Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
A |
T |
9: 57,165,894 (GRCm39) |
V160E |
probably damaging |
Het |
Abhd8 |
C |
T |
8: 71,910,894 (GRCm39) |
G305S |
probably benign |
Het |
Adamts20 |
A |
G |
15: 94,231,579 (GRCm39) |
V870A |
probably benign |
Het |
Agl |
A |
G |
3: 116,551,886 (GRCm39) |
|
probably null |
Het |
Cav3 |
A |
T |
6: 112,449,147 (GRCm39) |
D55V |
probably damaging |
Het |
Ccser2 |
T |
A |
14: 36,648,831 (GRCm39) |
D556V |
probably damaging |
Het |
Cdc20b |
T |
C |
13: 113,215,193 (GRCm39) |
Y254H |
probably benign |
Het |
Commd8 |
A |
G |
5: 72,317,223 (GRCm39) |
L182S |
probably damaging |
Het |
Cyp1b1 |
G |
A |
17: 80,020,728 (GRCm39) |
A338V |
probably damaging |
Het |
Def8 |
C |
A |
8: 124,186,798 (GRCm39) |
D459E |
unknown |
Het |
Dennd5b |
T |
C |
6: 148,943,214 (GRCm39) |
Y554C |
probably damaging |
Het |
Dnah7c |
A |
T |
1: 46,665,460 (GRCm39) |
|
probably null |
Het |
Dnajc5b |
T |
A |
3: 19,633,181 (GRCm39) |
C135S |
probably benign |
Het |
Dnpep |
G |
A |
1: 75,293,890 (GRCm39) |
|
probably benign |
Het |
Drc1 |
C |
T |
5: 30,507,856 (GRCm39) |
Q293* |
probably null |
Het |
Glmp |
A |
G |
3: 88,233,077 (GRCm39) |
S72G |
probably benign |
Het |
Gm5431 |
A |
T |
11: 48,779,285 (GRCm39) |
S546T |
probably benign |
Het |
Gnptab |
T |
A |
10: 88,247,782 (GRCm39) |
C70S |
probably benign |
Het |
Gpr83 |
G |
A |
9: 14,778,170 (GRCm39) |
R180Q |
probably damaging |
Het |
Gucy1a1 |
A |
T |
3: 82,016,112 (GRCm39) |
L292Q |
possibly damaging |
Het |
Gzmd |
T |
C |
14: 56,368,720 (GRCm39) |
D58G |
probably damaging |
Het |
Hoxa10 |
A |
G |
6: 52,211,245 (GRCm39) |
S224P |
possibly damaging |
Het |
Hoxa13 |
G |
A |
6: 52,237,247 (GRCm39) |
|
probably benign |
Het |
Igsf6 |
A |
G |
7: 120,667,548 (GRCm39) |
V156A |
probably benign |
Het |
Il6st |
A |
T |
13: 112,639,338 (GRCm39) |
I649F |
probably damaging |
Het |
Kcnh3 |
G |
A |
15: 99,131,147 (GRCm39) |
V507M |
probably damaging |
Het |
Lgr5 |
A |
G |
10: 115,307,899 (GRCm39) |
I253T |
probably damaging |
Het |
Met |
T |
A |
6: 17,491,406 (GRCm39) |
V56D |
possibly damaging |
Het |
Mettl22 |
A |
T |
16: 8,303,764 (GRCm39) |
I277F |
possibly damaging |
Het |
Nadsyn1 |
G |
A |
7: 143,359,740 (GRCm39) |
R411W |
probably damaging |
Het |
Nrros |
T |
G |
16: 31,962,346 (GRCm39) |
E557A |
probably benign |
Het |
Or10ak14 |
A |
T |
4: 118,611,254 (GRCm39) |
H162Q |
probably benign |
Het |
Or5w1 |
T |
C |
2: 87,486,813 (GRCm39) |
I151V |
not run |
Het |
Or8j3b |
C |
T |
2: 86,205,604 (GRCm39) |
V51M |
possibly damaging |
Het |
Polr1b |
C |
A |
2: 128,967,464 (GRCm39) |
F952L |
probably damaging |
Het |
Ppp1r3a |
A |
G |
6: 14,754,977 (GRCm39) |
V90A |
probably benign |
Het |
Prmt9 |
T |
A |
8: 78,285,814 (GRCm39) |
|
probably null |
Het |
Rapgef4 |
T |
A |
2: 72,028,739 (GRCm39) |
N385K |
possibly damaging |
Het |
Rbm28 |
G |
A |
6: 29,164,627 (GRCm39) |
|
probably benign |
Het |
Rhobtb3 |
A |
T |
13: 76,065,934 (GRCm39) |
S150T |
probably damaging |
Het |
Serpinb6b |
T |
C |
13: 33,161,512 (GRCm39) |
V195A |
probably benign |
