Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921511C20Rik |
T |
A |
X: 126,303,196 (GRCm39) |
S378R |
probably benign |
Het |
Abca14 |
T |
A |
7: 119,852,612 (GRCm39) |
M859K |
probably benign |
Het |
Adamts13 |
C |
T |
2: 26,875,495 (GRCm39) |
P462S |
probably damaging |
Het |
Apol7a |
G |
T |
15: 77,277,690 (GRCm39) |
D19E |
possibly damaging |
Het |
Armc8 |
T |
C |
9: 99,366,031 (GRCm39) |
N628D |
possibly damaging |
Het |
Astn2 |
T |
A |
4: 66,184,471 (GRCm39) |
I209F |
unknown |
Het |
Atp10b |
T |
C |
11: 43,085,492 (GRCm39) |
|
probably null |
Het |
C4b |
C |
T |
17: 34,953,465 (GRCm39) |
C1006Y |
probably damaging |
Het |
Capn13 |
A |
G |
17: 73,637,993 (GRCm39) |
L470P |
probably damaging |
Het |
Col4a4 |
T |
C |
1: 82,431,530 (GRCm39) |
R1585G |
unknown |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Csmd3 |
C |
T |
15: 47,449,084 (GRCm39) |
V3637M |
probably damaging |
Het |
Dgki |
C |
T |
6: 36,993,610 (GRCm39) |
D584N |
probably damaging |
Het |
Dmrt2 |
T |
C |
19: 25,655,498 (GRCm39) |
S366P |
probably damaging |
Het |
Dmtf1 |
A |
C |
5: 9,186,070 (GRCm39) |
L172R |
probably damaging |
Het |
Efhc2 |
A |
G |
X: 17,096,817 (GRCm39) |
F177L |
probably damaging |
Het |
Enpep |
T |
A |
3: 129,063,926 (GRCm39) |
|
probably benign |
Het |
Enpp6 |
A |
T |
8: 47,518,967 (GRCm39) |
D245V |
probably damaging |
Het |
Fam199x |
T |
A |
X: 135,963,399 (GRCm39) |
|
probably benign |
Het |
Fkbp4 |
A |
T |
6: 128,411,433 (GRCm39) |
|
probably benign |
Het |
Gas7 |
A |
G |
11: 67,534,158 (GRCm39) |
H86R |
probably benign |
Het |
Gcc2 |
A |
G |
10: 58,107,458 (GRCm39) |
N862S |
probably benign |
Het |
Gstm7 |
T |
C |
3: 107,837,594 (GRCm39) |
D115G |
possibly damaging |
Het |
Gtse1 |
C |
A |
15: 85,746,799 (GRCm39) |
P205Q |
possibly damaging |
Het |
H2bc1 |
A |
T |
13: 24,118,093 (GRCm39) |
F16Y |
probably benign |
Het |
Herc4 |
G |
A |
10: 63,109,345 (GRCm39) |
M193I |
probably benign |
Het |
Igfl3 |
T |
A |
7: 17,913,763 (GRCm39) |
C38S |
possibly damaging |
Het |
Il18rap |
G |
A |
1: 40,587,082 (GRCm39) |
D455N |
probably damaging |
Het |
Ints8 |
A |
G |
4: 11,209,244 (GRCm39) |
I932T |
probably damaging |
Het |
Itgbl1 |
A |
C |
14: 124,209,553 (GRCm39) |
I311L |
probably benign |
Het |
Jmjd1c |
A |
T |
10: 67,056,101 (GRCm39) |
H794L |
probably damaging |
Het |
Kif1a |
A |
G |
1: 92,948,271 (GRCm39) |
S1542P |
probably benign |
Het |
Klc3 |
T |
A |
7: 19,129,750 (GRCm39) |
N373I |
probably damaging |
Het |
Lcn2 |
T |
C |
2: 32,274,877 (GRCm39) |
*201W |
probably null |
Het |
Ldhb |
A |
T |
6: 142,441,292 (GRCm39) |
|
probably null |
Het |
Lyst |
G |
A |
13: 13,835,541 (GRCm39) |
C1741Y |
probably benign |
Het |
Npat |
T |
A |
9: 53,470,417 (GRCm39) |
S348T |
probably benign |
Het |
Pclo |
A |
T |
5: 14,906,999 (GRCm39) |
D5001V |
unknown |
Het |
Peg3 |
C |
A |
7: 6,712,010 (GRCm39) |
A1071S |
probably benign |
Het |
Piwil2 |
A |
T |
14: 70,628,822 (GRCm39) |
D731E |
possibly damaging |
Het |
Prss41 |
T |
A |
17: 24,062,830 (GRCm39) |
D35V |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 22,965,181 (GRCm39) |
D159E |
possibly damaging |
Het |
Rabep1 |
C |
T |
11: 70,814,023 (GRCm39) |
Q571* |
probably null |
