Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700028K03Rik |
A |
G |
5: 107,687,057 (GRCm39) |
T15A |
possibly damaging |
Het |
2010315B03Rik |
G |
T |
9: 124,056,652 (GRCm39) |
Q91K |
|
Het |
2210408I21Rik |
A |
G |
13: 77,407,988 (GRCm39) |
N419S |
possibly damaging |
Het |
Abhd2 |
A |
G |
7: 78,998,020 (GRCm39) |
E184G |
probably damaging |
Het |
Adgrg3 |
T |
C |
8: 95,766,186 (GRCm39) |
I339T |
probably benign |
Het |
Adgrv1 |
C |
T |
13: 81,567,178 (GRCm39) |
A5332T |
|
Het |
Akap13 |
T |
C |
7: 75,293,193 (GRCm39) |
V42A |
|
Het |
Akap6 |
A |
G |
12: 52,842,672 (GRCm39) |
T7A |
probably benign |
Het |
Apob |
A |
T |
12: 8,052,069 (GRCm39) |
D1170V |
probably damaging |
Het |
Atad1 |
A |
G |
19: 32,684,323 (GRCm39) |
I25T |
possibly damaging |
Het |
Atp4b |
G |
T |
8: 13,436,746 (GRCm39) |
N255K |
probably damaging |
Het |
Atr |
C |
T |
9: 95,792,610 (GRCm39) |
A1644V |
possibly damaging |
Het |
Bpnt1 |
T |
A |
1: 185,077,584 (GRCm39) |
C100S |
probably damaging |
Het |
C1rl |
C |
T |
6: 124,484,054 (GRCm39) |
L203F |
probably benign |
Het |
Clasp2 |
T |
A |
9: 113,705,372 (GRCm39) |
V576D |
probably damaging |
Het |
Col8a2 |
A |
G |
4: 126,205,273 (GRCm39) |
T428A |
unknown |
Het |
Copg2 |
T |
A |
6: 30,749,505 (GRCm39) |
|
probably null |
Het |
Cpn2 |
C |
T |
16: 30,078,759 (GRCm39) |
R314H |
possibly damaging |
Het |
Cpt2 |
G |
A |
4: 107,764,354 (GRCm39) |
A470V |
probably damaging |
Het |
Cyp2a4 |
C |
T |
7: 26,011,688 (GRCm39) |
T303I |
probably damaging |
Het |
Ddx42 |
A |
G |
11: 106,132,606 (GRCm39) |
D543G |
probably benign |
Het |
Dip2a |
T |
C |
10: 76,112,438 (GRCm39) |
T1087A |
probably damaging |
Het |
Fam219b |
T |
C |
9: 57,444,919 (GRCm39) |
F6L |
probably benign |
Het |
Fsip2 |
G |
T |
2: 82,807,972 (GRCm39) |
L1430F |
probably damaging |
Het |
Fstl4 |
A |
G |
11: 53,075,466 (GRCm39) |
I573V |
probably benign |
Het |
Ggnbp2 |
A |
T |
11: 84,745,188 (GRCm39) |
S182R |
probably benign |
Het |
Glud1 |
A |
G |
14: 34,061,931 (GRCm39) |
T484A |
probably benign |
Het |
Gm19410 |
A |
G |
8: 36,257,608 (GRCm39) |
N682S |
probably benign |
Het |
Gnao1 |
T |
C |
8: 94,622,861 (GRCm39) |
I55T |
|
Het |
H2bc15 |
G |
T |
13: 21,938,305 (GRCm39) |
A5S |
unknown |
Het |
Hcn4 |
C |
T |
9: 58,766,809 (GRCm39) |
S790L |
unknown |
Het |
Ighv3-4 |
T |
C |
12: 114,217,393 (GRCm39) |
E66G |
probably damaging |
Het |
Igkv6-23 |
A |
G |
6: 70,237,526 (GRCm39) |
S72P |
probably damaging |
Het |
Kdm7a |
A |
C |
6: 39,147,767 (GRCm39) |
Y213D |
probably damaging |
Het |
Klk15 |
T |
G |
7: 43,587,770 (GRCm39) |
M66R |
possibly damaging |
Het |
Lce1d |
T |
A |
3: 92,593,363 (GRCm39) |
T17S |
unknown |
Het |
Lipt1 |
T |
C |
1: 37,914,534 (GRCm39) |
Y197H |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 41,660,978 (GRCm39) |
D157E |
|
Het |
Ltbp1 |
A |
G |
17: 75,697,498 (GRCm39) |
T1697A |
probably benign |
Het |
Marchf6 |
T |
C |
15: 31,498,845 (GRCm39) |
T151A |
probably benign |
Het |
Muc5b |
G |
A |
7: 141,396,116 (GRCm39) |
R124H |
unknown |
Het |
Myo5b |
A |
G |
18: 74,861,968 (GRCm39) |
N1320S |
possibly damaging |
Het |
Myt1l |
T |
A |
12: 29,877,611 (GRCm39) |
S421T |
unknown |
Het |
Nav1 |
A |
T |
1: 135,379,929 (GRCm39) |
M1531K |
unknown |
Het |
Nlrp4e |
A |
G |
7: 23,054,636 (GRCm39) |
D930G |
probably benign |
Het |
Nup210l |
C |
T |
3: 90,107,173 (GRCm39) |
P1570L |
probably benign |
Het |
Or51a6 |
A |
G |
7: 102,604,464 (GRCm39) |
S115P |
probably damaging |
Het |
Or5b112 |
G |
T |
19: 13,319,848 (GRCm39) |
C242F |
probably damaging |
Het |
Or5d47 |
A |
T |
2: 87,804,945 (GRCm39) |
Y21* |
probably null |
Het |
Or6k14 |
A |
T |
1: 173,927,608 (GRCm39) |
I195F |
probably damaging |
Het |
Or7g30 |
G |
A |
9: 19,352,580 (GRCm39) |
V124I |
possibly damaging |
Het |
Oxct2b |
A |
T |
4: 123,011,483 (GRCm39) |
I468F |
probably damaging |
Het |
Pcdhgb7 |
T |
A |
18: 37,886,636 (GRCm39) |
L602Q |
