Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933411K16Rik |
T |
C |
19: 42,040,962 (GRCm39) |
I31T |
possibly damaging |
Het |
Abca13 |
A |
G |
11: 9,206,197 (GRCm39) |
I166V |
probably damaging |
Het |
Acaa2 |
G |
T |
18: 74,931,517 (GRCm39) |
V238L |
probably benign |
Het |
Ahsg |
A |
T |
16: 22,717,805 (GRCm39) |
I296F |
possibly damaging |
Het |
Aspm |
T |
A |
1: 139,415,027 (GRCm39) |
V1436D |
probably damaging |
Het |
Ate1 |
A |
T |
7: 130,115,563 (GRCm39) |
|
probably benign |
Het |
Atosa |
T |
A |
9: 74,911,570 (GRCm39) |
Y14N |
probably damaging |
Het |
Atp1a4 |
A |
T |
1: 172,059,627 (GRCm39) |
|
probably benign |
Het |
Aurkc |
A |
T |
7: 7,005,402 (GRCm39) |
I223L |
possibly damaging |
Het |
Bckdha |
G |
T |
7: 25,341,210 (GRCm39) |
D50E |
probably benign |
Het |
Brf2 |
C |
T |
8: 27,614,059 (GRCm39) |
E376K |
probably benign |
Het |
Cdk9 |
C |
A |
2: 32,599,813 (GRCm39) |
L141F |
possibly damaging |
Het |
Cgn |
A |
C |
3: 94,678,024 (GRCm39) |
|
probably benign |
Het |
Clcn1 |
G |
A |
6: 42,282,509 (GRCm39) |
V526I |
probably damaging |
Het |
Cnot2 |
A |
G |
10: 116,334,141 (GRCm39) |
V343A |
possibly damaging |
Het |
Commd2 |
A |
T |
3: 57,554,116 (GRCm39) |
V195D |
possibly damaging |
Het |
Cubn |
C |
T |
2: 13,365,063 (GRCm39) |
|
probably null |
Het |
Eif2ak4 |
C |
T |
2: 118,266,666 (GRCm39) |
T729M |
probably damaging |
Het |
Elac1 |
A |
T |
18: 73,871,954 (GRCm39) |
V347E |
probably damaging |
Het |
Fam20c |
G |
A |
5: 138,793,241 (GRCm39) |
R454Q |
probably damaging |
Het |
Faxc |
C |
T |
4: 21,958,608 (GRCm39) |
S255L |
probably benign |
Het |
Fem1al |
C |
A |
11: 29,774,515 (GRCm39) |
R314L |
probably damaging |
Het |
Foxj1 |
T |
C |
11: 116,224,908 (GRCm39) |
D153G |
possibly damaging |
Het |
Gm6605 |
C |
A |
7: 38,147,699 (GRCm39) |
|
noncoding transcript |
Het |
Lmo7 |
T |
A |
14: 102,114,295 (GRCm39) |
Y12* |
probably null |
Het |
Matn3 |
T |
G |
12: 9,013,594 (GRCm39) |
C425W |
probably damaging |
Het |
Mmd2 |
A |
T |
5: 142,550,668 (GRCm39) |
M190K |
probably benign |
Het |
Morn2 |
A |
T |
17: 80,603,026 (GRCm39) |
T102S |
probably damaging |
Het |
Nr3c2 |
A |
C |
8: 77,912,518 (GRCm39) |
T710P |
probably benign |
Het |
Nrros |
C |
A |
16: 31,962,903 (GRCm39) |
L343F |
probably damaging |
Het |
Ntrk2 |
C |
T |
13: 59,276,000 (GRCm39) |
Q767* |
probably null |
Het |
Or2h2c |
G |
C |
17: 37,422,347 (GRCm39) |
L176V |
probably benign |
Het |
Or4k47 |
C |
T |
2: 111,452,264 (GRCm39) |
D52N |
possibly damaging |
Het |
Plekhf2 |
C |
T |
4: 10,991,330 (GRCm39) |
R4H |
probably benign |
Het |
Ppox |
A |
G |
1: 171,105,387 (GRCm39) |
|
probably benign |
Het |
