Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam22 |
A |
G |
5: 8,167,587 (GRCm39) |
|
probably null |
Het |
Agrn |
C |
A |
4: 156,279,854 (GRCm39) |
D106Y |
probably damaging |
Het |
Arfgap3 |
A |
T |
15: 83,192,352 (GRCm39) |
Y416N |
probably benign |
Het |
Atp6v0a2 |
C |
T |
5: 124,775,533 (GRCm39) |
T135M |
probably damaging |
Het |
Bach1 |
C |
A |
16: 87,515,736 (GRCm39) |
Y92* |
probably null |
Het |
Catsperg1 |
A |
C |
7: 28,884,907 (GRCm39) |
C905G |
probably null |
Het |
Cbr2 |
T |
C |
11: 120,620,628 (GRCm39) |
I219V |
probably benign |
Het |
Ccdc3 |
A |
T |
2: 5,233,908 (GRCm39) |
K244I |
probably damaging |
Het |
Cd226 |
T |
C |
18: 89,265,433 (GRCm39) |
V237A |
probably damaging |
Het |
Chek2 |
T |
C |
5: 110,989,319 (GRCm39) |
C81R |
probably benign |
Het |
Col27a1 |
T |
C |
4: 63,242,723 (GRCm39) |
|
probably null |
Het |
Cracdl |
T |
A |
1: 37,663,858 (GRCm39) |
Q680L |
probably benign |
Het |
Crybg3 |
A |
T |
16: 59,379,236 (GRCm39) |
S673T |
probably benign |
Het |
Csmd2 |
T |
A |
4: 128,276,743 (GRCm39) |
Y848* |
probably null |
Het |
Dgkb |
C |
A |
12: 38,680,592 (GRCm39) |
T764K |
probably damaging |
Het |
Dock4 |
T |
A |
12: 40,775,648 (GRCm39) |
C530* |
probably null |
Het |
Dpyd |
A |
G |
3: 118,597,780 (GRCm39) |
K254R |
probably benign |
Het |
Dstyk |
C |
T |
1: 132,384,614 (GRCm39) |
P703S |
possibly damaging |
Het |
Ehhadh |
A |
T |
16: 21,585,140 (GRCm39) |
I247N |
probably damaging |
Het |
Fer1l5 |
T |
G |
1: 36,440,558 (GRCm39) |
L597R |
probably damaging |
Het |
Fignl1 |
T |
C |
11: 11,752,842 (GRCm39) |
E71G |
probably damaging |
Het |
Fnip2 |
A |
C |
3: 79,425,421 (GRCm39) |
V58G |
probably damaging |
Het |
Gapdhs |
A |
T |
7: 30,431,349 (GRCm39) |
I377N |
probably damaging |
Het |
Gcn1 |
C |
T |
5: 115,733,359 (GRCm39) |
A1059V |
probably damaging |
Het |
Gpd1 |
G |
A |
15: 99,619,967 (GRCm39) |
S255N |
probably damaging |
Het |
Grik2 |
A |
C |
10: 49,295,792 (GRCm39) |
I392S |
probably damaging |
Het |
Hoxb3 |
T |
C |
11: 96,236,606 (GRCm39) |
L228P |
probably damaging |
Het |
Iws1 |
A |
T |
18: 32,223,568 (GRCm39) |
M659L |
probably benign |
Het |
Kmt2c |
A |
G |
5: 25,580,364 (GRCm39) |
C570R |
probably benign |
Het |
Lamc3 |
T |
A |
2: 31,812,279 (GRCm39) |
|
probably null |
Het |
Lipf |
G |
A |
19: 33,943,048 (GRCm39) |
G119R |
probably damaging |
Het |
Lrrc37 |
T |
C |
11: 103,507,719 (GRCm39) |
I1416M |
unknown |
Het |
Magel2 |
A |
T |
7: 62,028,130 (GRCm39) |
I345L |
probably benign |
Het |
Mdn1 |
G |
A |
4: 32,722,360 (GRCm39) |
A2381T |
possibly damaging |
Het |
Med12l |
T |
C |
3: 59,001,007 (GRCm39) |
V690A |
probably benign |
Het |
Megf10 |
GGCAGCAACAGCACCAGCAGCAACAGCACCAGCAGCA |
GGCAGCAACAGCACCAGCAGCA |
18: 57,427,071 (GRCm39) |
|
probably benign |
Het |
Mob3b |
A |
G |
4: 35,083,872 (GRCm39) |
Y106H |
probably damaging |
Het |
Myo1c |
T |
C |
11: 75,549,519 (GRCm39) |
Y166H |
probably damaging |
Het |
Ndst4 |
A |
T |
3: 125,364,493 (GRCm39) |
H390L |
probably benign |
Het |
Nt5c1b |
T |
A |
12: 10,425,472 (GRCm39) |
N280K |
probably damaging |
Het |
Or10aa1 |
G |
A |
1: 173,869,900 (GRCm39) |
R128H |
probably benign |
Het |
Or5b116 |
