Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ada |
A |
G |
2: 163,573,053 (GRCm39) |
L193P |
probably benign |
Het |
Ago2 |
A |
T |
15: 72,995,314 (GRCm39) |
|
probably benign |
Het |
Ankrd26 |
A |
G |
6: 118,500,511 (GRCm39) |
S987P |
probably damaging |
Het |
Ap2a2 |
T |
C |
7: 141,211,277 (GRCm39) |
F938L |
possibly damaging |
Het |
Arhgap35 |
A |
G |
7: 16,296,803 (GRCm39) |
V754A |
possibly damaging |
Het |
Atp10b |
A |
T |
11: 43,088,336 (GRCm39) |
N314I |
probably damaging |
Het |
Atp5f1a |
T |
C |
18: 77,867,849 (GRCm39) |
V291A |
probably damaging |
Het |
Ccm2 |
C |
A |
11: 6,534,544 (GRCm39) |
P19T |
probably damaging |
Het |
Cdc5l |
C |
A |
17: 45,715,573 (GRCm39) |
A680S |
probably benign |
Het |
Cds1 |
A |
G |
5: 101,960,376 (GRCm39) |
T276A |
probably damaging |
Het |
Cit |
A |
G |
5: 116,144,058 (GRCm39) |
R1976G |
possibly damaging |
Het |
Col6a5 |
T |
C |
9: 105,803,020 (GRCm39) |
D1315G |
unknown |
Het |
Emilin1 |
T |
G |
5: 31,078,007 (GRCm39) |
L922R |
probably damaging |
Het |
Fank1 |
T |
C |
7: 133,478,578 (GRCm39) |
L213P |
probably damaging |
Het |
Foxc2 |
T |
C |
8: 121,844,788 (GRCm39) |
S479P |
probably benign |
Het |
Golgb1 |
G |
A |
16: 36,732,442 (GRCm39) |
R563H |
possibly damaging |
Het |
Hoxb13 |
A |
G |
11: 96,085,669 (GRCm39) |
Y134C |
probably damaging |
Het |
Krtap4-16 |
A |
T |
11: 99,742,167 (GRCm39) |
C78S |
possibly damaging |
Het |
Lars1 |
C |
T |
18: 42,347,824 (GRCm39) |
|
probably null |
Het |
Lipe |
T |
C |
7: 25,083,057 (GRCm39) |
N740S |
probably damaging |
Het |
Mbd1 |
C |
T |
18: 74,408,498 (GRCm39) |
|
probably benign |
Het |
Mbd5 |
A |
G |
2: 49,203,721 (GRCm39) |
D1700G |
probably damaging |
Het |
Mpp7 |
A |
G |
18: 7,403,297 (GRCm39) |
Y338H |
probably damaging |
Het |
Pdgfrl |
A |
G |
8: 41,438,631 (GRCm39) |
D189G |
probably damaging |
Het |
Pira12 |
T |
C |
7: 3,900,239 (GRCm39) |
Y121C |
probably damaging |
Het |
Ppm1e |
C |
A |
11: 87,131,488 (GRCm39) |
A302S |
probably damaging |
Het |
Rassf8 |
A |
G |
6: 145,762,916 (GRCm39) |
|
probably benign |
Het |
Rttn |
T |
C |
18: 88,990,618 (GRCm39) |
W52R |
probably damaging |
Het |
Skint8 |
T |
C |
4: 111,796,790 (GRCm39) |
V298A |
probably benign |
Het |
Tulp1 |
A |
T |
17: 28,577,516 (GRCm39) |
|
probably benign |
Het |
Unc5c |
T |
A |
3: 141,494,651 (GRCm39) |
D321E |
probably benign |
Het |
Usp16 |
G |
A |
16: 87,276,627 (GRCm39) |
C654Y |
probably damaging |
Het |
Vwce |
G |
A |
19: 10,632,764 (GRCm39) |
W575* |
probably null |
Het |
Wdr89 |
T |
G |
12: 75,679,873 (GRCm39) |
D127A |
probably damaging |
Het |
Zc3h6 |
G |
A |
2: 128,839,715 (GRCm39) |
R176Q |
probably damaging |
Het |
Zfp942 |
A |
G |
17: 22,151,972 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Plxnc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00843:Plxnc1
|
APN |
10 |
94,683,411 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01285:Plxnc1
|
APN |
10 |
94,635,230 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01867:Plxnc1
|
APN |
10 |
94,634,008 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01994:Plxnc1
|
APN |
10 |
94,685,801 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02083:Plxnc1
|
APN |
10 |
94,758,587 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02250:Plxnc1
|
APN |
10 |
94,706,893 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02429:Plxnc1
|
APN |
10 |
94,718,453 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02752:Plxnc1