Qprt |
T |
A |
7: 126,708,248 (GRCm39) |
D61V |
probably damaging |
Het |
Reln |
A |
G |
5: 22,215,148 (GRCm39) |
V1101A |
probably benign |
Het |
Sbno1 |
T |
C |
5: 124,548,202 (GRCm39) |
N124D |
probably damaging |
Het |
Scx |
C |
T |
15: 76,342,295 (GRCm39) |
P165L |
probably benign |
Het |
Sema6d |
T |
C |
2: 124,496,055 (GRCm39) |
|
probably benign |
Het |
Serf2 |
T |
C |
2: 121,281,336 (GRCm39) |
F92L |
probably benign |
Het |
Synpo2 |
A |
T |
3: 122,910,936 (GRCm39) |
N236K |
probably damaging |
Het |
Tbc1d32 |
C |
A |
10: 56,100,736 (GRCm39) |
D81Y |
probably benign |
Het |
Terf2 |
G |
A |
8: 107,809,622 (GRCm39) |
T232I |
possibly damaging |
Het |
Tpd52l2 |
A |
G |
2: 181,143,744 (GRCm39) |
E50G |
probably damaging |
Het |
Tprn |
A |
G |
2: 25,154,210 (GRCm39) |
E504G |
probably damaging |
Het |
Tufm |
G |
T |
7: 126,086,654 (GRCm39) |
R12L |
probably benign |
Het |
Vmn2r8 |
A |
G |
5: 108,947,195 (GRCm39) |
F519S |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,145,590 (GRCm39) |
V89A |
probably benign |
Het |
Wnt3 |
T |
C |
11: 103,703,207 (GRCm39) |
I230T |
possibly damaging |
Het |
Zan |
A |
T |
5: 137,466,693 (GRCm39) |
F388Y |
probably damaging |
Het |
Zfp474 |
C |
T |
18: 52,771,421 (GRCm39) |
L25F |
probably benign |
Het |
|
Other mutations in Fam209 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Fam209
|
APN |
2 |
172,316,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R0147:Fam209
|
UTSW |
2 |
172,315,900 (GRCm39) |
missense |
probably damaging |
0.99 |
R0148:Fam209
|
UTSW |
2 |
172,315,900 (GRCm39) |
missense |
probably damaging |
0.99 |
R0558:Fam209
|
UTSW |
2 |
172,314,758 (GRCm39) |
missense |
probably benign |
0.01 |
R0584:Fam209
|
UTSW |
2 |
172,316,081 (GRCm39) |
missense |
probably benign |
0.00 |
R0882:Fam209
|
UTSW |
2 |
172,314,555 (GRCm39) |
missense |
probably benign |
|
R2001:Fam209
|
UTSW |
2 |
172,314,689 (GRCm39) |
missense |
probably benign |
0.09 |
R2002:Fam209
|
UTSW |
2 |
172,314,689 (GRCm39) |
missense |
probably benign |
0.09 |
R3725:Fam209
|
UTSW |
2 |
172,315,915 (GRCm39) |
missense |
probably benign |
0.02 |
R3726:Fam209
|
UTSW |
2 |
172,315,915 (GRCm39) |
missense |
probably benign |
0.02 |
R3892:Fam209
|
UTSW |
2 |
172,314,618 (GRCm39) |
missense |
probably damaging |
0.98 |
R6697:Fam209
|
UTSW |
2 |
172,316,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R7051:Fam209
|
UTSW |
2 |
172,315,969 (GRCm39) |
missense |
probably damaging |
0.97 |
R7052:Fam209
|
UTSW |
2 |
172,314,751 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8160:Fam209
|
UTSW |
2 |
172,314,645 (GRCm39) |
missense |
possibly damaging |
0.94 |
|