A |
T |
19: 13,423,252 (GRCm39) |
N292I |
probably damaging |
Het |
Pabpc4 |
G |
A |
4: 123,189,102 (GRCm39) |
A481T |
probably benign |
Het |
Parm1 |
C |
T |
5: 91,741,791 (GRCm39) |
T53I |
possibly damaging |
Het |
Pilra |
C |
T |
5: 137,833,679 (GRCm39) |
R129Q |
probably benign |
Het |
Pkd1 |
C |
T |
17: 24,769,250 (GRCm39) |
A5V |
unknown |
Het |
Pmch |
T |
C |
10: 87,927,242 (GRCm39) |
S82P |
probably benign |
Het |
Prf1 |
G |
A |
10: 61,135,934 (GRCm39) |
R70H |
possibly damaging |
Het |
Rad51c |
T |
C |
11: 87,292,276 (GRCm39) |
S180G |
probably benign |
Het |
Rassf8 |
A |
C |
6: 145,760,973 (GRCm39) |
T100P |
probably damaging |
Het |
Rnpepl1 |
A |
G |
1: 92,844,890 (GRCm39) |
E394G |
probably damaging |
Het |
Rufy2 |
T |
A |
10: 62,838,772 (GRCm39) |
V418E |
probably benign |
Het |
Sdad1 |
A |
T |
5: 92,450,538 (GRCm39) |
V199D |
probably damaging |
Het |
Sptbn4 |
A |
T |
7: 27,063,761 (GRCm39) |
S2227T |
probably benign |
Het |
Tac4 |
A |
G |
11: 95,156,116 (GRCm39) |
M66V |
probably benign |
Het |
Tas2r126 |
T |
C |
6: 42,412,031 (GRCm39) |
V188A |
probably benign |
Het |
Tcerg1 |
T |
C |
18: 42,694,000 (GRCm39) |
V707A |
possibly damaging |
Het |
Tmem273 |
A |
G |
14: 32,527,129 (GRCm39) |
E32G |
possibly damaging |
Het |
Trav13d-4 |
G |
A |
14: 53,995,355 (GRCm39) |
G103D |
probably damaging |
Het |
Trav8d-1 |
A |
G |
14: 53,016,380 (GRCm39) |
S89G |
probably benign |
Het |
Ttll4 |
C |
T |
1: 74,718,572 (GRCm39) |
S141L |
probably benign |
Het |
Vash1 |
T |
C |
12: 86,738,614 (GRCm39) |
S354P |
probably benign |
Het |
Vmn2r40 |
T |
A |
7: 8,911,116 (GRCm39) |
I726F |
|
Het |
Vmn2r53 |
A |
C |
7: 12,340,418 (GRCm39) |
N18K |
probably damaging |
Het |
Wnt6 |
T |
C |
1: 74,823,422 (GRCm39) |
F253S |
probably damaging |
Het |
Zfp599 |
A |
G |
9: 22,161,811 (GRCm39) |
I118T |
probably benign |
Het |
|
Other mutations in Otof |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Otof
|
APN |
5 |
30,533,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00391:Otof
|
APN |
5 |
30,532,967 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00579:Otof
|
APN |
5 |
30,556,666 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00671:Otof
|
APN |
5 |
30,543,097 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01019:Otof
|
APN |
5 |
30,562,560 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01025:Otof
|
APN |
5 |
30,541,597 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01086:Otof
|
APN |
5 |
30,533,617 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01110:Otof
|
APN |
5 |
30,619,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01160:Otof
|
APN |
5 |
30,538,879 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01285:Otof
|
APN |
5 |
30,562,527 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01329:Otof
|
APN |
5 |
30,598,723 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01337:Otof
|
APN |
5 |
30,576,856 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01337:Otof
|
APN |
5 |
30,563,121 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01834:Otof
|
APN |
5 |
30,556,564 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01872:Otof
|
APN |
