Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abr |
A |
G |
11: 76,355,108 (GRCm39) |
Y249H |
probably damaging |
Het |
Afdn |
T |
A |
17: 14,024,270 (GRCm39) |
C59S |
probably damaging |
Het |
Akap11 |
C |
A |
14: 78,751,149 (GRCm39) |
V413F |
|
Het |
Ank3 |
T |
C |
10: 69,822,662 (GRCm39) |
S444P |
probably damaging |
Het |
Ankrd12 |
C |
T |
17: 66,344,599 (GRCm39) |
E91K |
possibly damaging |
Het |
Arhgap10 |
A |
G |
8: 78,137,665 (GRCm39) |
S309P |
probably damaging |
Het |
Arpc2 |
C |
A |
1: 74,276,041 (GRCm39) |
F19L |
probably benign |
Het |
Atp5f1a |
C |
T |
18: 77,868,997 (GRCm39) |
T457I |
probably damaging |
Het |
Bsn |
C |
T |
9: 107,988,819 (GRCm39) |
R2311H |
probably damaging |
Het |
C1ra |
A |
G |
6: 124,494,383 (GRCm39) |
T277A |
probably benign |
Het |
Celsr3 |
C |
G |
9: 108,715,689 (GRCm39) |
L2124V |
probably benign |
Het |
Cenpv |
T |
C |
11: 62,415,989 (GRCm39) |
*253W |
probably null |
Het |
Cfap54 |
A |
T |
10: 92,875,048 (GRCm39) |
V479E |
possibly damaging |
Het |
Clec1a |
T |
C |
6: 129,428,564 (GRCm39) |
|
probably benign |
Het |
Cmpk2 |
A |
T |
12: 26,519,568 (GRCm39) |
Y73F |
probably benign |
Het |
Cpne2 |
T |
C |
8: 95,281,643 (GRCm39) |
I226T |
possibly damaging |
Het |
Cyp2c67 |
C |
T |
19: 39,597,699 (GRCm39) |
R433Q |
probably damaging |
Het |
Dagla |
A |
G |
19: 10,232,220 (GRCm39) |
Y489H |
probably damaging |
Het |
Dennd4a |
C |
A |
9: 64,749,906 (GRCm39) |
P166T |
probably damaging |
Het |
Dnm2 |
C |
T |
9: 21,416,977 (GRCm39) |
R837W |
possibly damaging |
Het |
Enpp2 |
C |
T |
15: 54,713,484 (GRCm39) |
R658Q |
probably benign |
Het |
Gm10521 |
G |
A |
1: 171,724,030 (GRCm39) |
V114I |
unknown |
Het |
H2-T24 |
T |
A |
17: 36,328,276 (GRCm39) |
E69V |
probably damaging |
Het |
H6pd |
T |
A |
4: 150,080,307 (GRCm39) |
K179N |
probably damaging |
Het |
Hsf2bp |
C |
T |
17: 32,206,336 (GRCm39) |
W265* |
probably null |
Het |
Igfn1 |
C |
A |
1: 135,901,185 (GRCm39) |
R431L |
probably damaging |
Het |
Kcng2 |
T |
C |
18: 80,339,074 (GRCm39) |
S405G |
possibly damaging |
Het |
Leng9 |
T |
C |
7: 4,151,447 (GRCm39) |
T410A |
probably benign |
Het |
Lrp1b |
T |
C |
2: 40,487,076 (GRCm39) |
Y4557C |
|
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Mlkl |
A |
G |
8: 112,043,055 (GRCm39) |
V364A |
probably benign |
Het |
Mns1 |
T |
A |
9: 72,356,507 (GRCm39) |
F254Y |
probably benign |
Het |
Naip1 |
T |
A |
13: 100,562,684 (GRCm39) |
N827I |
probably damaging |
Het |
Neb |
C |
T |
2: 52,146,190 (GRCm39) |
R2929H |
probably damaging |
Het |
Or5m13 |
A |
G |
2: 85,749,046 (GRCm39) |
Y259C |
probably benign |
Het |
Or5v1b |
T |
A |
17: 37,841,819 (GRCm39) |
M317K |
probably benign |
Het |
Pde10a |
A |
G |
17: 9,200,488 (GRCm39) |
*797W |
probably null |
Het |
Pirb |
T |
G |
7: 3,719,859 (GRCm39) |
H429P |
probably benign |
Het |
Plbd1 |
A |
G |
6: 136,594,286 (GRCm39) |
L321P |
probably damaging |
Het |
Pmfbp1 |
A |
G |
8: 110,262,471 (GRCm39) |
I722V |
probably benign |
Het |
Polr2b |
A |
G |
5: 77,471,485 (GRCm39) |
R274G |