probably damaging |
Het |
Prrc2c |
A |
G |
1: 162,525,298 (GRCm39) |
V1862A |
unknown |
Het |
Rad54l2 |
C |
T |
9: 106,573,151 (GRCm39) |
R1110H |
probably damaging |
Het |
Rere |
T |
A |
4: 150,703,636 (GRCm39) |
H180Q |
probably damaging |
Het |
Rtl1 |
C |
T |
12: 109,561,113 (GRCm39) |
R242Q |
unknown |
Het |
Sfxn4 |
T |
C |
19: 60,845,807 (GRCm39) |
D63G |
probably damaging |
Het |
Strn |
C |
T |
17: 78,967,575 (GRCm39) |
A579T |
probably benign |
Het |
Stxbp3 |
A |
G |
3: 108,747,756 (GRCm39) |
L10P |
probably damaging |
Het |
Swi5 |
T |
C |
2: 32,170,739 (GRCm39) |
M95V |
possibly damaging |
Het |
Tln2 |
T |
C |
9: 67,165,766 (GRCm39) |
Y1027C |
probably damaging |
Het |
Tmem65 |
A |
G |
15: 58,662,002 (GRCm39) |
|
probably null |
Het |
Tox4 |
C |
T |
14: 52,529,166 (GRCm39) |
P376S |
probably benign |
Het |
Tsg101 |
C |
T |
7: 46,542,308 (GRCm39) |
G215D |
possibly damaging |
Het |
Utp18 |
A |
G |
11: 93,768,833 (GRCm39) |
S226P |
probably damaging |
Het |
Vipr2 |
T |
C |
12: 116,093,788 (GRCm39) |
S174P |
probably damaging |
Het |
Vmn2r24 |
G |
T |
6: 123,763,950 (GRCm39) |
V276F |
possibly damaging |
Het |
Wdr26 |
T |
C |
1: 181,013,620 (GRCm39) |
R418G |
probably benign |
Het |
Zfp235 |
T |
C |
7: 23,840,381 (GRCm39) |
Y267H |
probably benign |
Het |
|
Other mutations in Or5b120 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01926:Or5b120
|
APN |
19 |
13,480,105 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02394:Or5b120
|
APN |
19 |
13,480,228 (GRCm39) |
missense |
probably damaging |
0.97 |
R0047:Or5b120
|
UTSW |
19 |
13,479,953 (GRCm39) |
missense |
probably benign |
0.30 |
R0047:Or5b120
|
UTSW |
19 |
13,479,953 (GRCm39) |
missense |
probably benign |
0.30 |
R0356:Or5b120
|
UTSW |
19 |
13,480,441 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0617:Or5b120
|
UTSW |
19 |
13,479,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R1589:Or5b120
|
UTSW |
19 |
13,480,121 (GRCm39) |
missense |
probably benign |
0.03 |
R1725:Or5b120
|
UTSW |
19 |
13,479,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Or5b120
|
UTSW |
19 |
13,479,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R2362:Or5b120
|
UTSW |
19 |
13,479,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R3402:Or5b120
|
UTSW |
19 |
13,480,312 (GRCm39) |
missense |
probably benign |
0.11 |
R4513:Or5b120
|
UTSW |
19 |
13,479,986 (GRCm39) |
missense |
probably benign |
0.05 |
R5197:Or5b120
|
UTSW |
19 |
13,479,748 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5205:Or5b120
|
UTSW |
19 |
13,480,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R5511:Or5b120
|
UTSW |
19 |
13,480,556 (GRCm39) |
missense |
probably benign |
0.12 |
R5838:Or5b120
|
UTSW |
19 |
13,479,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R6023:Or5b120
|
UTSW |
19 |
13,480,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R6232:Or5b120
|
UTSW |
19 |
13,480,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R6700:Or5b120
|
UTSW |
19 |
13,480,177 (GRCm39) |
missense |
probably damaging |
0.97 |
R6769:Or5b120
|
UTSW |
19 |
13,480,318 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6771:Or5b120
|
UTSW |
19 |
13,480,318 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7002:Or5b120
|
UTSW |
19 |
13,480,039 (GRCm39) |
missense |
probably benign |
0.00 |
R7057:Or5b120
|
UTSW |
19 |
13,480,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Or5b120
|
UTSW |
19 |
13,480,544 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7827:Or5b120
|
UTSW |
19 |
13,480,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R7913:Or5b120
|
UTSW |
19 |
13,480,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R9199:Or5b120
|
UTSW |
19 |
13,480,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R9286:Or5b120
|
UTSW |
19 |
13,479,791 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9606:Or5b120
|
UTSW |
19 |
13,479,943 (GRCm39) |
nonsense |
probably null |
|
|