5 |
30,536,598 (GRCm39) |
splice site |
probably benign |
|
IGL01969:Otof
|
APN |
5 |
30,539,827 (GRCm39) |
splice site |
probably benign |
|
IGL02075:Otof
|
APN |
5 |
30,528,070 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02077:Otof
|
APN |
5 |
30,556,579 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02136:Otof
|
APN |
5 |
30,531,336 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02227:Otof
|
APN |
5 |
30,528,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02475:Otof
|
APN |
5 |
30,534,026 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02812:Otof
|
APN |
5 |
30,531,426 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02864:Otof
|
APN |
5 |
30,543,685 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03176:Otof
|
APN |
5 |
30,562,520 (GRCm39) |
splice site |
probably null |
|
R0285:Otof
|
UTSW |
5 |
30,536,877 (GRCm39) |
critical splice donor site |
probably null |
|
R0421:Otof
|
UTSW |
5 |
30,528,912 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0570:Otof
|
UTSW |
5 |
30,529,225 (GRCm39) |
splice site |
probably benign |
|
R0599:Otof
|
UTSW |
5 |
30,528,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Otof
|
UTSW |
5 |
30,539,705 (GRCm39) |
missense |
probably benign |
0.01 |
R0715:Otof
|
UTSW |
5 |
30,552,041 (GRCm39) |
missense |
probably damaging |
0.99 |
R1019:Otof
|
UTSW |
5 |
30,528,087 (GRCm39) |
missense |
probably damaging |
0.96 |
R1183:Otof
|
UTSW |
5 |
30,529,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1435:Otof
|
UTSW |
5 |
30,536,039 (GRCm39) |
missense |
probably benign |
0.00 |
R1469:Otof
|
UTSW |
5 |
30,537,571 (GRCm39) |
missense |
probably benign |
0.00 |
R1469:Otof
|
UTSW |
5 |
30,537,571 (GRCm39) |
missense |
probably benign |
0.00 |
R1474:Otof
|
UTSW |
5 |
30,536,876 (GRCm39) |
critical splice donor site |
probably null |
|
R1524:Otof
|
UTSW |
5 |
30,536,900 (GRCm39) |
missense |
probably benign |
0.03 |
R1563:Otof
|
UTSW |
5 |
30,528,349 (GRCm39) |
missense |
probably benign |
0.00 |
R1732:Otof
|
UTSW |
5 |
30,543,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Otof
|
UTSW |
5 |
30,536,054 (GRCm39) |
missense |
probably benign |
0.00 |
R1845:Otof
|
UTSW |
5 |
30,529,067 (GRCm39) |
nonsense |
probably null |
|
R1925:Otof
|
UTSW |
5 |
30,551,532 (GRCm39) |
missense |
probably benign |
0.37 |
R1938:Otof
|
UTSW |
5 |
30,533,713 (GRCm39) |
missense |
probably benign |
0.00 |
R1968:Otof
|
UTSW |
5 |
30,545,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R1996:Otof
|
UTSW |
5 |
30,578,381 (GRCm39) |
missense |
probably benign |
0.01 |
R1999:Otof
|
UTSW |
5 |
30,546,116 (GRCm39) |
missense |
probably benign |
0.19 |
R2027:Otof
|
UTSW |
5 |
30,578,358 (GRCm39) |
missense |
probably benign |
0.08 |
R2138:Otof
|
UTSW |
5 |
30,619,114 (GRCm39) |
missense |
probably benign |
0.01 |
R2173:Otof
|
UTSW |
5 |
30,543,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R2245:Otof
|
UTSW |
5 |
30,527,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R3011:Otof
|
UTSW |
5 |
30,540,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R3105:Otof
|
UTSW |
5 |
30,539,145 (GRCm39) |
missense |
probably benign |
0.03 |
