Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900092C05Rik |
T |
C |
7: 12,284,459 (GRCm39) |
I102T |
possibly damaging |
Het |
4933412E24Rik |
C |
A |
15: 59,887,424 (GRCm39) |
A339S |
possibly damaging |
Het |
Ackr2 |
A |
G |
9: 121,738,185 (GRCm39) |
T187A |
probably benign |
Het |
Adam28 |
A |
G |
14: 68,844,956 (GRCm39) |
V777A |
probably benign |
Het |
Add3 |
T |
A |
19: 53,227,861 (GRCm39) |
D515E |
probably damaging |
Het |
Aire |
C |
A |
10: 77,872,557 (GRCm39) |
E354* |
probably null |
Het |
AW551984 |
T |
C |
9: 39,502,568 (GRCm39) |
K670R |
probably benign |
Het |
Bahcc1 |
T |
C |
11: 120,162,563 (GRCm39) |
V287A |
probably benign |
Het |
Brca1 |
T |
C |
11: 101,415,002 (GRCm39) |
N1044S |
possibly damaging |
Het |
Bub1b |
T |
A |
2: 118,467,230 (GRCm39) |
I851N |
probably damaging |
Het |
Ceacam11 |
A |
T |
7: 17,707,323 (GRCm39) |
I36F |
possibly damaging |
Het |
Copa |
A |
G |
1: 171,940,756 (GRCm39) |
E714G |
probably benign |
Het |
Cth |
A |
T |
3: 157,630,572 (GRCm39) |
N32K |
probably benign |
Het |
Cyp2a5 |
T |
A |
7: 26,540,434 (GRCm39) |
M349K |
probably damaging |
Het |
D130052B06Rik |
A |
G |
11: 33,573,966 (GRCm39) |
S188G |
unknown |
Het |
Fhdc1 |
G |
A |
3: 84,352,042 (GRCm39) |
A1061V |
possibly damaging |
Het |
Flt1 |
T |
C |
5: 147,508,271 (GRCm39) |
N1161S |
probably benign |
Het |
Hip1 |
T |
C |
5: 135,573,917 (GRCm39) |
|
probably benign |
Het |
Mapk11 |
A |
G |
15: 89,031,046 (GRCm39) |
|
probably benign |
Het |
Mtif2 |
A |
G |
11: 29,494,417 (GRCm39) |
|
probably benign |
Het |
Nipsnap1 |
G |
A |
11: 4,839,912 (GRCm39) |
R211H |
probably damaging |
Het |
Or52ab4 |
A |
G |
7: 102,987,435 (GRCm39) |
H58R |
probably damaging |
Het |
Or6c35 |
T |
C |
10: 129,169,326 (GRCm39) |
I192T |
probably benign |
Het |
Pcdh1 |
A |
T |
18: 38,336,302 (GRCm39) |
I111N |
probably damaging |
Het |
Piezo2 |
T |
A |
18: 63,175,859 (GRCm39) |
I1841F |
probably damaging |
Het |
Pirb |
G |
T |
7: 3,720,175 (GRCm39) |
Y399* |
probably null |
Het |
Ppp1r36 |
A |
T |
12: 76,486,006 (GRCm39) |
N388I |
possibly damaging |
Het |
Prr16 |
A |
G |
18: 51,436,061 (GRCm39) |
D180G |
possibly damaging |
Het |
Prss39 |
A |
G |
1: 34,541,280 (GRCm39) |
|
probably null |
Het |
Spopfm2 |
T |
A |
3: 94,083,544 (GRCm39) |
K89M |
probably damaging |
Het |
Trank1 |
T |
A |
9: 111,178,431 (GRCm39) |
V373D |
probably damaging |
Het |
Ubn1 |
A |
G |
16: 4,889,923 (GRCm39) |
E186G |
probably damaging |
Het |
Zmym2 |
T |
C |
14: 57,184,029 (GRCm39) |
V997A |
probably benign |
Het |
|
Other mutations in Myo1f |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00851:Myo1f
|
APN |
17 |
33,800,938 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01019:Myo1f
|
APN |
17 |
33,811,977 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01524:Myo1f
|
APN |
17 |
33,798,857 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01951:Myo1f
|
APN |
17 |
33,816,991 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02132:Myo1f
|
APN |
17 |
33,798,945 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02170:Myo1f
|
APN |
17 |
33,797,246 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02173:Myo1f
|
APN |
17 |
33,826,318 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02277:Myo1f
|
APN |
17 |
33,798,835 (GRCm39) |
splice site |
probably null |
|
IGL02550:Myo1f
|
APN |
17 |
33,799,124 (GRCm39) |
unclassified |
probably benign |
|
IGL02550:Myo1f
|
APN |
17 |
33,807,116 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02615:Myo1f
|
APN |
17 |
33,823,630 (GRCm39) |
missense |
probably benign |
|
IGL02801:Myo1f
|
APN |
17 |
33,797,111 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02817:Myo1f
|
APN |
17 |
