Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930449A18Rik |
A |
G |
3: 59,754,199 (GRCm39) |
|
noncoding transcript |
Het |
Aadacl2fm2 |
T |
C |
3: 59,659,387 (GRCm39) |
F280S |
probably damaging |
Het |
Adamts7 |
G |
A |
9: 90,077,904 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
A |
C |
13: 81,641,029 (GRCm39) |
S3335R |
unknown |
Het |
Armc6 |
G |
A |
8: 70,677,943 (GRCm39) |
L129F |
probably benign |
Het |
B4galt3 |
C |
A |
1: 171,101,613 (GRCm39) |
H196N |
probably damaging |
Het |
Bltp1 |
C |
T |
3: 37,042,296 (GRCm39) |
Q2761* |
probably null |
Het |
Cdh19 |
G |
A |
1: 110,817,442 (GRCm39) |
Q767* |
probably null |
Het |
Cep120 |
G |
A |
18: 53,818,957 (GRCm39) |
|
probably null |
Het |
Dhx38 |
C |
T |
8: 110,279,763 (GRCm39) |
V976I |
probably damaging |
Het |
Efr3a |
T |
A |
15: 65,738,629 (GRCm39) |
F753I |
possibly damaging |
Het |
Hspb7 |
A |
T |
4: 141,151,329 (GRCm39) |
E157V |
probably damaging |
Het |
Irx6 |
A |
G |
8: 93,405,029 (GRCm39) |
E299G |
probably damaging |
Het |
Jhy |
T |
A |
9: 40,828,440 (GRCm39) |
N489Y |
possibly damaging |
Het |
Klhl22 |
T |
C |
16: 17,607,137 (GRCm39) |
V481A |
possibly damaging |
Het |
Mapk13 |
A |
G |
17: 28,996,539 (GRCm39) |
|
probably null |
Het |
Meis1 |
A |
T |
11: 18,960,656 (GRCm39) |
|
probably benign |
Het |
Nlrp14 |
A |
G |
7: 106,797,012 (GRCm39) |
K301E |
probably benign |
Het |
Nol10 |
T |
C |
12: 17,429,293 (GRCm39) |
Y340H |
probably damaging |
Het |
Or2k2 |
T |
C |
4: 58,785,153 (GRCm39) |
S190G |
probably benign |
Het |
Paqr3 |
T |
C |
5: 97,256,150 (GRCm39) |
S75G |
probably damaging |
Het |
Pdgfa |
T |
C |
5: 138,972,061 (GRCm39) |
T113A |
probably damaging |
Het |
Phactr2 |
A |
G |
10: 13,129,564 (GRCm39) |
S235P |
probably damaging |
Het |
Psph |
T |
G |
5: 129,848,654 (GRCm39) |
K9T |
probably benign |
Het |
Ptpn21 |
T |
C |
12: 98,644,852 (GRCm39) |
Y1163C |
probably damaging |
Het |
Scaf8 |
T |
C |
17: 3,221,470 (GRCm39) |
L319P |
unknown |
Het |
Slc4a7 |
C |
T |
14: 14,733,775 (GRCm38) |
R62W |
probably damaging |
Het |
Slc6a3 |
C |
A |
13: 73,709,031 (GRCm39) |
C318* |
probably null |
Het |
Speer3 |
C |
G |
5: 13,846,394 (GRCm39) |
A238G |
possibly damaging |
Het |
Taf1c |
A |
C |
8: 120,326,055 (GRCm39) |
S602R |
possibly damaging |
Het |
Tiam2 |
A |
G |
17: 3,464,958 (GRCm39) |
D229G |
probably benign |
Het |
Tor1a |
A |
G |
2: 30,857,382 (GRCm39) |
|
probably benign |
Het |
Trim45 |
T |
C |
3: 100,830,502 (GRCm39) |
I92T |
probably damaging |
Het |
Ttll8 |
G |
A |
15: 88,798,384 (GRCm39) |
P784S |
possibly damaging |
Het |
Tubg1 |
G |
T |
11: 101,016,190 (GRCm39) |
|
probably null |
Het |
Vmn1r178 |
A |
T |
7: 23,593,447 (GRCm39) |
N92I |
probably damaging |
Het |
Vmn2r87 |
A |
G |
10: 130,315,676 (GRCm39) |
V130A |
probably benign |
Het |
Wdr46 |
A |
G |
17: 34,160,120 (GRCm39) |
|
probably benign |
Het |
Yme1l1 |
A |
G |
2: 23,050,223 (GRCm39) |
H18R |
possibly damaging |
Het |
Zfp263 |
T |
A |
16: 3,562,770 (GRCm39) |
|
probably benign |
Het |
Zfp534 |
T |
C |
4: 147,760,015 (GRCm39) |
D218G |
probably benign |
Het |
|
Other mutations in Zscan12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02864:Zscan12
|
APN |
13 |
21,552,730 (GRCm39) |
missense |
probably benign |
0.02 |
PIT4480001:Zscan12
|
UTSW |
13 |
21,552,744 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0122:Zscan12
|
UTSW |
13 |
21,553,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Zscan12
|
UTSW |
13 |
21,550,813 (GRCm39) |
missense |
probably benign |
0.00 |
R1639:Zscan12
|
UTSW |
13 |
21,553,156 (GRCm39) |
missense |
probably damaging |
0.99 |
R2182:Zscan12
|
UTSW |
13 |
21,552,961 (GRCm39) |
missense |
probably benign |
0.33 |
R2931:Zscan12
|
UTSW |
13 |
21,548,187 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3930:Zscan12
|
UTSW |
13 |
21,552,800 (GRCm39) |
missense |
probably benign |
0.18 |
R4461:Zscan12
|
UTSW |
13 |
21,550,789 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4545:Zscan12
|
UTSW |
13 |
21,550,875 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5353:Zscan12
|
UTSW |
13 |
21,548,178 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6580:Zscan12
|
UTSW |
13 |
21,553,328 (GRCm39) |
missense |
probably damaging |
0.99 |
R6734:Zscan12
|
UTSW |
13 |
21,552,966 (GRCm39) |
nonsense |
probably null |
|
R7462:Zscan12
|
UTSW |
13 |
21,553,457 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7505:Zscan12
|
UTSW |
13 |
21,552,756 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7822:Zscan12
|
UTSW |
13 |
21,553,374 (GRCm39) |
missense |
probably damaging |
0.99 |
R8028:Zscan12
|
UTSW |
13 |
21,553,022 (GRCm39) |
missense |
probably benign |
0.01 |
R8056:Zscan12
|
UTSW |
13 |
21,553,492 (GRCm39) |
missense |
probably benign |
0.29 |
R8161:Zscan12
|
UTSW |
13 |
21,547,897 (GRCm39) |
missense |
probably benign |
0.01 |
R8784:Zscan12
|
UTSW |
13 |
21,547,991 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8794:Zscan12
|
UTSW |
13 |
21,547,847 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9716:Zscan12
|
UTSW |
13 |
21,547,938 (GRCm39) |
missense |
possibly damaging |
0.68 |
|