Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930566N20Rik |
C |
A |
3: 156,914,039 (GRCm39) |
|
probably benign |
Het |
6330409D20Rik |
T |
G |
2: 32,630,698 (GRCm39) |
|
probably benign |
Het |
Als2cl |
A |
G |
9: 110,723,407 (GRCm39) |
K659E |
probably benign |
Het |
Bbx |
G |
A |
16: 50,022,854 (GRCm39) |
T702I |
probably damaging |
Het |
Bcas3 |
A |
G |
11: 85,448,263 (GRCm39) |
D405G |
probably damaging |
Het |
Brpf3 |
A |
G |
17: 29,026,370 (GRCm39) |
Y481C |
probably benign |
Het |
Csnk1g1 |
T |
A |
9: 65,909,533 (GRCm39) |
Y217N |
probably damaging |
Het |
Cyp4f37 |
G |
T |
17: 32,846,825 (GRCm39) |
V171L |
possibly damaging |
Het |
Dock8 |
G |
A |
19: 25,178,350 (GRCm39) |
|
probably null |
Het |
Extl3 |
C |
A |
14: 65,313,788 (GRCm39) |
G465W |
probably damaging |
Het |
Fbxo10 |
A |
G |
4: 45,046,349 (GRCm39) |
I587T |
possibly damaging |
Het |
Fstl5 |
A |
C |
3: 76,566,959 (GRCm39) |
|
probably benign |
Het |
Gabbr2 |
T |
C |
4: 46,667,547 (GRCm39) |
N866S |
probably benign |
Het |
Gm4871 |
T |
A |
5: 144,969,388 (GRCm39) |
K44* |
probably null |
Het |
Hnrnpul1 |
T |
C |
7: 25,421,766 (GRCm39) |
|
probably benign |
Het |
Jup |
A |
G |
11: 100,274,215 (GRCm39) |
|
probably benign |
Het |
Mccc2 |
A |
T |
13: 100,136,783 (GRCm39) |
H57Q |
probably benign |
Het |
Myo1a |
A |
T |
10: 127,546,094 (GRCm39) |
D239V |
probably damaging |
Het |
Ncapd3 |
T |
A |
9: 26,974,612 (GRCm39) |
S695T |
probably benign |
Het |
Ncor1 |
A |
T |
11: 62,249,743 (GRCm39) |
S1052T |
probably damaging |
Het |
Or5k8 |
A |
G |
16: 58,644,169 (GRCm39) |
I301T |
probably benign |
Het |
Or7g12 |
T |
A |
9: 18,899,621 (GRCm39) |
N112K |
possibly damaging |
Het |
Or8c10 |
C |
T |
9: 38,279,603 (GRCm39) |
H244Y |
probably damaging |
Het |
Pcnx3 |
A |
T |
19: 5,729,414 (GRCm39) |
I526K |
probably damaging |
Het |
Pcnx4 |
A |
G |
12: 72,621,102 (GRCm39) |
D974G |
possibly damaging |
Het |
Peg3 |
T |
C |
7: 6,714,001 (GRCm39) |
E407G |
probably damaging |
Het |
Polk |
A |
G |
13: 96,641,059 (GRCm39) |
V166A |
probably damaging |
Het |
Prkar2a |
A |
G |
9: 108,610,322 (GRCm39) |
I184V |
probably damaging |
Het |
Ptpra |
T |
C |
2: 30,333,362 (GRCm39) |
S64P |
probably damaging |
Het |
Rbsn |
A |
G |
6: 92,166,340 (GRCm39) |
L768P |
probably damaging |
Het |
Ripk3 |
C |
T |
14: 56,023,482 (GRCm39) |
|
probably null |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Sar1b |
T |
C |
11: 51,680,020 (GRCm39) |
|
probably benign |
Het |
Slx |
A |
T |
X: 26,489,755 (GRCm39) |
W89R |
probably benign |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Svep1 |
T |
C |
4: 58,070,104 (GRCm39) |
I2561V |
probably benign |
Het |
Tasor2 |
T |
C |
13: 3,624,721 (GRCm39) |
D1743G |
probably benign |
Het |
Tm7sf3 |
A |
G |
6: 146,525,208 (GRCm39) |
L79P |
possibly damaging |
Het |
Trub1 |
A |
T |
19: 57,441,379 (GRCm39) |
