Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
T |
A |
11: 110,201,059 (GRCm39) |
Y447F |
probably damaging |
Het |
Acaca |
A |
G |
11: 84,203,547 (GRCm39) |
|
probably benign |
Het |
Adam5 |
T |
C |
8: 25,305,125 (GRCm39) |
T110A |
probably benign |
Het |
Agtpbp1 |
T |
C |
13: 59,608,410 (GRCm39) |
M175V |
possibly damaging |
Het |
Akt1 |
T |
C |
12: 112,622,967 (GRCm39) |
N367S |
probably benign |
Het |
Ankrd61 |
T |
A |
5: 143,828,646 (GRCm39) |
T67S |
probably damaging |
Het |
Arl8a |
T |
C |
1: 135,080,610 (GRCm39) |
|
probably null |
Het |
Arvcf |
G |
A |
16: 18,221,783 (GRCm39) |
R736Q |
probably damaging |
Het |
Baz2a |
T |
A |
10: 127,959,979 (GRCm39) |
M1419K |
probably damaging |
Het |
Cep295 |
A |
T |
9: 15,244,661 (GRCm39) |
V1265E |
probably damaging |
Het |
Cfap299 |
A |
T |
5: 98,885,482 (GRCm39) |
I130F |
probably damaging |
Het |
Cyp2c29 |
A |
G |
19: 39,317,588 (GRCm39) |
D397G |
probably damaging |
Het |
Dlgap4 |
T |
C |
2: 156,591,267 (GRCm39) |
S818P |
probably benign |
Het |
Dnah2 |
A |
G |
11: 69,320,174 (GRCm39) |
I3965T |
probably damaging |
Het |
Dst |
A |
G |
1: 34,328,701 (GRCm39) |
T4590A |
probably damaging |
Het |
Eif1ad10 |
T |
C |
12: 88,216,476 (GRCm39) |
D132G |
unknown |
Het |
Fscb |
G |
T |
12: 64,519,906 (GRCm39) |
P520Q |
unknown |
Het |
Gli1 |
T |
A |
10: 127,167,225 (GRCm39) |
N676I |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,266,660 (GRCm39) |
I1916T |
probably damaging |
Het |
Igfals |
G |
A |
17: 25,100,579 (GRCm39) |
V557I |
possibly damaging |
Het |
Il7 |
A |
T |
3: 7,669,224 (GRCm39) |
V4D |
probably damaging |
Het |
Itgae |
T |
A |
11: 73,004,442 (GRCm39) |
I243N |
probably damaging |
Het |
Itpa |
T |
G |
2: 130,522,930 (GRCm39) |
S176A |
probably damaging |
Het |
Klhl13 |
T |
C |
X: 23,151,415 (GRCm39) |
D21G |
probably benign |
Het |
Krt26 |
T |
C |
11: 99,225,570 (GRCm39) |
K304E |
probably damaging |
Het |
Ly6g6e |
T |
C |
17: 35,296,159 (GRCm39) |
V10A |
probably benign |
Het |
Morc3 |
G |
A |
16: 93,659,324 (GRCm39) |
V411I |
probably damaging |
Het |
Mrpl32 |
G |
T |
13: 14,787,630 (GRCm39) |
|
probably benign |
Het |
Ncald |
G |
A |
15: 37,397,497 (GRCm39) |
A61V |
probably damaging |
Het |
Nek2 |
T |
C |
1: 191,559,320 (GRCm39) |
V275A |
probably benign |
Het |
Or12d12 |
T |
A |
17: 37,610,870 (GRCm39) |
T148S |
probably benign |
Het |
Or4f6 |
T |
C |
2: 111,838,668 (GRCm39) |
T288A |
possibly damaging |
Het |
Or5l13 |
T |
A |
2: 87,779,874 (GRCm39) |
R234S |
probably damaging |
Het |
Or5m10b |
T |
A |
2: 85,699,306 (GRCm39) |
Y123* |
probably null |
Het |
Pgam5 |
T |
C |
5: 110,413,465 (GRCm39) |
Y210C |
probably damaging |
Het |
Phf5a |
T |
C |
15: 81,754,628 (GRCm39) |
N50D |
probably benign |
Het |
Prl7d1 |
A |
G |
13: 27,900,651 (GRCm39) |
M1T |
probably null |
Het |
Sacs |
A |
G |
