Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001J03Rik |
A |
T |
5: 146,119,343 (GRCm39) |
|
probably benign |
Het |
5730409E04Rik |
A |
G |
4: 126,505,742 (GRCm39) |
E90G |
probably damaging |
Het |
Abhd6 |
T |
A |
14: 8,039,849 (GRCm38) |
I27N |
probably damaging |
Het |
Akap6 |
A |
T |
12: 53,186,277 (GRCm39) |
E1230D |
probably benign |
Het |
Bcl2l12 |
A |
G |
7: 44,646,317 (GRCm39) |
V31A |
possibly damaging |
Het |
Cep350 |
G |
A |
1: 155,738,341 (GRCm39) |
R2501W |
probably damaging |
Het |
Cnga3 |
A |
G |
1: 37,297,072 (GRCm39) |
|
probably null |
Het |
Crcp |
T |
C |
5: 130,088,699 (GRCm39) |
|
probably benign |
Het |
Creb5 |
G |
A |
6: 53,670,909 (GRCm39) |
S304N |
probably damaging |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,219,296 (GRCm39) |
D38G |
probably benign |
Het |
Fam171a1 |
A |
G |
2: 3,224,527 (GRCm39) |
I293V |
possibly damaging |
Het |
Fbxw10 |
T |
C |
11: 62,748,561 (GRCm39) |
V396A |
possibly damaging |
Het |
Gm10340 |
G |
A |
14: 14,832,274 (GRCm39) |
|
probably benign |
Het |
Grik3 |
A |
G |
4: 125,544,310 (GRCm39) |
T344A |
probably benign |
Het |
Itga7 |
T |
C |
10: 128,769,958 (GRCm39) |
F34S |
probably damaging |
Het |
Musk |
T |
C |
4: 58,353,936 (GRCm39) |
|
probably benign |
Het |
Neb |
G |
T |
2: 52,182,831 (GRCm39) |
N1038K |
probably damaging |
Het |
Nf1 |
T |
C |
11: 79,426,493 (GRCm39) |
Y1636H |
probably damaging |
Het |
Ngef |
G |
T |
1: 87,406,872 (GRCm39) |
T632K |
possibly damaging |
Het |
Nme1nme2 |
A |
G |
11: 93,846,400 (GRCm39) |
V16A |
probably damaging |
Het |
Nts |
A |
G |
10: 102,326,108 (GRCm39) |
|
probably benign |
Het |
Olfml2b |
A |
G |
1: 170,509,743 (GRCm39) |
D697G |
probably damaging |
Het |
Or5ac23 |
A |
T |
16: 59,149,088 (GRCm39) |
H261Q |
probably benign |
Het |
Or5m8 |
T |
C |
2: 85,822,376 (GRCm39) |
F72L |
probably benign |
Het |
Or9i1 |
T |
A |
19: 13,839,663 (GRCm39) |
C169S |
probably damaging |
Het |
Pgghg |
T |
C |
7: 140,525,633 (GRCm39) |
S479P |
|
Het |
Rnaseh2b |
T |
A |
14: 62,584,064 (GRCm39) |
F37I |
probably damaging |
Het |
Rtn4 |
T |
A |
11: 29,683,801 (GRCm39) |
I1031N |
probably damaging |
Het |
Rxfp2 |
A |
G |
5: 149,987,151 (GRCm39) |
E344G |
probably benign |
Het |
Scel |
A |
G |
14: 103,774,444 (GRCm39) |
R89G |
possibly damaging |
Het |
Sirt4 |
T |
C |
5: 115,621,055 (GRCm39) |
E39G |
probably benign |
Het |
Slc6a12 |
T |
A |
6: 121,331,334 (GRCm39) |
|
probably null |
Het |
Snapc3 |
C |
A |
4: 83,368,333 (GRCm39) |
H277N |
probably benign |
Het |
Susd2 |
A |
G |
10: 75,473,333 (GRCm39) |
|
probably null |
Het |
Tagap1 |
T |
C |
17: 7,223,826 (GRCm39) |
Q290R |
probably benign |
Het |
Tenm3 |
A |
T |
8: 48,732,233 (GRCm39) |
|
probably benign |
Het |
Tmem54 |
A |
T |
4: 129,002,073 (GRCm39) |
H40L |
probably damaging |
Het |
Tnks1bp1 |
T |
C |
2: 84,889,721 (GRCm39) |
S683P |
probably damaging |
Het |
Tnpo2 |
A |
G |
8: 85,777,131 (GRCm39) |
D547G |
probably benign |
Het |
Tpd52l2 |
G |
A |
2: 181,141,667 (GRCm39) |
V17M |
probably benign |
Het |
Trip11 |
T |
A |
12: 101,861,942 (GRCm39) |
T208S |
probably benign |
Het |
Ttc17 |
C |
A |
2: 94,194,721 (GRCm39) |
D551Y |
probably damaging |
Het |
Ttll12 |
A |
T |
15: 83,471,302 (GRCm39) |
W222R |
probably damaging |
Het |
Xkr8 |
A |
T |
4: 132,455,512 (GRCm39) |
I287N |
probably damaging |
Het |
Zdhhc2 |
G |
T |
8: 40,926,066 (GRCm39) |
G354C |
probably null |
Het |
Zfp13 |
C |
T |
17: 23,795,072 (GRCm39) |
A493T |
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 |
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 |
R7714:Otof
|
UTSW |
5 |
30,527,597 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|