Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930022D16Rik |
T |
C |
11: 109,308,737 (GRCm39) |
|
probably benign |
Het |
Aatk |
T |
C |
11: 119,903,101 (GRCm39) |
S375G |
probably benign |
Het |
Abcg8 |
T |
C |
17: 84,999,423 (GRCm39) |
M173T |
probably benign |
Het |
B3galt2 |
A |
C |
1: 143,522,495 (GRCm39) |
R210S |
probably benign |
Het |
Bltp1 |
G |
T |
3: 37,061,133 (GRCm39) |
|
probably null |
Het |
Capn5 |
C |
T |
7: 97,784,971 (GRCm39) |
A168T |
probably damaging |
Het |
Cbx7 |
C |
T |
15: 79,814,829 (GRCm39) |
G24D |
probably damaging |
Het |
Ccdc7a |
A |
T |
8: 129,788,099 (GRCm39) |
S77T |
probably benign |
Het |
Cd200r2 |
T |
A |
16: 44,729,832 (GRCm39) |
|
probably benign |
Het |
Cdh11 |
T |
C |
8: 103,406,377 (GRCm39) |
H32R |
probably benign |
Het |
Chdh |
A |
T |
14: 29,753,289 (GRCm39) |
N66I |
probably benign |
Het |
Clca3a2 |
G |
A |
3: 144,519,388 (GRCm39) |
Q263* |
probably null |
Het |
Dcc |
T |
C |
18: 71,942,161 (GRCm39) |
I319V |
probably benign |
Het |
Depdc5 |
G |
T |
5: 33,050,745 (GRCm39) |
M170I |
probably damaging |
Het |
Dop1b |
T |
A |
16: 93,607,117 (GRCm39) |
L2140Q |
probably benign |
Het |
Frem3 |
G |
A |
8: 81,341,763 (GRCm39) |
G1352E |
probably benign |
Het |
Fsd1l |
T |
A |
4: 53,694,742 (GRCm39) |
C389S |
probably damaging |
Het |
Grin2c |
C |
T |
11: 115,148,936 (GRCm39) |
A221T |
possibly damaging |
Het |
Gstz1 |
C |
A |
12: 87,210,575 (GRCm39) |
P153T |
probably damaging |
Het |
Itgb2 |
T |
C |
10: 77,378,237 (GRCm39) |
S22P |
possibly damaging |
Het |
Krt87 |
G |
T |
15: 101,336,312 (GRCm39) |
Q114K |
possibly damaging |
Het |
Krtap5-4 |
A |
C |
7: 141,857,647 (GRCm39) |
S106R |
unknown |
Het |
Lats1 |
T |
C |
10: 7,581,435 (GRCm39) |
V740A |
probably damaging |
Het |
Mcm9 |
C |
A |
10: 53,506,041 (GRCm39) |
G78C |
probably damaging |
Het |
Mn1 |
G |
A |
5: 111,569,413 (GRCm39) |
E1128K |
possibly damaging |
Het |
Myo1f |
G |
A |
17: 33,811,977 (GRCm39) |
R592H |
possibly damaging |
Het |
Nfat5 |
G |
T |
8: 108,094,146 (GRCm39) |
A277S |
probably damaging |
Het |
Nfkbia |
T |
A |
12: 55,537,327 (GRCm39) |
Y254F |
probably damaging |
Het |
Nr3c2 |
A |
T |
8: 77,635,843 (GRCm39) |
N315Y |
probably damaging |
Het |
Panx3 |
C |
T |
9: 37,572,767 (GRCm39) |
C261Y |
probably damaging |
Het |
Pdia2 |
C |
A |
17: 26,417,896 (GRCm39) |
G38W |
probably damaging |
Het |
Psg19 |
G |
T |
7: 18,527,971 (GRCm39) |
Y257* |
probably null |
Het |
Ptpre |
A |
T |
7: 135,280,054 (GRCm39) |
K586* |
probably null |
Het |
Reps1 |
A |
G |
10: 18,000,643 (GRCm39) |
R752G |
probably damaging |
Het |
Rpgrip1 |
T |
A |
14: 52,368,633 (GRCm39) |
D277E |
possibly damaging |
Het |
Rpl21-ps6 |
A |
G |
17: 56,222,671 (GRCm39) |
|
noncoding transcript |
Het |
Serpinf2 |
T |
A |
11: 75,327,333 (GRCm39) |
E198V |
possibly damaging |
Het |
Sh3tc1 |
A |
G |
5: 35,860,719 (GRCm39) |
L1046P |
probably damaging |
Het |
Snw1 |
T |
C |
12: 87,497,711 (GRCm39) |
E426G |
probably benign |
Het |
Sord |
T |
A |
2: 122,094,564 (GRCm39) |
N317K |
probably benign |
Het |
Taar3 |
A |
T |
10: 23,826,330 (GRCm39) |
D292V |
probably damaging |
Het |
Tdrd3 |
C |
A |
14: 87,709,618 (GRCm39) |
T94K |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,687,165 (GRCm39) |
E736* |
probably null |
Het |
Usp32 |
A |
G |
11: 84,930,091 (GRCm39) |
V562A |
probably damaging |
Het |
Vmn1r169 |
T |
G |
7: 23,276,611 (GRCm39) |
M1R |
probably null |
Het |
Vmn2r3 |
C |
T |
3: 64,167,304 (GRCm39) |
C609Y |
probably damaging |
Het |
Vmn2r69 |
T |
C |
7: 85,055,739 (GRCm39) |
T800A |
probably benign |
Het |
Vmn2r72 |
G |
A |
7: 85,387,542 (GRCm39) |
T674I |
probably benign |
Het |
Zfp160 |
T |
A |
17: 21,241,088 (GRCm39) |
M52K |
possibly damaging |
Het |
Zfp607a |
T |
A |
7: 27,578,042 (GRCm39) |
C371S |
probably damaging |
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 |
|
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 |
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 |
|