14: 61,429,735 (GRCm39) |
K595R |
possibly damaging |
Het |
Scyl3 |
A |
G |
1: 163,778,206 (GRCm39) |
N448S |
probably benign |
Het |
Sgsh |
A |
G |
11: 119,241,773 (GRCm39) |
L111P |
probably damaging |
Het |
Smg1 |
T |
C |
7: 117,753,885 (GRCm39) |
|
probably benign |
Het |
Taar1 |
T |
C |
10: 23,796,482 (GRCm39) |
L60P |
probably damaging |
Het |
Tmem51 |
T |
C |
4: 141,759,059 (GRCm39) |
T230A |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,151,301 (GRCm39) |
V623A |
probably damaging |
Het |
Usp34 |
C |
T |
11: 23,439,033 (GRCm39) |
P3532S |
possibly damaging |
Het |
Vipr2 |
T |
C |
12: 116,099,724 (GRCm39) |
|
probably benign |
Het |
Vmn2r16 |
T |
C |
5: 109,488,177 (GRCm39) |
M350T |
probably benign |
Het |
Vmn2r22 |
T |
C |
6: 123,614,339 (GRCm39) |
E417G |
possibly damaging |
Het |
Vmn2r9 |
C |
A |
5: 108,995,701 (GRCm39) |
V316F |
probably benign |
Het |
Zfp53 |
C |
T |
17: 21,728,893 (GRCm39) |
P309S |
probably damaging |
Het |
|
Other mutations in Serpinb9g |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01655:Serpinb9g
|
APN |
13 |
33,679,088 (GRCm39) |
nonsense |
probably null |
|
IGL02346:Serpinb9g
|
APN |
13 |
33,670,514 (GRCm39) |
start codon destroyed |
probably benign |
0.12 |
IGL02665:Serpinb9g
|
APN |
13 |
33,679,086 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02936:Serpinb9g
|
APN |
13 |
33,678,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1611:Serpinb9g
|
UTSW |
13 |
33,676,857 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4060:Serpinb9g
|
UTSW |
13 |
33,679,089 (GRCm39) |
missense |
probably benign |
0.19 |
R4505:Serpinb9g
|
UTSW |
13 |
33,670,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R6399:Serpinb9g
|
UTSW |
13 |
33,676,834 (GRCm39) |
missense |
probably benign |
|
R6843:Serpinb9g
|
UTSW |
13 |
33,676,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R6844:Serpinb9g
|
UTSW |
13 |
33,670,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R6942:Serpinb9g
|
UTSW |
13 |
33,678,888 (GRCm39) |
missense |
probably benign |
0.03 |
R7319:Serpinb9g
|
UTSW |
13 |
33,672,543 (GRCm39) |
nonsense |
probably null |
|
R7466:Serpinb9g
|
UTSW |
13 |
33,679,150 (GRCm39) |
missense |
probably benign |
|
R7470:Serpinb9g
|
UTSW |
13 |
33,670,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R8350:Serpinb9g
|
UTSW |
13 |
33,676,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R8531:Serpinb9g
|
UTSW |
13 |
33,676,896 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8555:Serpinb9g
|
UTSW |
13 |
33,676,796 (GRCm39) |
missense |
probably benign |
0.02 |
R8743:Serpinb9g
|
UTSW |
13 |
33,678,931 (GRCm39) |
missense |
probably benign |
|
R8918:Serpinb9g
|
UTSW |
13 |
33,679,131 (GRCm39) |
missense |
probably benign |
0.00 |
R9542:Serpinb9g
|
UTSW |
13 |
33,679,141 (GRCm39) |
missense |
probably benign |
0.12 |
|