33,823,532 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02904:Myo1f
|
APN |
17 |
33,804,632 (GRCm39) |
nonsense |
probably null |
|
IGL03056:Myo1f
|
APN |
17 |
33,804,574 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03334:Myo1f
|
APN |
17 |
33,817,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Myo1f
|
UTSW |
17 |
33,820,677 (GRCm39) |
missense |
probably damaging |
0.98 |
R0066:Myo1f
|
UTSW |
17 |
33,820,677 (GRCm39) |
missense |
probably damaging |
0.98 |
R0321:Myo1f
|
UTSW |
17 |
33,811,986 (GRCm39) |
missense |
probably benign |
0.31 |
R0375:Myo1f
|
UTSW |
17 |
33,820,930 (GRCm39) |
missense |
probably benign |
0.27 |
R0487:Myo1f
|
UTSW |
17 |
33,797,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R0925:Myo1f
|
UTSW |
17 |
33,797,107 (GRCm39) |
missense |
probably damaging |
0.96 |
R1394:Myo1f
|
UTSW |
17 |
33,802,714 (GRCm39) |
missense |
probably damaging |
0.96 |
R1395:Myo1f
|
UTSW |
17 |
33,802,714 (GRCm39) |
missense |
probably damaging |
0.96 |
R1474:Myo1f
|
UTSW |
17 |
33,813,001 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1760:Myo1f
|
UTSW |
17 |
33,805,172 (GRCm39) |
missense |
probably benign |
0.03 |
R1965:Myo1f
|
UTSW |
17 |
33,817,146 (GRCm39) |
nonsense |
probably null |
|
R2409:Myo1f
|
UTSW |
17 |
33,795,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R2432:Myo1f
|
UTSW |
17 |
33,794,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Myo1f
|
UTSW |
17 |
33,801,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Myo1f
|
UTSW |
17 |
33,817,165 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5239:Myo1f
|
UTSW |
17 |
33,820,709 (GRCm39) |
missense |
probably benign |
0.00 |
R5881:Myo1f
|
UTSW |
17 |
33,799,259 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5881:Myo1f
|
UTSW |
17 |
33,795,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R6160:Myo1f
|
UTSW |
17 |
33,823,318 (GRCm39) |
missense |
probably benign |
|
R6210:Myo1f
|
UTSW |
17 |
33,820,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R6365:Myo1f
|
UTSW |
17 |
33,805,090 (GRCm39) |
missense |
probably benign |
|
R6464:Myo1f
|
UTSW |
17 |
33,795,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R6532:Myo1f
|
UTSW |
17 |
33,794,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R6678:Myo1f
|
UTSW |
17 |
33,794,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R7241:Myo1f
|
UTSW |
17 |
33,798,902 (GRCm39) |
missense |
probably damaging |
0.99 |
R7266:Myo1f
|
UTSW |
17 |
33,820,668 (GRCm39) |
missense |
probably benign |
|
R7513:Myo1f
|
UTSW |
17 |
33,794,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R7606:Myo1f
|
UTSW |
17 |
33,795,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R7779:Myo1f
|
UTSW |
17 |
33,797,247 (GRCm39) |
missense |
probably benign |
0.27 |
R7853:Myo1f
|
UTSW |
17 |
33,795,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7884:Myo1f
|
UTSW |
17 |
33,817,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Myo1f
|
UTSW |
17 |
33,816,992 (GRCm39) |
missense |
probably benign |
0.09 |
R8807:Myo1f
|
UTSW |
17 |
33,794,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R9009:Myo1f
|
UTSW |
17 |
33,823,662 (GRCm39) |
missense |
probably benign |
0.12 |
R9083:Myo1f
|
UTSW |
17 |
33,813,036 (GRCm39) |
missense |
probably damaging |
0.99 |
R9227:Myo1f
|
UTSW |
17 |
33,795,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R9230:Myo1f
|
UTSW |
17 |
33,795,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R9528:Myo1f
|
UTSW |
17 |
33,797,156 (GRCm39) |
critical splice donor site |
probably null |
|
X0028:Myo1f
|
UTSW |
17 |
33,795,412 (GRCm39) |
missense |
possibly damaging |
0.67 |
X0065:Myo1f
|
UTSW |
17 |
33,820,957 (GRCm39) |
missense |
probably benign |
|
|