M1L |
probably benign |
Het |
Unc80 |
A |
G |
1: 66,651,386 (GRCm39) |
D1577G |
possibly damaging |
Het |
Vat1 |
A |
T |
11: 101,351,405 (GRCm39) |
M312K |
possibly damaging |
Het |
Vmn1r17 |
T |
C |
6: 57,337,787 (GRCm39) |
I193V |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,875,732 (GRCm39) |
I2706V |
possibly damaging |
Het |
Wls |
T |
C |
3: 159,612,890 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Zfp955b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00537:Zfp955b
|
APN |
17 |
33,521,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02126:Zfp955b
|
APN |
17 |
33,521,238 (GRCm39) |
nonsense |
probably null |
|
IGL02237:Zfp955b
|
APN |
17 |
33,520,893 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02587:Zfp955b
|
APN |
17 |
33,519,624 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02971:Zfp955b
|
APN |
17 |
33,519,940 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03034:Zfp955b
|
APN |
17 |
33,521,142 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03493:Zfp955b
|
APN |
17 |
33,521,519 (GRCm39) |
missense |
probably benign |
0.35 |
R0269:Zfp955b
|
UTSW |
17 |
33,524,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R0373:Zfp955b
|
UTSW |
17 |
33,521,496 (GRCm39) |
missense |
probably benign |
|
R0617:Zfp955b
|
UTSW |
17 |
33,524,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R0684:Zfp955b
|
UTSW |
17 |
33,521,947 (GRCm39) |
missense |
probably benign |
0.00 |
R1778:Zfp955b
|
UTSW |
17 |
33,521,788 (GRCm39) |
missense |
probably benign |
0.07 |
R1874:Zfp955b
|
UTSW |
17 |
33,524,427 (GRCm39) |
missense |
probably benign |
0.10 |
R3893:Zfp955b
|
UTSW |
17 |
33,521,968 (GRCm39) |
missense |
probably benign |
0.01 |
R3938:Zfp955b
|
UTSW |
17 |
33,524,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R4082:Zfp955b
|
UTSW |
17 |
33,521,129 (GRCm39) |
missense |
probably benign |
0.08 |
R4672:Zfp955b
|
UTSW |
17 |
33,524,233 (GRCm39) |
unclassified |
probably benign |
|
R4956:Zfp955b
|
UTSW |
17 |
33,524,209 (GRCm39) |
unclassified |
probably benign |
|
R4998:Zfp955b
|
UTSW |
17 |
33,524,125 (GRCm39) |
unclassified |
probably benign |
|
R5276:Zfp955b
|
UTSW |
17 |
33,522,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R5341:Zfp955b
|
UTSW |
17 |
33,524,095 (GRCm39) |
unclassified |
probably benign |
|
R5558:Zfp955b
|
UTSW |
17 |
33,521,161 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6086:Zfp955b
|
UTSW |
17 |
33,521,478 (GRCm39) |
missense |
probably benign |
|
R6170:Zfp955b
|
UTSW |
17 |
33,521,084 (GRCm39) |
missense |
probably benign |
0.00 |
R6306:Zfp955b
|
UTSW |
17 |
33,522,160 (GRCm39) |
missense |
probably benign |
0.07 |
R6519:Zfp955b
|
UTSW |
17 |
33,521,051 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9286:Zfp955b
|
UTSW |
17 |
33,521,683 (GRCm39) |
missense |
probably benign |
0.04 |
|