Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 110,045,376 (GRCm39) |
F319S |
probably damaging |
Het |
Ap3b1 |
A |
G |
13: 94,664,827 (GRCm39) |
D922G |
unknown |
Het |
Bhlhe41 |
A |
T |
6: 145,809,882 (GRCm39) |
H107Q |
probably damaging |
Het |
Csmd2 |
C |
A |
4: 128,262,801 (GRCm39) |
H662Q |
probably benign |
Het |
Dnah8 |
T |
C |
17: 30,932,021 (GRCm39) |
V1463A |
probably benign |
Het |
Ebf3 |
A |
T |
7: 136,911,094 (GRCm39) |
V140E |
probably benign |
Het |
Havcr2 |
T |
A |
11: 46,370,108 (GRCm39) |
|
probably benign |
Het |
Hexb |
G |
A |
13: 97,313,401 (GRCm39) |
A485V |
probably damaging |
Het |
Igkv5-37 |
T |
A |
6: 69,940,473 (GRCm39) |
Q57L |
probably damaging |
Het |
Ipo5 |
T |
A |
14: 121,154,795 (GRCm39) |
S40T |
probably benign |
Het |
Kcnj8 |
A |
G |
6: 142,515,837 (GRCm39) |
M90T |
probably benign |
Het |
Kif21b |
T |
A |
1: 136,087,495 (GRCm39) |
L937Q |
probably damaging |
Het |
Kmt2c |
A |
C |
5: 25,515,155 (GRCm39) |
L2896R |
probably damaging |
Het |
Ldlrap1 |
A |
T |
4: 134,484,706 (GRCm39) |
I96N |
probably damaging |
Het |
Leo1 |
A |
G |
9: 75,353,281 (GRCm39) |
|
probably benign |
Het |
Mbnl2 |
T |
C |
14: 120,642,059 (GRCm39) |
M341T |
probably benign |
Het |
Nfatc2 |
G |
A |
2: 168,348,821 (GRCm39) |
R669* |
probably null |
Het |
Nhlrc2 |
T |
A |
19: 56,563,280 (GRCm39) |
V293E |
probably damaging |
Het |
Or1e17 |
T |
C |
11: 73,831,276 (GRCm39) |
F68S |
possibly damaging |
Het |
Or2at1 |
A |
G |
7: 99,417,179 (GRCm39) |
D270G |
possibly damaging |
Het |
Or51ag1 |
A |
T |
7: 103,155,295 (GRCm39) |
M286K |
probably benign |
Het |
Or51ai2 |
A |
G |
7: 103,586,770 (GRCm39) |
Q61R |
possibly damaging |
Het |
Pcnt |
T |
C |
10: 76,278,393 (GRCm39) |
|
probably benign |
Het |
Recql4 |
G |
T |
15: 76,592,771 (GRCm39) |
Q307K |
possibly damaging |
Het |
Sp140 |
T |
A |
1: 85,570,730 (GRCm39) |
Y453* |
probably null |
Het |
Sspo |
G |
A |
6: 48,461,639 (GRCm39) |
V3600I |
possibly damaging |
Het |
Sybu |
T |
C |
15: 44,536,619 (GRCm39) |
E441G |
probably benign |
Het |
Syne3 |
A |
T |
12: 104,929,553 (GRCm39) |
H222Q |
probably damaging |
Het |
Tef |
T |
C |
15: 81,705,496 (GRCm39) |
V173A |
probably benign |
Het |
Tlcd1 |
A |
G |
11: 78,071,160 (GRCm39) |
|
probably null |
Het |
Tmod4 |
C |
A |
3: 95,032,953 (GRCm39) |
Q30K |
probably benign |
Het |
Tpgs1 |
T |
C |
10: 79,511,322 (GRCm39) |
Y155H |
probably damaging |
Het |
Trib3 |
G |
A |
2: 152,185,070 (GRCm39) |
P60S |
probably benign |
Het |
Ttn |
T |
A |
2: 76,560,550 (GRCm39) |
T20957S |
probably damaging |
Het |
Vars1 |
T |
C |
17: 35,234,460 (GRCm39) |
|
probably benign |
Het |
Vps13c |
T |
C |
9: 67,852,763 (GRCm39) |
|
probably benign |
Het |
Zc3h4 |
T |
C |
7: 16,168,002 (GRCm39) |
S704P |
unknown |
Het |
Zfp644 |
G |
A |
5: 106,785,180 (GRCm39) |
R456W |
probably damaging |
Het |
|
Other mutations in Otoa |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01469:Otoa
|
APN |
7 |
120,754,496 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01791:Otoa
|
APN |
7 |
120,755,072 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01924:Otoa
|
APN |
7 |
120,705,191 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01953:Otoa
|
APN |
7 |
120,759,548 (GRCm39) |
splice site |
probably null |
|
IGL02121:Otoa
|
APN |
7 |
120,721,247 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02390:Otoa
|
APN |
7 |
120,730,590 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02591:Otoa
|
APN |
7 |
120,755,053 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02811:Otoa
|
APN |
7 |
120,717,878 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02878:Otoa
|
APN |
7 |
120,743,076 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03328:Otoa
|
APN |
7 |
120,710,217 (GRCm39) |
missense |
probably damaging |
0.98 |
R0056:Otoa
|
UTSW |
7 |
120,730,570 (GRCm39) |
missense |
probably benign |
0.00 |
R0279:Otoa
|
UTSW |
7 |
120,710,302 (GRCm39) |
splice site |
probably benign |
|
R0390:Otoa
|
UTSW |
7 |
120,730,564 (GRCm39) |
missense |
probably benign |
0.07 |
R0411:Otoa
|
UTSW |
7 |
120,755,750 (GRCm39) |
critical splice donor site |
probably null |
|
R0628:Otoa
|
UTSW |
7 |
120,744,873 (GRCm39) |
splice site |
probably benign |
|
R1113:Otoa
|
UTSW |
7 |
120,724,666 (GRCm39) |
nonsense |
probably null |
