Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
T |
A |
7: 119,950,036 (GRCm39) |
Y503* |
probably null |
Het |
Akap9 |
C |
A |
5: 4,026,235 (GRCm39) |
Q1297K |
possibly damaging |
Het |
Dffb |
T |
C |
4: 154,049,976 (GRCm39) |
T296A |
probably damaging |
Het |
Dpf1 |
G |
A |
7: 29,015,631 (GRCm39) |
|
probably null |
Het |
Elp1 |
A |
T |
4: 56,759,925 (GRCm39) |
|
probably null |
Het |
Grid2ip |
T |
C |
5: 143,371,774 (GRCm39) |
S666P |
probably damaging |
Het |
Gucy2e |
T |
A |
11: 69,115,877 (GRCm39) |
E835V |
probably damaging |
Het |
Hdac5 |
G |
A |
11: 102,086,644 (GRCm39) |
P120S |
probably benign |
Het |
Htr1d |
T |
C |
4: 136,170,815 (GRCm39) |
I348T |
probably damaging |
Het |
Hyal4 |
A |
T |
6: 24,765,737 (GRCm39) |
S364C |
probably damaging |
Het |
Igkv1-133 |
A |
T |
6: 67,701,944 (GRCm39) |
Q16L |
probably benign |
Het |
Itga10 |
C |
T |
3: 96,559,054 (GRCm39) |
|
probably benign |
Het |
Met |
A |
T |
6: 17,549,085 (GRCm39) |
D979V |
probably damaging |
Het |
Mga |
A |
G |
2: 119,772,245 (GRCm39) |
T1702A |
probably damaging |
Het |
Midn |
A |
G |
10: 79,986,144 (GRCm39) |
D78G |
probably benign |
Het |
Muc5b |
T |
C |
7: 141,405,595 (GRCm39) |
|
probably benign |
Het |
Or1e30 |
A |
G |
11: 73,678,567 (GRCm39) |
T268A |
probably benign |
Het |
Or5ak24 |
C |
T |
2: 85,260,837 (GRCm39) |
C112Y |
probably benign |
Het |
Or5b107 |
T |
A |
19: 13,143,020 (GRCm39) |
M214K |
probably benign |
Het |
Or8b48 |
A |
G |
9: 38,492,792 (GRCm39) |
Y73C |
probably damaging |
Het |
Pbld2 |
T |
C |
10: 62,897,470 (GRCm39) |
L57P |
probably damaging |
Het |
Phka2 |
T |
A |
X: 159,327,291 (GRCm39) |
Y334* |
probably null |
Het |
Plin4 |
G |
T |
17: 56,411,112 (GRCm39) |
T973K |
possibly damaging |
Het |
R3hdm4 |
C |
T |
10: 79,748,515 (GRCm39) |
R143H |
possibly damaging |
Het |
Rps18 |
G |
C |
17: 34,171,247 (GRCm39) |
|
probably null |
Het |
Samd9l |
A |
T |
6: 3,374,032 (GRCm39) |
C1076* |
probably null |
Het |
Scml4 |
T |
C |
10: 42,806,607 (GRCm39) |
|
probably benign |
Het |
Slc16a10 |
A |
G |
10: 40,017,890 (GRCm39) |
V48A |
probably benign |
Het |
Slc6a5 |
T |
C |
7: 49,567,371 (GRCm39) |
V275A |
probably benign |
Het |
Smad9 |
C |
T |
3: 54,696,705 (GRCm39) |
R257W |
probably damaging |
Het |
Snrpb |
C |
A |
2: 130,017,299 (GRCm39) |
R73L |
probably null |
Het |
Srsf9 |
C |
T |
5: 115,468,571 (GRCm39) |
A69V |
probably damaging |
Het |
Stfa2 |
A |
G |
16: 36,224,433 (GRCm39) |
Y90H |
probably damaging |
Het |
Tgm6 |
T |
A |
2: 129,993,681 (GRCm39) |
V640E |
possibly damaging |
Het |
Tnrc6c |
C |
T |
11: 117,640,451 (GRCm39) |
R1414C |
probably damaging |
Het |
Tyk2 |
A |
T |
9: 21,038,606 (GRCm39) |
C8S |
probably damaging |
Het |
Upp2 |
G |
A |
2: 58,680,128 (GRCm39) |
R300Q |
possibly damaging |
Het |
Utp20 |
A |
G |
10: 88,593,855 (GRCm39) |
|
probably benign |
Het |
Veph1 |
C |
T |
3: 66,122,858 (GRCm39) |
V224I |
probably benign |
Het |
Vmn1r30 |
A |
T |
6: 58,412,437 (GRCm39) |
F132I |
probably benign |
Het |
Vmn2r116 |
A |
G |
17: 23,605,025 (GRCm39) |
S113G |
probably benign |
Het |
Vps53 |
A |
C |
11: 76,008,609 (GRCm39) |
V237G |
probably benign |
Het |
|
Other mutations in Oma1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Oma1
|
APN |
4 |
103,176,565 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02317:Oma1
|
APN |
4 |
103,176,234 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02483:Oma1
|
APN |
4 |
103,182,309 (GRCm39) |
nonsense |
probably null |
|
R0032:Oma1
|
UTSW |
4 |
103,223,209 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0032:Oma1
|
UTSW |
4 |
103,223,209 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0386:Oma1
|
UTSW |
4 |
103,182,398 (GRCm39) |
splice site |
probably benign |
|
R0699:Oma1
|
UTSW |
4 |
103,210,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R0749:Oma1
|
UTSW |
4 |
103,182,496 (GRCm39) |
nonsense |
probably null |
|
R1809:Oma1
|
UTSW |
4 |
103,182,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R1990:Oma1
|
UTSW |
4 |
103,178,971 (GRCm39) |
missense |
probably damaging |
0.99 |
R4532:Oma1
|
UTSW |
4 |
103,176,571 (GRCm39) |
missense |
probably benign |
0.22 |
R4916:Oma1
|
UTSW |
4 |
103,176,727 (GRCm39) |
critical splice donor site |
probably null |
|
R8069:Oma1
|
UTSW |
4 |
103,176,232 (GRCm39) |
start gained |
probably benign |
|
R8290:Oma1
|
UTSW |
4 |
103,176,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R8411:Oma1
|
UTSW |
4 |
103,186,113 (GRCm39) |
nonsense |
probably null |
|
R8896:Oma1
|
UTSW |
4 |
103,210,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R9149:Oma1
|
UTSW |
4 |
103,182,214 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9605:Oma1
|
UTSW |
4 |
103,210,726 (GRCm39) |
missense |
possibly damaging |
0.91 |
|