Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
C |
A |
1: 130,670,584 (GRCm39) |
Q269K |
probably benign |
Het |
Acad9 |
T |
A |
3: 36,128,547 (GRCm39) |
I136N |
possibly damaging |
Het |
Adtrp |
A |
G |
13: 41,931,039 (GRCm39) |
S183P |
probably damaging |
Het |
Atp11b |
C |
T |
3: 35,887,086 (GRCm39) |
T690I |
probably damaging |
Het |
Bcl2l12 |
G |
A |
7: 44,640,818 (GRCm39) |
|
probably benign |
Het |
Btnl7-ps |
T |
A |
17: 34,752,503 (GRCm39) |
|
noncoding transcript |
Het |
Ccl12 |
T |
C |
11: 81,993,460 (GRCm39) |
C33R |
probably damaging |
Het |
Cdc25a |
T |
A |
9: 109,706,229 (GRCm39) |
S57R |
probably benign |
Het |
Coro2a |
T |
A |
4: 46,542,372 (GRCm39) |
|
probably benign |
Het |
Cpne6 |
T |
C |
14: 55,749,605 (GRCm39) |
V55A |
possibly damaging |
Het |
Ddn |
A |
G |
15: 98,704,207 (GRCm39) |
S362P |
possibly damaging |
Het |
Dmpk |
C |
G |
7: 18,821,944 (GRCm39) |
L301V |
probably benign |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Donson |
A |
G |
16: 91,478,181 (GRCm39) |
V258A |
possibly damaging |
Het |
Gm3336 |
G |
A |
8: 71,174,524 (GRCm39) |
V163I |
probably benign |
Het |
Gper1 |
C |
T |
5: 139,412,413 (GRCm39) |
R253C |
probably damaging |
Het |
Gpsm1 |
T |
A |
2: 26,217,476 (GRCm39) |
|
probably benign |
Het |
Hip1 |
A |
G |
5: 135,469,156 (GRCm39) |
S251P |
probably damaging |
Het |
Ifi214 |
A |
G |
1: 173,354,200 (GRCm39) |
S157P |
possibly damaging |
Het |
Igkv4-80 |
A |
C |
6: 68,993,649 (GRCm39) |
S81A |
probably benign |
Het |
Kntc1 |
T |
C |
5: 123,937,907 (GRCm39) |
V1535A |
probably benign |
Het |
Mbd3l1 |
A |
G |
9: 18,396,430 (GRCm39) |
N185S |
probably benign |
Het |
Mnx1 |
T |
C |
5: 29,679,851 (GRCm39) |
Q252R |
unknown |
Het |
Mroh3 |
A |
T |
1: 136,119,394 (GRCm39) |
L463Q |
possibly damaging |
Het |
Myom1 |
T |
C |
17: 71,406,967 (GRCm39) |
V1030A |
possibly damaging |
Het |
Or3a1d |
T |
C |
11: 74,237,640 (GRCm39) |
T257A |
probably benign |
Het |
Or5ak20 |
T |
C |
2: 85,184,114 (GRCm39) |
D52G |
probably benign |
Het |
Or5w1 |
T |
G |
2: 87,486,888 (GRCm39) |
I126L |
possibly damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Ranbp17 |
A |
G |
11: 33,167,419 (GRCm39) |
Y1015H |
probably benign |
Het |
Rasal1 |
C |
T |
5: 120,801,829 (GRCm39) |
T256I |
probably benign |
Het |
Rexo5 |
T |
A |
7: 119,423,002 (GRCm39) |
I278N |
probably damaging |
Het |
Rims2 |
T |
A |
15: 39,300,499 (GRCm39) |
S77T |
probably damaging |
Het |
Sdk2 |
C |
T |
11: 113,741,808 (GRCm39) |
A804T |
probably benign |
Het |
Slc24a2 |
T |
A |
4: 86,914,871 (GRCm39) |
I589F |
probably benign |
Het |
Slc25a38 |
T |
A |
9: 119,951,181 (GRCm39) |
I217K |
probably benign |
Het |
Slc5a7 |
T |
C |
17: 54,583,704 (GRCm39) |
T529A |
probably benign |
Het |
Spata22 |
T |
A |
11: 73,227,034 (GRCm39) |
S83T |
probably damaging |
Het |
Spata31e4 |
A |
T |
13: 50,854,414 (GRCm39) |
T91S |
possibly damaging |
Het |
Stac2 |
A |
T |
11: 97,934,324 (GRCm39) |
C127S |
possibly damaging |
Het |
Tep1 |
T |
C |
14: 51,062,259 (GRCm39) |
H2531R |
probably benign |
Het |
Trim60 |
T |
C |
8: 65,453,176 (GRCm39) |
T358A |
probably benign |
Het |
Unc13c |
T |
A |
9: 73,665,236 (GRCm39) |
M1048L |
probably benign |
Het |
Usp29 |
T |
C |
7: 6,965,074 (GRCm39) |
S306P |
probably damaging |
Het |
Zfp26 |
T |
C |
9: 20,356,203 (GRCm39) |
K35R |
probably benign |
Het |
Zfp462 |
T |
A |
4: 55,016,986 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Tmem151a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01913:Tmem151a
|
APN |
19 |
5,131,920 (GRCm39) |
missense |
probably benign |
0.36 |
IGL02708:Tmem151a
|
APN |
19 |
5,132,875 (GRCm39) |
nonsense |
probably null |
|
IGL02887:Tmem151a
|
APN |
19 |
5,132,993 (GRCm39) |
missense |
probably benign |
|
IGL03144:Tmem151a
|
APN |
19 |
5,135,400 (GRCm39) |
start codon destroyed |
probably benign |
0.01 |
R0395:Tmem151a
|
UTSW |
19 |
5,132,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R1732:Tmem151a
|
UTSW |
19 |
5,132,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:Tmem151a
|
UTSW |
19 |
5,132,966 (GRCm39) |
missense |
probably benign |
|
R4399:Tmem151a
|
UTSW |
19 |
5,133,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Tmem151a
|
UTSW |
19 |
5,121,862 (GRCm39) |
unclassified |
probably benign |
|
R6921:Tmem151a
|
UTSW |
19 |
5,133,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R7205:Tmem151a
|
UTSW |
19 |
5,132,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R7413:Tmem151a
|
UTSW |
19 |
5,132,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R7544:Tmem151a
|
UTSW |
19 |
5,121,895 (GRCm39) |
missense |
unknown |
|
R8017:Tmem151a
|
UTSW |
19 |
5,132,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R9662:Tmem151a
|
UTSW |
19 |
5,132,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R9709:Tmem151a
|
UTSW |
19 |
5,131,876 (GRCm39) |
nonsense |
probably null |
|
R9732:Tmem151a
|
UTSW |
19 |
5,131,937 (GRCm39) |
missense |
probably damaging |
0.96 |
R9786:Tmem151a
|
UTSW |
19 |
5,131,869 (GRCm39) |
missense |
probably damaging |
1.00 |
X0010:Tmem151a
|
UTSW |
19 |
5,133,014 (GRCm39) |
missense |
probably damaging |
1.00 |
|