|
R1240:Otoa
|
UTSW |
7 |
120,755,713 (GRCm39) |
missense |
probably benign |
|
R1308:Otoa
|
UTSW |
7 |
120,724,666 (GRCm39) |
nonsense |
probably null |
|
R1692:Otoa
|
UTSW |
7 |
120,690,774 (GRCm39) |
missense |
probably damaging |
0.99 |
R1728:Otoa
|
UTSW |
7 |
120,724,662 (GRCm39) |
missense |
probably benign |
0.36 |
R1729:Otoa
|
UTSW |
7 |
120,724,662 (GRCm39) |
missense |
probably benign |
0.36 |
R1744:Otoa
|
UTSW |
7 |
120,726,999 (GRCm39) |
splice site |
probably benign |
|
R1759:Otoa
|
UTSW |
7 |
120,733,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Otoa
|
UTSW |
7 |
120,724,662 (GRCm39) |
missense |
probably benign |
0.36 |
R1817:Otoa
|
UTSW |
7 |
120,759,753 (GRCm39) |
utr 3 prime |
probably benign |
|
R1961:Otoa
|
UTSW |
7 |
120,717,792 (GRCm39) |
missense |
probably benign |
0.05 |
R2061:Otoa
|
UTSW |
7 |
120,730,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R2509:Otoa
|
UTSW |
7 |
120,759,695 (GRCm39) |
missense |
probably benign |
|
R2510:Otoa
|
UTSW |
7 |
120,759,695 (GRCm39) |
missense |
probably benign |
|
R3411:Otoa
|
UTSW |
7 |
120,721,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R3438:Otoa
|
UTSW |
7 |
120,759,566 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3905:Otoa
|
UTSW |
7 |
120,724,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R3907:Otoa
|
UTSW |
7 |
120,724,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Otoa
|
UTSW |
7 |
120,744,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R4751:Otoa
|
UTSW |
7 |
120,732,147 (GRCm39) |
critical splice donor site |
probably benign |
|
R4896:Otoa
|
UTSW |
7 |
120,701,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R4932:Otoa
|
UTSW |
7 |
120,754,358 (GRCm39) |
missense |
probably damaging |
0.98 |
R5224:Otoa
|
UTSW |
7 |
120,739,016 (GRCm39) |
missense |
probably damaging |
0.98 |
R5235:Otoa
|
UTSW |
7 |
120,755,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R5595:Otoa
|
UTSW |
7 |
120,721,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R5891:Otoa
|
UTSW |
7 |
120,731,583 (GRCm39) |
splice site |
probably null |
|
R5894:Otoa
|
UTSW |
7 |
120,721,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Otoa
|
UTSW |
7 |
120,693,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R5976:Otoa
|
UTSW |
7 |
120,726,936 (GRCm39) |
missense |
probably benign |
0.00 |
R6464:Otoa
|
UTSW |
7 |
120,701,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R6761:Otoa
|
UTSW |
7 |
120,721,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R6770:Otoa
|
UTSW |
7 |
120,744,837 (GRCm39) |
missense |
probably benign |
0.25 |
R6821:Otoa
|
UTSW |
7 |
120,692,070 (GRCm39) |
critical splice donor site |
probably null |
|
R6924:Otoa
|
UTSW |
7 |
120,730,724 (GRCm39) |
splice site |
probably null |
|
R7016:Otoa
|
UTSW |
7 |
120,746,989 (GRCm39) |
missense |
probably damaging |
0.99 |
R7215:Otoa
|
UTSW |
7 |
120,717,795 (GRCm39) |
missense |
unknown |
|
R7313:Otoa
|
UTSW |
7 |
120,701,765 (GRCm39) |
missense |
probably benign |
0.42 |
R7340:Otoa
|
UTSW |
7 |
120,729,288 (GRCm39) |
missense |
probably benign |
0.38 |
R7443:Otoa
|
UTSW |
7 |
120,731,633 (GRCm39) |
missense |
probably benign |
0.00 |
R7559:Otoa
|
UTSW |
7 |
120,743,149 (GRCm39) |
missense |
probably damaging |
0.99 |
R7640:Otoa
|
UTSW |
7 |
120,744,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R7654:Otoa
|
UTSW |
7 |
120,746,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R7659:Otoa
|
UTSW |
7 |
120,733,267 (GRCm39) |
missense |
probably benign |
0.01 |
R8421:Otoa
|
UTSW |
7 |
120,698,491 (GRCm39) |
critical splice donor site |
probably null |
|
R8799:Otoa
|
UTSW |
7 |
120,691,894 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8954:Otoa
|
UTSW |
7 |
120,744,741 (GRCm39) |
nonsense |
probably null |
|
R9099:Otoa
|
UTSW |
7 |
120,739,055 (GRCm39) |
missense |
probably benign |
|
R9126:Otoa
|
UTSW |
7 |
120,693,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R9369:Otoa
|
UTSW |
7 |
120,744,840 (GRCm39) |
missense |
probably benign |
0.23 |
U24488:Otoa
|
UTSW |
7 |
120,717,763 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0023:Otoa
|
UTSW |
7 |
120,717,794 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Otoa
|
UTSW |
7 |
120,717,878 (GRCm39) |
missense |
probably benign |
0.00 |
|