Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
G |
T |
5: 8,978,578 (GRCm39) |
|
probably null |
Het |
Adam29 |
A |
G |
8: 56,325,224 (GRCm39) |
V410A |
possibly damaging |
Het |
Adamts3 |
T |
C |
5: 89,850,815 (GRCm39) |
T575A |
probably damaging |
Het |
Ankmy1 |
T |
C |
1: 92,804,353 (GRCm39) |
K877E |
possibly damaging |
Het |
Arpin |
A |
T |
7: 79,581,615 (GRCm39) |
I35N |
possibly damaging |
Het |
BC030500 |
T |
C |
8: 59,365,388 (GRCm39) |
I13T |
unknown |
Het |
Bcas1 |
T |
C |
2: 170,248,220 (GRCm39) |
N234D |
possibly damaging |
Het |
Clca3a2 |
C |
T |
3: 144,783,668 (GRCm39) |
G649E |
probably benign |
Het |
Cnot2 |
A |
T |
10: 116,322,181 (GRCm39) |
L516Q |
probably damaging |
Het |
Ctdp1 |
C |
A |
18: 80,512,494 (GRCm39) |
V90L |
probably benign |
Het |
Cyb5b |
A |
G |
8: 107,896,552 (GRCm39) |
Y91C |
possibly damaging |
Het |
Cystm1 |
T |
C |
18: 36,526,303 (GRCm39) |
|
probably benign |
Het |
Dnhd1 |
C |
A |
7: 105,327,231 (GRCm39) |
Q727K |
probably damaging |
Het |
Dpf3 |
G |
A |
12: 83,397,625 (GRCm39) |
R80C |
probably damaging |
Het |
Ehmt2 |
C |
T |
17: 35,127,667 (GRCm39) |
T882M |
probably damaging |
Het |
Fam136a |
A |
G |
6: 86,345,795 (GRCm39) |
K104R |
probably benign |
Het |
Fcgbp |
T |
C |
7: 27,793,614 (GRCm39) |
V1172A |
probably benign |
Het |
Foxc1 |
C |
T |
13: 31,991,548 (GRCm39) |
Q120* |
probably null |
Het |
Grin1 |
G |
A |
2: 25,188,323 (GRCm39) |
R448C |
probably damaging |
Het |
Igsf10 |
G |
A |
3: 59,238,949 (GRCm39) |
P411S |
probably damaging |
Het |
Irgq |
T |
A |
7: 24,233,165 (GRCm39) |
D335E |
probably benign |
Het |
Kndc1 |
A |
G |
7: 139,503,960 (GRCm39) |
Y1088C |
probably damaging |
Het |
Llgl1 |
A |
G |
11: 60,602,947 (GRCm39) |
E874G |
probably damaging |
Het |
Lrp8 |
A |
G |
4: 107,704,661 (GRCm39) |
N168D |
probably benign |
Het |
Lyst |
T |
A |
13: 13,824,973 (GRCm39) |
C1529* |
probably null |
Het |
Mau2 |
A |
T |
8: 70,495,242 (GRCm39) |
Y32N |
probably damaging |
Het |
Mios |
T |
A |
6: 8,227,998 (GRCm39) |
N638K |
probably benign |
Het |
Mki67 |
A |
T |
7: 135,300,200 (GRCm39) |
D1611E |
possibly damaging |
Het |
Mroh2a |
G |
A |
1: 88,171,805 (GRCm39) |
|
probably null |
Het |
Nek5 |
A |
G |
8: 22,603,688 (GRCm39) |
V138A |
probably damaging |
Het |
Opcml |
A |
T |
9: 28,813,463 (GRCm39) |
E251D |
probably benign |
Het |
Or13c7e-ps1 |
T |
A |
4: 43,782,175 (GRCm39) |
I52F |
probably benign |
Het |
Or1j14 |
T |
A |
2: 36,418,176 (GRCm39) |
Y251N |
probably damaging |
Het |
Or1o1 |
A |
T |
17: 37,717,260 (GRCm39) |
M274L |
probably benign |
Het |
Pde1b |
A |
T |
15: 103,411,901 (GRCm39) |
M1L |
probably benign |
Het |
Pias1 |
G |
A |
9: 62,859,266 (GRCm39) |
H72Y |
probably damaging |
Het |
Postn |
G |
A |
3: 54,277,679 (GRCm39) |
V225I |
probably damaging |
Het |
Prickle2 |
A |
G |
6: 92,353,483 (GRCm39) |
V661A |
probably benign |
Het |
Ptpn1 |
T |
A |
2: 167,816,161 (GRCm39) |
F225Y |
probably damaging |
Het |
Ptprd |
