Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310079G19Rik |
C |
A |
16: 88,424,411 (GRCm39) |
V27F |
unknown |
Het |
Akr1c20 |
T |
C |
13: 4,560,222 (GRCm39) |
E152G |
probably damaging |
Het |
Alx4 |
G |
A |
2: 93,473,134 (GRCm39) |
G44D |
possibly damaging |
Het |
Arhgap31 |
T |
A |
16: 38,422,895 (GRCm39) |
E1057V |
possibly damaging |
Het |
Arhgef26 |
A |
T |
3: 62,331,050 (GRCm39) |
D588V |
probably damaging |
Het |
Bag2 |
T |
A |
1: 33,785,997 (GRCm39) |
E108D |
probably benign |
Het |
Ccdc162 |
C |
T |
10: 41,463,375 (GRCm39) |
V183I |
probably benign |
Het |
Ccdc83 |
A |
G |
7: 89,885,563 (GRCm39) |
|
probably benign |
Het |
Ccnyl1 |
G |
A |
1: 64,753,827 (GRCm39) |
E137K |
probably damaging |
Het |
Celsr2 |
T |
C |
3: 108,308,155 (GRCm39) |
T1849A |
probably benign |
Het |
Cep192 |
C |
A |
18: 67,953,400 (GRCm39) |
D472E |
probably benign |
Het |
Cep57l1 |
A |
G |
10: 41,619,110 (GRCm39) |
Y86H |
probably damaging |
Het |
Cep95 |
G |
T |
11: 106,702,112 (GRCm39) |
E370* |
probably null |
Het |
Cldn10 |
A |
G |
14: 119,092,522 (GRCm39) |
T41A |
probably damaging |
Het |
Clptm1l |
T |
A |
13: 73,764,157 (GRCm39) |
Y426N |
probably benign |
Het |
Dipk1b |
T |
C |
2: 26,522,650 (GRCm39) |
L33S |
possibly damaging |
Het |
Eps15 |
T |
C |
4: 109,166,374 (GRCm39) |
V89A |
probably damaging |
Het |
Fam53b |
A |
G |
7: 132,361,654 (GRCm39) |
S125P |
probably damaging |
Het |
Fbxo44 |
A |
T |
4: 148,240,461 (GRCm39) |
W256R |
probably benign |
Het |
Gnl2 |
T |
C |
4: 124,940,067 (GRCm39) |
V313A |
probably damaging |
Het |
Hyal4 |
A |
G |
6: 24,756,513 (GRCm39) |
R244G |
probably damaging |
Het |
Irf6 |
G |
T |
1: 192,844,931 (GRCm39) |
W134L |
probably benign |
Het |
Kcnu1 |
A |
G |
8: 26,371,448 (GRCm39) |
T286A |
probably damaging |
Het |
Lpcat2 |
T |
C |
8: 93,644,798 (GRCm39) |
V529A |
possibly damaging |
Het |
Lrfn2 |
A |
G |
17: 49,378,188 (GRCm39) |
E423G |
possibly damaging |
Het |
Lrp8 |
G |
T |
4: 107,705,499 (GRCm39) |
R209L |
probably benign |
Het |
Mgll |
T |
C |
6: 88,741,570 (GRCm39) |
|
probably benign |
Het |
Mix23 |
T |
C |
16: 35,901,775 (GRCm39) |
|
probably null |
Het |
Mta3 |
A |
G |
17: 84,070,417 (GRCm39) |
I193V |
probably damaging |
Het |
Nedd4l |
G |
A |
18: 65,342,790 (GRCm39) |
V909I |
possibly damaging |
Het |
Or10al5 |
T |
A |
17: 38,063,271 (GRCm39) |
C175* |
probably null |
Het |
Or3a1d |
A |
T |
11: 74,238,023 (GRCm39) |
I129N |
probably damaging |
Het |
Or5p66 |
A |
T |
7: 107,885,663 (GRCm39) |
Y223* |
probably null |
Het |
Or6c206 |
A |
T |
10: 129,097,093 (GRCm39) |
K88* |
probably null |
Het |
Orc1 |
T |
C |
4: 108,461,218 (GRCm39) |
V526A |
probably damaging |
Het |
Pard3b |
T |
C |
1: 62,383,137 (GRCm39) |
S744P |
probably damaging |
Het |
Pcnx3 |
G |
A |
19: 5,733,367 (GRCm39) |
Q155* |
probably null |
Het |
Pcnx3 |
C |
G |
19: 5,733,368 (GRCm39) |
L1F |
probably null |
Het |
Pdcd11 |
T |
A |
19: 47,115,684 (GRCm39) |
|
probably benign |
Het |
Pi4k2a |
G |
A |
19: 42,079,131 (GRCm39) |
R64Q |
probably damaging |
Het |
Pigt |
A |
G |
2: 164,343,565 (GRCm39) |
D347G |
probably benign |
Het |
Rbm27 |
T |
C |
18: 42,425,177 (GRCm39) |
|
probably benign |
Het |
Rpl7a-ps10 |
A |
G |
9: 97,061,926 (GRCm39) |
E232G |
probably damaging |
Het |
Rprd2 |
A |
G |
3: 95,671,872 (GRCm39) |
L1177P |
probably damaging |
Het |
Rrn3 |
T |
A |
16: 13,601,959 (GRCm39) |