R3442:Otof
|
UTSW |
5 |
30,529,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R3710:Otof
|
UTSW |
5 |
30,542,610 (GRCm39) |
missense |
probably benign |
|
R3715:Otof
|
UTSW |
5 |
30,534,215 (GRCm39) |
nonsense |
probably null |
|
R3806:Otof
|
UTSW |
5 |
30,543,843 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3975:Otof
|
UTSW |
5 |
30,528,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R4067:Otof
|
UTSW |
5 |
30,556,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R4077:Otof
|
UTSW |
5 |
30,576,850 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4166:Otof
|
UTSW |
5 |
30,539,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R4451:Otof
|
UTSW |
5 |
30,542,508 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4485:Otof
|
UTSW |
5 |
30,532,344 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4600:Otof
|
UTSW |
5 |
30,529,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4646:Otof
|
UTSW |
5 |
30,540,914 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4648:Otof
|
UTSW |
5 |
30,540,914 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4669:Otof
|
UTSW |
5 |
30,578,318 (GRCm39) |
critical splice donor site |
probably null |
|
R4773:Otof
|
UTSW |
5 |
30,552,026 (GRCm39) |
missense |
probably benign |
0.05 |
R4839:Otof
|
UTSW |
5 |
30,576,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R4907:Otof
|
UTSW |
5 |
30,536,005 (GRCm39) |
critical splice donor site |
probably null |
|
R4961:Otof
|
UTSW |
5 |
30,540,837 (GRCm39) |
intron |
probably benign |
|
R4991:Otof
|
UTSW |
5 |
30,551,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Otof
|
UTSW |
5 |
30,540,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R5036:Otof
|
UTSW |
5 |
30,541,783 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5038:Otof
|
UTSW |
5 |
30,541,783 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5253:Otof
|
UTSW |
5 |
30,527,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R5336:Otof
|
UTSW |
5 |
30,534,064 (GRCm39) |
missense |
probably benign |
0.01 |
R5365:Otof
|
UTSW |
5 |
30,539,144 (GRCm39) |
missense |
probably damaging |
0.99 |
R5901:Otof
|
UTSW |
5 |
30,532,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R6211:Otof
|
UTSW |
5 |
30,529,244 (GRCm39) |
missense |
probably damaging |
0.99 |
R6318:Otof
|
UTSW |
5 |
30,571,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R6331:Otof
|
UTSW |
5 |
30,529,279 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6671:Otof
|
UTSW |
5 |
30,576,877 (GRCm39) |
missense |
probably benign |
|
R6701:Otof
|
UTSW |
5 |
30,528,141 (GRCm39) |
nonsense |
probably null |
|
R6792:Otof
|
UTSW |
5 |
30,532,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R6853:Otof
|
UTSW |
5 |
30,545,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R6940:Otof
|
UTSW |
5 |
30,528,987 (GRCm39) |
missense |
probably damaging |
0.96 |
R7037:Otof
|
UTSW |
5 |
30,538,882 (GRCm39) |
missense |
probably benign |
0.32 |
R7060:Otof
|
UTSW |
5 |
30,545,700 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7089:Otof
|
UTSW |
5 |
30,528,912 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7165:Otof
|
UTSW |
5 |