Het |
Scn8a |
A |
G |
15: 100,927,453 (GRCm39) |
|
probably null |
Het |
Sipa1l2 |
G |
A |
8: 126,174,576 (GRCm39) |
T1234I |
possibly damaging |
Het |
Slc5a10 |
T |
A |
11: 61,564,738 (GRCm39) |
M414L |
probably benign |
Het |
Smg5 |
T |
C |
3: 88,260,305 (GRCm39) |
S632P |
possibly damaging |
Het |
Smim15 |
A |
G |
13: 108,184,048 (GRCm39) |
D18G |
probably benign |
Het |
Sorl1 |
T |
A |
9: 41,929,478 (GRCm39) |
I1132F |
probably damaging |
Het |
Spatc1 |
T |
C |
15: 76,167,739 (GRCm39) |
|
probably benign |
Het |
Sytl2 |
A |
T |
7: 90,030,422 (GRCm39) |
|
probably benign |
Het |
Tesc |
A |
G |
5: 118,199,683 (GRCm39) |
D195G |
probably damaging |
Het |
Vmn2r52 |
A |
G |
7: 9,905,029 (GRCm39) |
V270A |
probably damaging |
Het |
Wdr3 |
C |
A |
3: 100,054,016 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Tmem39b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02423:Tmem39b
|
APN |
4 |
129,572,442 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4514001:Tmem39b
|
UTSW |
4 |
129,578,290 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0502:Tmem39b
|
UTSW |
4 |
129,580,779 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0503:Tmem39b
|
UTSW |
4 |
129,580,779 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1483:Tmem39b
|
UTSW |
4 |
129,570,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:Tmem39b
|
UTSW |
4 |
129,578,275 (GRCm39) |
missense |
probably benign |
0.30 |
R1612:Tmem39b
|
UTSW |
4 |
129,580,715 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1751:Tmem39b
|
UTSW |
4 |
129,586,976 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1767:Tmem39b
|
UTSW |
4 |
129,586,976 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1771:Tmem39b
|
UTSW |
4 |
129,587,011 (GRCm39) |
missense |
probably damaging |
0.99 |
R2140:Tmem39b
|
UTSW |
4 |
129,572,481 (GRCm39) |
missense |
probably benign |
0.30 |
R2202:Tmem39b
|
UTSW |
4 |
129,587,716 (GRCm39) |
missense |
probably benign |
0.03 |
R2204:Tmem39b
|
UTSW |
4 |
129,587,716 (GRCm39) |
missense |
probably benign |
0.03 |
R2205:Tmem39b
|
UTSW |
4 |
129,587,716 (GRCm39) |
missense |
probably benign |
0.03 |
R6176:Tmem39b
|
UTSW |
4 |
129,586,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Tmem39b
|
UTSW |
4 |
129,580,584 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6551:Tmem39b
|
UTSW |
4 |
129,585,896 (GRCm39) |
missense |
probably benign |
|
R6654:Tmem39b
|
UTSW |
4 |
129,580,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R6934:Tmem39b
|
UTSW |
4 |
129,572,366 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6988:Tmem39b
|
UTSW |
4 |
129,586,941 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7614:Tmem39b
|
UTSW |
4 |
129,587,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:Tmem39b
|
UTSW |
4 |
129,572,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R8708:Tmem39b
|
UTSW |
4 |
129,570,191 (GRCm39) |
unclassified |
probably benign |
|
R9249:Tmem39b
|
UTSW |
4 |
129,572,468 (GRCm39) |
missense |
probably damaging |
0.99 |
X0024:Tmem39b
|
UTSW |
4 |
129,578,240 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1088:Tmem39b
|
UTSW |
4 |
129,586,270 (GRCm39) |
missense |
probably benign |
0.03 |
|