L71* |
probably null |
Het |
Sbspon |
A |
G |
1: 15,962,669 (GRCm39) |
C70R |
probably damaging |
Het |
Smtn |
A |
T |
11: 3,482,865 (GRCm39) |
|
probably null |
Het |
Son |
A |
G |
16: 91,453,614 (GRCm39) |
D787G |
probably damaging |
Het |
Sphkap |
C |
T |
1: 83,254,833 (GRCm39) |
S972N |
probably benign |
Het |
Spopl |
C |
T |
2: 23,427,392 (GRCm39) |
R221Q |
probably damaging |
Het |
Srp14 |
A |
C |
2: 118,309,440 (GRCm39) |
L58V |
probably null |
Het |
Sun2 |
A |
G |
15: 79,612,114 (GRCm39) |
S522P |
possibly damaging |
Het |
Tectb |
C |
G |
19: 55,169,431 (GRCm39) |
|
probably benign |
Het |
Trdn |
T |
C |
10: 33,033,162 (GRCm39) |
I129T |
probably benign |
Het |
Trpv3 |
A |
G |
11: 73,169,780 (GRCm39) |
K117R |
probably benign |
Het |
Ubqlnl |
A |
T |
7: 103,798,345 (GRCm39) |
I384N |
probably benign |
Het |
Ush2a |
G |
A |
1: 188,542,489 (GRCm39) |
G3352S |
probably benign |
Het |
Vmn1r59 |
A |
T |
7: 5,457,637 (GRCm39) |
I41K |
probably damaging |
Het |
Vmn2r125 |
T |
A |
4: 156,702,419 (GRCm39) |
Y68* |
probably null |
Het |
|
Other mutations in Zpld1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01360:Zpld1
|
APN |
16 |
55,046,748 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01380:Zpld1
|
APN |
16 |
55,072,133 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02089:Zpld1
|
APN |
16 |
55,071,974 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03350:Zpld1
|
APN |
16 |
55,061,692 (GRCm39) |
splice site |
probably benign |
|
whirl
|
UTSW |
16 |
55,053,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R0324:Zpld1
|
UTSW |
16 |
55,071,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R1296:Zpld1
|
UTSW |
16 |
55,068,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R1500:Zpld1
|
UTSW |
16 |
55,053,935 (GRCm39) |
missense |
probably damaging |
0.97 |
R4096:Zpld1
|
UTSW |
16 |
55,053,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R4835:Zpld1
|
UTSW |
16 |
55,068,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R5153:Zpld1
|
UTSW |
16 |
55,067,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5412:Zpld1
|
UTSW |
16 |
55,052,646 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5527:Zpld1
|
UTSW |
16 |
55,046,725 (GRCm39) |
missense |
probably benign |
0.06 |
R5537:Zpld1
|
UTSW |
16 |
55,054,003 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6167:Zpld1
|
UTSW |
16 |
55,053,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R6178:Zpld1
|
UTSW |
16 |
55,053,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Zpld1
|
UTSW |
16 |
55,052,603 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6877:Zpld1
|
UTSW |
16 |
55,072,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R7165:Zpld1
|
UTSW |
16 |
55,052,594 (GRCm39) |
missense |
probably benign |
0.03 |
R7382:Zpld1
|
UTSW |
16 |
55,067,046 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7423:Zpld1
|
UTSW |
16 |
55,054,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R8217:Zpld1
|
UTSW |
16 |
55,047,295 (GRCm39) |
critical splice donor site |
probably null |
|
R8377:Zpld1
|
UTSW |
16 |
55,067,017 (GRCm39) |
missense |
probably benign |
0.04 |
R9076:Zpld1
|
UTSW |
16 |
55,061,764 (GRCm39) |
missense |
probably benign |
0.32 |
R9564:Zpld1
|
UTSW |
16 |
55,061,701 (GRCm39) |
nonsense |
probably null |
|
Z1176:Zpld1
|
UTSW |
16 |
55,072,128 (GRCm39) |
missense |
probably damaging |
1.00 |
|