30,532,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R7178:Otof
|
UTSW |
5 |
30,540,878 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7298:Otof
|
UTSW |
5 |
30,545,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R7393:Otof
|
UTSW |
5 |
30,527,614 (GRCm39) |
missense |
probably benign |
0.45 |
R7397:Otof
|
UTSW |
5 |
30,533,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R7400:Otof
|
UTSW |
5 |
30,542,532 (GRCm39) |
missense |
probably benign |
0.04 |
R7428:Otof
|
UTSW |
5 |
30,547,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R7456:Otof
|
UTSW |
5 |
30,552,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R7505:Otof
|
UTSW |
5 |
30,528,364 (GRCm39) |
missense |
probably benign |
0.00 |
R8002:Otof
|
UTSW |
5 |
30,537,954 (GRCm39) |
missense |
probably benign |
0.10 |
R8032:Otof
|
UTSW |
5 |
30,619,142 (GRCm39) |
start codon destroyed |
probably benign |
0.07 |
R8153:Otof
|
UTSW |
5 |
30,546,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R8158:Otof
|
UTSW |
5 |
30,537,538 (GRCm39) |
missense |
probably benign |
0.37 |
R8159:Otof
|
UTSW |
5 |
30,537,538 (GRCm39) |
missense |
probably benign |
0.37 |
R8441:Otof
|
UTSW |
5 |
30,538,200 (GRCm39) |
missense |
probably damaging |
0.99 |
R8738:Otof
|
UTSW |
5 |
30,545,968 (GRCm39) |
nonsense |
probably null |
|
R8813:Otof
|
UTSW |
5 |
30,540,242 (GRCm39) |
missense |
probably benign |
0.02 |
R8835:Otof
|
UTSW |
5 |
30,528,264 (GRCm39) |
missense |
probably benign |
0.44 |
R8852:Otof
|
UTSW |
5 |
30,529,044 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8869:Otof
|
UTSW |
5 |
30,578,325 (GRCm39) |
missense |
probably benign |
0.08 |
R9029:Otof
|
UTSW |
5 |
30,527,419 (GRCm39) |
critical splice donor site |
probably null |
|
R9031:Otof
|
UTSW |
5 |
30,537,532 (GRCm39) |
missense |
probably benign |
|
R9061:Otof
|
UTSW |
5 |
30,546,001 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9100:Otof
|
UTSW |
5 |
30,539,696 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9121:Otof
|
UTSW |
5 |
30,536,462 (GRCm39) |
missense |
probably benign |
0.04 |
R9188:Otof
|
UTSW |
5 |
30,534,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R9218:Otof
|
UTSW |
5 |
30,542,469 (GRCm39) |
missense |
probably benign |
|
R9280:Otof
|
UTSW |
5 |
30,528,894 (GRCm39) |
missense |
probably damaging |
0.98 |
R9395:Otof
|
UTSW |
5 |
30,532,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R9400:Otof
|
UTSW |
5 |
30,540,863 (GRCm39) |
critical splice donor site |
probably null |
|
R9407:Otof
|
UTSW |
5 |
30,538,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R9616:Otof
|
UTSW |
5 |
30,539,708 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9665:Otof
|
UTSW |
5 |
30,584,895 (GRCm39) |
missense |
probably benign |
0.22 |
R9748:Otof
|
UTSW |
5 |
30,540,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R9783:Otof
|
UTSW |
5 |
30,536,576 (GRCm39) |
missense |
probably benign |
|
Z1176:Otof
|
UTSW |
5 |
30,528,930 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Otof
|
UTSW |
5 |
30,541,002 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Otof
|
UTSW |
5 |
30,533,641 (GRCm39) |
missense |
probably damaging |
1.00 |
|