Het |
Sesn1 |
T |
A |
10: 41,770,054 (GRCm39) |
I99N |
probably damaging |
Het |
Setd1b |
G |
A |
5: 123,296,815 (GRCm39) |
|
probably benign |
Het |
Slc22a19 |
T |
A |
19: 7,681,360 (GRCm39) |
|
probably null |
Het |
Slc9a4 |
T |
C |
1: 40,640,123 (GRCm39) |
I305T |
probably damaging |
Het |
Smg6 |
T |
A |
11: 74,884,687 (GRCm39) |
N3K |
unknown |
Het |
Spta1 |
C |
A |
1: 174,023,547 (GRCm39) |
Y651* |
probably null |
Het |
Tatdn3 |
G |
A |
1: 190,791,053 (GRCm39) |
P74S |
probably benign |
Het |
Tet2 |
C |
T |
3: 133,186,056 (GRCm39) |
R1127Q |
possibly damaging |
Het |
Tgfbi |
T |
A |
13: 56,780,657 (GRCm39) |
|
probably null |
Het |
Tmprss9 |
A |
G |
10: 80,733,903 (GRCm39) |
|
probably null |
Het |
Tox4 |
T |
C |
14: 52,517,299 (GRCm39) |
Y10H |
probably damaging |
Het |
Trappc10 |
A |
T |
10: 78,046,679 (GRCm39) |
S407T |
probably damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,708,336 (GRCm39) |
C24R |
probably damaging |
Het |
Wdr24 |
C |
A |
17: 26,046,070 (GRCm39) |
A465D |
probably benign |
Het |
Wfdc8 |
A |
G |
2: 164,439,594 (GRCm39) |
S263P |
unknown |
Het |
Zc3h15 |
T |
A |
2: 83,488,476 (GRCm39) |
I138N |
possibly damaging |
Het |
|
Other mutations in Pih1d2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01819:Pih1d2
|
APN |
9 |
50,533,177 (GRCm39) |
missense |
probably benign |
0.09 |
FR4449:Pih1d2
|
UTSW |
9 |
50,532,927 (GRCm39) |
frame shift |
probably null |
|
R0390:Pih1d2
|
UTSW |
9 |
50,532,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R0443:Pih1d2
|
UTSW |
9 |
50,532,403 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1570:Pih1d2
|
UTSW |
9 |
50,532,479 (GRCm39) |
missense |
probably benign |
0.06 |
R1874:Pih1d2
|
UTSW |
9 |
50,532,245 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2207:Pih1d2
|
UTSW |
9 |
50,532,379 (GRCm39) |
missense |
probably benign |
0.17 |
R4667:Pih1d2
|
UTSW |
9 |
50,532,252 (GRCm39) |
nonsense |
probably null |
|
R5806:Pih1d2
|
UTSW |
9 |
50,529,750 (GRCm39) |
unclassified |
probably benign |
|
R5811:Pih1d2
|
UTSW |
9 |
50,532,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R5949:Pih1d2
|
UTSW |
9 |
50,536,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R6156:Pih1d2
|
UTSW |
9 |
50,532,452 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6416:Pih1d2
|
UTSW |
9 |
50,529,909 (GRCm39) |
missense |
probably benign |
0.00 |
R6711:Pih1d2
|
UTSW |
9 |
50,529,310 (GRCm39) |
start codon destroyed |
probably null |
|
R7052:Pih1d2
|
UTSW |
9 |
50,533,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R7557:Pih1d2
|
UTSW |
9 |
50,536,216 (GRCm39) |
missense |
probably damaging |
0.99 |
R7661:Pih1d2
|
UTSW |
9 |
50,529,558 (GRCm39) |
critical splice donor site |
probably null |
|
R8295:Pih1d2
|
UTSW |
9 |
50,532,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R8978:Pih1d2
|
UTSW |
9 |
50,536,232 (GRCm39) |
missense |
probably benign |
0.43 |
R9147:Pih1d2
|
UTSW |
9 |
50,532,321 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9401:Pih1d2
|
UTSW |
9 |
50,529,905 (GRCm39) |
missense |
probably damaging |
1.00 |
|