probably damaging |
Het |
Prune2 |
C |
T |
19: 17,101,144 (GRCm39) |
T2216I |
probably benign |
Het |
Psma3 |
A |
T |
12: 71,041,156 (GRCm39) |
D252V |
probably benign |
Het |
Ptpn1 |
C |
T |
2: 167,816,176 (GRCm39) |
T230I |
probably damaging |
Het |
Rhpn1 |
T |
C |
15: 75,585,120 (GRCm39) |
V519A |
possibly damaging |
Het |
Rnf213 |
T |
C |
11: 119,326,768 (GRCm39) |
V1586A |
|
Het |
Rrp36 |
T |
A |
17: 46,983,306 (GRCm39) |
K103* |
probably null |
Het |
Ryr2 |
T |
C |
13: 11,897,976 (GRCm39) |
T140A |
probably benign |
Het |
Scn1a |
T |
A |
2: 66,130,026 (GRCm39) |
Y243F |
probably damaging |
Het |
Sdk1 |
A |
G |
5: 141,941,953 (GRCm39) |
T534A |
possibly damaging |
Het |
Slc27a5 |
T |
C |
7: 12,731,640 (GRCm39) |
D117G |
probably damaging |
Het |
Slc2a1 |
A |
T |
4: 118,990,607 (GRCm39) |
E246D |
probably benign |
Het |
Smpd2 |
T |
C |
10: 41,363,685 (GRCm39) |
D289G |
probably benign |
Het |
Spag6 |
A |
C |
2: 18,703,985 (GRCm39) |
E11A |
probably benign |
Het |
Stard3 |
G |
A |
11: 98,262,931 (GRCm39) |
|
probably benign |
Het |
Tcf19 |
A |
G |
17: 35,825,899 (GRCm39) |
V86A |
probably damaging |
Het |
Tcstv7a |
T |
C |
13: 120,289,993 (GRCm39) |
S68G |
possibly damaging |
Het |
Tigit |
A |
T |
16: 43,479,833 (GRCm39) |
M154K |
probably benign |
Het |
Trim34a |
T |
A |
7: 103,910,201 (GRCm39) |
N334K |
probably damaging |
Het |
Tsen15 |
T |
C |
1: 152,259,098 (GRCm39) |
I87V |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,738,218 (GRCm39) |
M4153K |
unknown |
Het |
Uchl3 |
A |
T |
14: 101,905,963 (GRCm39) |
|
probably null |
Het |
Usp1 |
A |
G |
4: 98,819,578 (GRCm39) |
K347E |
probably damaging |
Het |
Vmn1r73 |
T |
C |
7: 11,490,479 (GRCm39) |
M99T |
probably benign |
Het |
Vmn2r20 |
A |
G |
6: 123,362,394 (GRCm39) |
W797R |
probably damaging |
Het |
Vwa7 |
A |
G |
17: 35,238,712 (GRCm39) |
T267A |
probably damaging |
Het |
|
Other mutations in Zpld2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02183:Zpld2
|
APN |
4 |
133,929,291 (GRCm39) |
missense |
probably benign |
0.27 |
IGL03170:Zpld2
|
APN |
4 |
133,920,345 (GRCm39) |
missense |
possibly damaging |
0.57 |
FR4342:Zpld2
|
UTSW |
4 |
133,929,942 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Zpld2
|
UTSW |
4 |
133,929,941 (GRCm39) |
small insertion |
probably benign |
|
R0487:Zpld2
|
UTSW |
4 |
133,930,089 (GRCm39) |
missense |
probably damaging |
0.97 |
R0530:Zpld2
|
UTSW |
4 |
133,930,221 (GRCm39) |
missense |
probably benign |
|
R0553:Zpld2
|
UTSW |
4 |
133,929,829 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1121:Zpld2
|
UTSW |
4 |
133,930,248 (GRCm39) |
missense |
probably benign |
0.00 |
R1458:Zpld2
|
UTSW |
4 |
133,924,144 (GRCm39) |
missense |
probably benign |
0.01 |
R1748:Zpld2
|
UTSW |
4 |
133,929,430 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1748:Zpld2
|
UTSW |
4 |
133,927,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R1913:Zpld2
|
UTSW |
4 |
133,919,986 (GRCm39) |
critical splice donor site |
probably null |
|
R2029:Zpld2
|
UTSW |
4 |