|
APN |
10 |
94,630,542 (GRCm39) |
splice site |
probably null |
|
R0230:Plxnc1
|
UTSW |
10 |
94,635,209 (GRCm39) |
missense |
probably benign |
0.07 |
R0265:Plxnc1
|
UTSW |
10 |
94,648,991 (GRCm39) |
missense |
probably benign |
0.14 |
R0271:Plxnc1
|
UTSW |
10 |
94,673,780 (GRCm39) |
missense |
probably null |
1.00 |
R0299:Plxnc1
|
UTSW |
10 |
94,685,683 (GRCm39) |
critical splice donor site |
probably null |
|
R0361:Plxnc1
|
UTSW |
10 |
94,700,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R0441:Plxnc1
|
UTSW |
10 |
94,632,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R0558:Plxnc1
|
UTSW |
10 |
94,673,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Plxnc1
|
UTSW |
10 |
94,635,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Plxnc1
|
UTSW |
10 |
94,635,194 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0692:Plxnc1
|
UTSW |
10 |
94,673,362 (GRCm39) |
critical splice donor site |
probably null |
|
R0751:Plxnc1
|
UTSW |
10 |
94,667,195 (GRCm39) |
splice site |
probably benign |
|
R1184:Plxnc1
|
UTSW |
10 |
94,667,195 (GRCm39) |
splice site |
probably benign |
|
R1260:Plxnc1
|
UTSW |
10 |
94,667,227 (GRCm39) |
missense |
probably damaging |
0.99 |
R1680:Plxnc1
|
UTSW |
10 |
94,677,413 (GRCm39) |
missense |
probably benign |
0.14 |
R1746:Plxnc1
|
UTSW |
10 |
94,680,041 (GRCm39) |
splice site |
probably null |
|
R1750:Plxnc1
|
UTSW |
10 |
94,635,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Plxnc1
|
UTSW |
10 |
94,685,677 (GRCm39) |
unclassified |
probably benign |
|
R1768:Plxnc1
|
UTSW |
10 |
94,680,184 (GRCm39) |
missense |
probably benign |
0.05 |
R1876:Plxnc1
|
UTSW |
10 |
94,702,803 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2004:Plxnc1
|
UTSW |
10 |
94,688,484 (GRCm39) |
missense |
probably damaging |
0.98 |
R2031:Plxnc1
|
UTSW |
10 |
94,779,529 (GRCm39) |
missense |
probably benign |
0.26 |
R2184:Plxnc1
|
UTSW |
10 |
94,780,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R2437:Plxnc1
|
UTSW |
10 |
94,742,395 (GRCm39) |
missense |
probably benign |
0.02 |
R2927:Plxnc1
|
UTSW |
10 |
94,629,154 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3001:Plxnc1
|
UTSW |
10 |
94,629,080 (GRCm39) |
missense |
probably damaging |
0.98 |
R3002:Plxnc1
|
UTSW |
10 |
94,629,080 (GRCm39) |
missense |
probably damaging |
0.98 |
R3003:Plxnc1
|
UTSW |
10 |
94,629,080 (GRCm39) |
missense |
probably damaging |
0.98 |
R3441:Plxnc1
|
UTSW |
10 |
94,706,872 (GRCm39) |
missense |
probably benign |
0.00 |
R3849:Plxnc1
|
UTSW |
10 |
94,630,294 (GRCm39) |
missense |
probably benign |
0.01 |
R3884:Plxnc1
|
UTSW |
10 |
94,746,549 (GRCm39) |
splice site |
probably null |
|
R4004:Plxnc1
|
UTSW |
10 |
94,630,459 (GRCm39) |
nonsense |
probably null |
|
R4679:Plxnc1
|
UTSW |
10 |
94,630,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R4730:Plxnc1
|
UTSW |
10 |
94,703,330 (GRCm39) |
intron |
probably benign |
|
R4937:Plxnc1
|
UTSW |
10 |
94,677,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Plxnc1
|
UTSW |
10 |
94,635,239 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5345:Plxnc1
|
UTSW |
10 |
94,685,831 (GRCm39) |
missense |
probably benign |
0.26 |
R5397:Plxnc1
|
UTSW |
10 |
94,679,614 (GRCm39) |
missense |
probably benign |
0.08 |
R5416:Plxnc1
|
UTSW |
10 |
94,673,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R5485:Plxnc1
|
UTSW |
10 |
94,758,604 (GRCm39) |
missense |
probably benign |
0.00 |
