
0.33 |
R6125:Mtus1
|
UTSW |
8 |
41,537,576 (GRCm39) |
missense |
probably damaging |
0.99 |
R6197:Mtus1
|
UTSW |
8 |
41,537,074 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6488:Mtus1
|
UTSW |
8 |
41,494,545 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6869:Mtus1
|
UTSW |
8 |
41,535,691 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7126:Mtus1
|
UTSW |
8 |
41,468,439 (GRCm39) |
missense |
probably damaging |
0.98 |
R7213:Mtus1
|
UTSW |
8 |
41,537,524 (GRCm39) |
missense |
probably damaging |
0.99 |
R7308:Mtus1
|
UTSW |
8 |
41,535,965 (GRCm39) |
missense |
probably benign |
0.02 |
R7424:Mtus1
|
UTSW |
8 |
41,475,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R7481:Mtus1
|
UTSW |
8 |
41,537,652 (GRCm39) |
missense |
probably damaging |
0.99 |
R7485:Mtus1
|
UTSW |
8 |
41,537,590 (GRCm39) |
missense |
probably benign |
0.37 |
R7660:Mtus1
|
UTSW |
8 |
41,469,248 (GRCm39) |
missense |
probably benign |
|
R7699:Mtus1
|
UTSW |
8 |
41,537,006 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7700:Mtus1
|
UTSW |
8 |
41,537,006 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7709:Mtus1
|
UTSW |
8 |
41,507,687 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7791:Mtus1
|
UTSW |
8 |
41,536,417 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8196:Mtus1
|
UTSW |
8 |
41,509,689 (GRCm39) |
missense |
probably benign |
|
R8463:Mtus1
|
UTSW |
8 |
41,536,271 (GRCm39) |
missense |
probably benign |
0.01 |
R8724:Mtus1
|
UTSW |
8 |
41,451,500 (GRCm39) |
missense |
probably damaging |
0.99 |
R9047:Mtus1
|
UTSW |
8 |
41,536,760 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9092:Mtus1
|
UTSW |
8 |
41,455,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R9283:Mtus1
|
UTSW |
8 |
41,536,519 (GRCm39) |
missense |
probably benign |
0.02 |
R9313:Mtus1
|
UTSW |
8 |
41,535,923 (GRCm39) |
missense |
probably damaging |
0.99 |
R9329:Mtus1
|
UTSW |
8 |
41,537,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R9603:Mtus1
|
UTSW |
8 |
41,536,795 (GRCm39) |
missense |
probably benign |
0.04 |
R9711:Mtus1
|
UTSW |
8 |
41,536,222 (GRCm39) |
missense |
probably damaging |
0.99 |
|