133,929,669 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2069:Zpld2
|
UTSW |
4 |
133,929,252 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2237:Zpld2
|
UTSW |
4 |
133,929,516 (GRCm39) |
missense |
unknown |
|
R2239:Zpld2
|
UTSW |
4 |
133,929,516 (GRCm39) |
missense |
unknown |
|
R3943:Zpld2
|
UTSW |
4 |
133,927,656 (GRCm39) |
missense |
probably benign |
0.15 |
R4646:Zpld2
|
UTSW |
4 |
133,929,459 (GRCm39) |
missense |
probably benign |
0.00 |
R4673:Zpld2
|
UTSW |
4 |
133,927,658 (GRCm39) |
missense |
probably benign |
0.01 |
R4838:Zpld2
|
UTSW |
4 |
133,920,410 (GRCm39) |
missense |
probably benign |
0.04 |
R5002:Zpld2
|
UTSW |
4 |
133,924,231 (GRCm39) |
missense |
probably benign |
0.09 |
R5593:Zpld2
|
UTSW |
4 |
133,920,350 (GRCm39) |
missense |
probably damaging |
0.99 |
R5606:Zpld2
|
UTSW |
4 |
133,927,523 (GRCm39) |
missense |
probably benign |
0.13 |
R6553:Zpld2
|
UTSW |
4 |
133,929,367 (GRCm39) |
missense |
probably damaging |
0.99 |
R6834:Zpld2
|
UTSW |
4 |
133,920,476 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6931:Zpld2
|
UTSW |
4 |
133,920,464 (GRCm39) |
missense |
probably benign |
0.28 |
R7526:Zpld2
|
UTSW |
4 |
133,927,384 (GRCm39) |
splice site |
probably null |
|
R7771:Zpld2
|
UTSW |
4 |
133,922,754 (GRCm39) |
missense |
probably benign |
0.01 |
R8271:Zpld2
|
UTSW |
4 |
133,930,278 (GRCm39) |
missense |
unknown |
|
R8725:Zpld2
|
UTSW |
4 |
133,930,150 (GRCm39) |
missense |
probably benign |
0.19 |
R8727:Zpld2
|
UTSW |
4 |
133,930,150 (GRCm39) |
missense |
probably benign |
0.19 |
R8757:Zpld2
|
UTSW |
4 |
133,930,282 (GRCm39) |
missense |
unknown |
|
R8966:Zpld2
|
UTSW |
4 |
133,929,712 (GRCm39) |
missense |
probably damaging |
0.98 |
R8992:Zpld2
|
UTSW |
4 |
133,929,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R9039:Zpld2
|
UTSW |
4 |
133,922,858 (GRCm39) |
missense |
probably damaging |
0.98 |
R9278:Zpld2
|
UTSW |
4 |
133,922,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R9434:Zpld2
|
UTSW |
4 |
133,929,553 (GRCm39) |
missense |
probably benign |
0.01 |
R9458:Zpld2
|
UTSW |
4 |
133,929,312 (GRCm39) |
missense |
probably benign |
0.36 |
R9460:Zpld2
|
UTSW |
4 |
133,929,312 (GRCm39) |
missense |
probably benign |
0.36 |
R9461:Zpld2
|
UTSW |
4 |
133,929,312 (GRCm39) |
missense |
probably benign |
0.36 |
R9480:Zpld2
|
UTSW |
4 |
133,929,312 (GRCm39) |
missense |
probably benign |
0.36 |
R9481:Zpld2
|
UTSW |
4 |
133,929,312 (GRCm39) |
missense |
probably benign |
0.36 |
R9551:Zpld2
|
UTSW |
4 |
133,929,312 (GRCm39) |
missense |
probably benign |
0.36 |
R9552:Zpld2
|
UTSW |
4 |
133,929,312 (GRCm39) |
missense |
probably benign |
0.36 |
R9553:Zpld2
|
UTSW |
4 |
133,929,312 (GRCm39) |
missense |
probably benign |
0.36 |
RF015:Zpld2
|
UTSW |
4 |
133,920,338 (GRCm39) |
missense |
probably benign |
|
T0975:Zpld2
|
UTSW |
4 |
133,929,940 (GRCm39) |
small insertion |
probably benign |
|
Z1176:Zpld2
|
UTSW |
4 |
133,929,988 (GRCm39) |
missense |
probably benign |
|
Z1176:Zpld2
|
UTSW |
4 |
133,927,649 (GRCm39) |
missense |
possibly damaging |
0.90 |
|