R5543:Plxnc1
|
UTSW |
10 |
94,700,636 (GRCm39) |
missense |
probably benign |
|
R5826:Plxnc1
|
UTSW |
10 |
94,635,335 (GRCm39) |
critical splice donor site |
probably null |
|
R6007:Plxnc1
|
UTSW |
10 |
94,629,152 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6018:Plxnc1
|
UTSW |
10 |
94,779,710 (GRCm39) |
missense |
probably benign |
0.21 |
R6052:Plxnc1
|
UTSW |
10 |
94,779,635 (GRCm39) |
missense |
probably benign |
0.13 |
R6291:Plxnc1
|
UTSW |
10 |
94,669,504 (GRCm39) |
splice site |
probably null |
|
R6653:Plxnc1
|
UTSW |
10 |
94,779,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R6984:Plxnc1
|
UTSW |
10 |
94,667,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7086:Plxnc1
|
UTSW |
10 |
94,667,297 (GRCm39) |
missense |
probably benign |
|
R7401:Plxnc1
|
UTSW |
10 |
94,706,867 (GRCm39) |
missense |
probably benign |
|
R7727:Plxnc1
|
UTSW |
10 |
94,779,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R7789:Plxnc1
|
UTSW |
10 |
94,630,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R7803:Plxnc1
|
UTSW |
10 |
94,779,377 (GRCm39) |
critical splice donor site |
probably null |
|
R7809:Plxnc1
|
UTSW |
10 |
94,630,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7882:Plxnc1
|
UTSW |
10 |
94,679,698 (GRCm39) |
missense |
probably benign |
|
R8103:Plxnc1
|
UTSW |
10 |
94,706,944 (GRCm39) |
missense |
probably benign |
|
R8226:Plxnc1
|
UTSW |
10 |
94,669,230 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8273:Plxnc1
|
UTSW |
10 |
94,649,105 (GRCm39) |
missense |
probably benign |
0.14 |
R8299:Plxnc1
|
UTSW |
10 |
94,663,041 (GRCm39) |
missense |
probably benign |
0.35 |
R8392:Plxnc1
|
UTSW |
10 |
94,637,352 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8758:Plxnc1
|
UTSW |
10 |
94,758,607 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8806:Plxnc1
|
UTSW |
10 |
94,635,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R8882:Plxnc1
|
UTSW |
10 |
94,677,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R8893:Plxnc1
|
UTSW |
10 |
94,685,709 (GRCm39) |
missense |
probably benign |
0.35 |
R8956:Plxnc1
|
UTSW |
10 |
94,746,448 (GRCm39) |
missense |
probably benign |
0.00 |
R9040:Plxnc1
|
UTSW |
10 |
94,779,379 (GRCm39) |
nonsense |
probably null |
|
R9102:Plxnc1
|
UTSW |
10 |
94,663,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R9225:Plxnc1
|
UTSW |
10 |
94,629,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R9324:Plxnc1
|
UTSW |
10 |
94,780,685 (GRCm39) |
start gained |
probably benign |
|
R9368:Plxnc1
|
UTSW |
10 |
94,700,599 (GRCm39) |
nonsense |
probably null |
|
R9375:Plxnc1
|
UTSW |
10 |
94,649,093 (GRCm39) |
missense |
probably benign |
0.20 |
R9430:Plxnc1
|
UTSW |
10 |
94,758,544 (GRCm39) |
missense |
probably benign |
0.01 |
R9460:Plxnc1
|
UTSW |
10 |
94,700,895 (GRCm39) |
missense |
probably benign |
|
R9498:Plxnc1
|
UTSW |
10 |
94,649,004 (GRCm39) |
missense |
possibly damaging |
0.48 |
RF003:Plxnc1
|
UTSW |
10 |
94,630,306 (GRCm39) |
missense |
probably damaging |
1.00 |
RF045:Plxnc1
|
UTSW |
10 |
94,700,869 (GRCm39) |
missense |
probably damaging |
1.00 |
RF046:Plxnc1
|
UTSW |
10 |
94,700,869 (GRCm39) |
missense |
probably damaging |
1.00 |
RF047:Plxnc1
|
UTSW |
10 |
94,700,869 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:Plxnc1
|
UTSW |
10 |
94,700,577 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Plxnc1
|
UTSW |
10 |
94,700,891 (GRCm39) |
missense |
probably benign |
0.16 |
|