C |
T |
4: 75,868,898 (GRCm39) |
V1425M |
probably damaging |
Het |
Rbfox1 |
C |
A |
16: 7,094,954 (GRCm39) |
S111R |
probably benign |
Het |
Rbm24 |
T |
C |
13: 46,572,676 (GRCm39) |
|
probably null |
Het |
Rlf |
T |
G |
4: 121,027,954 (GRCm39) |
K224T |
probably damaging |
Het |
Sdr42e2 |
T |
C |
7: 120,419,873 (GRCm39) |
L206P |
probably damaging |
Het |
Serpinb9g |
A |
G |
13: 33,676,854 (GRCm39) |
E212G |
probably damaging |
Het |
Sh3pxd2a |
T |
C |
19: 47,257,146 (GRCm39) |
Y524C |
probably damaging |
Het |
Sh3pxd2a |
C |
A |
19: 47,258,277 (GRCm39) |
E475D |
probably null |
Het |
Skil |
A |
G |
3: 31,151,603 (GRCm39) |
T42A |
probably benign |
Het |
Sorcs2 |
A |
G |
5: 36,311,207 (GRCm39) |
V203A |
probably damaging |
Het |
Sugp2 |
C |
T |
8: 70,695,641 (GRCm39) |
R205* |
probably null |
Het |
Tle1 |
C |
A |
4: 72,057,203 (GRCm39) |
|
probably benign |
Het |
Tmem63c |
T |
A |
12: 87,119,660 (GRCm39) |
L318Q |
probably damaging |
Het |
Txnrd1 |
A |
G |
10: 82,717,759 (GRCm39) |
I248V |
probably benign |
Het |
Vmn2r79 |
T |
A |
7: 86,686,741 (GRCm39) |
C707* |
probably null |
Het |
Xdh |
C |
T |
17: 74,241,837 (GRCm39) |
G154D |
probably damaging |
Het |
Xirp2 |
T |
A |
2: 67,355,713 (GRCm39) |
D3491E |
probably benign |
Het |
Yjefn3 |
A |
G |
8: 70,341,869 (GRCm39) |
L77P |
probably damaging |
Het |
Zer1 |
C |
T |
2: 29,991,862 (GRCm39) |
E653K |
probably damaging |
Het |
Zfyve27 |
T |
C |
19: 42,167,911 (GRCm39) |
V151A |
probably benign |
Het |
Zim1 |
T |
A |
7: 6,685,064 (GRCm39) |
S129C |
probably damaging |
Het |
|
Other mutations in Scgb2b3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1664:Scgb2b3
|
UTSW |
7 |
31,058,464 (GRCm39) |
makesense |
probably null |
|
R1772:Scgb2b3
|
UTSW |
7 |
31,059,621 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3862:Scgb2b3
|
UTSW |
7 |
31,061,430 (GRCm39) |
critical splice donor site |
probably null |
|
R5819:Scgb2b3
|
UTSW |
7 |
31,059,639 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6433:Scgb2b3
|
UTSW |
7 |
31,058,492 (GRCm39) |
missense |
probably benign |
0.15 |
R7135:Scgb2b3
|
UTSW |
7 |
31,059,639 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7145:Scgb2b3
|
UTSW |
7 |
31,059,573 (GRCm39) |
missense |
probably benign |
0.00 |
R7553:Scgb2b3
|
UTSW |
7 |
31,059,673 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7908:Scgb2b3
|
UTSW |
7 |
31,061,439 (GRCm39) |
missense |
probably damaging |
0.98 |
R8172:Scgb2b3
|
UTSW |
7 |
31,058,476 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9276:Scgb2b3
|
UTSW |
7 |
31,059,528 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9371:Scgb2b3
|
UTSW |
7 |
31,059,642 (GRCm39) |
missense |
probably benign |
0.04 |
X0027:Scgb2b3
|
UTSW |
7 |
31,059,681 (GRCm39) |
missense |
probably benign |
0.00 |
Z1186:Scgb2b3
|
UTSW |
7 |
31,059,592 (GRCm39) |
missense |
probably benign |
|
Z1186:Scgb2b3
|
UTSW |
7 |
31,058,546 (GRCm39) |
missense |
probably benign |
|
|