Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
T |
G |
7: 119,945,229 (GRCm39) |
L435R |
probably benign |
Het |
Abcc2 |
T |
A |
19: 43,800,941 (GRCm39) |
H627Q |
probably benign |
Het |
Ankhd1 |
A |
T |
18: 36,733,836 (GRCm39) |
|
probably null |
Het |
Ankrd50 |
T |
A |
3: 38,511,510 (GRCm39) |
I286F |
probably damaging |
Het |
Asb15 |
A |
G |
6: 24,562,632 (GRCm39) |
N198S |
probably benign |
Het |
B4galnt2 |
T |
A |
11: 95,782,747 (GRCm39) |
M22L |
probably benign |
Het |
Bcdin3d |
T |
C |
15: 99,368,696 (GRCm39) |
T168A |
probably damaging |
Het |
Bmp1 |
A |
T |
14: 70,728,058 (GRCm39) |
W624R |
probably damaging |
Het |
Cdh4 |
C |
T |
2: 179,422,221 (GRCm39) |
A115V |
probably benign |
Het |
Cfap53 |
A |
G |
18: 74,433,280 (GRCm39) |
T122A |
probably damaging |
Het |
Chsy1 |
A |
G |
7: 65,759,941 (GRCm39) |
K95E |
probably benign |
Het |
Csde1 |
C |
A |
3: 102,960,184 (GRCm39) |
P604T |
probably damaging |
Het |
Cts7 |
A |
T |
13: 61,502,817 (GRCm39) |
L237Q |
probably damaging |
Het |
Cutal |
C |
T |
2: 34,775,933 (GRCm39) |
T88I |
probably benign |
Het |
Dlg4 |
G |
T |
11: 69,914,779 (GRCm39) |
|
probably benign |
Het |
Dnah7c |
C |
A |
1: 46,688,500 (GRCm39) |
T1890K |
probably benign |
Het |
Dnah7c |
A |
G |
1: 46,688,511 (GRCm39) |
S1894G |
probably benign |
Het |
Eif2b4 |
C |
T |
5: 31,349,551 (GRCm39) |
E53K |
possibly damaging |
Het |
Erp44 |
T |
C |
4: 48,205,130 (GRCm39) |
I288V |
probably null |
Het |
Fcamr |
A |
G |
1: 130,740,939 (GRCm39) |
T453A |
possibly damaging |
Het |
Glb1l3 |
T |
C |
9: 26,770,884 (GRCm39) |
T61A |
probably benign |
Het |
Gpr26 |
T |
C |
7: 131,585,830 (GRCm39) |
S267P |
probably benign |
Het |
Heatr6 |
A |
T |
11: 83,650,191 (GRCm39) |
T216S |
probably benign |
Het |
Hephl1 |
C |
T |
9: 14,993,260 (GRCm39) |
V525I |
probably damaging |
Het |
Jak2 |
T |
A |
19: 29,266,110 (GRCm39) |
I517N |
probably benign |
Het |
Kbtbd4 |
T |
A |
2: 90,740,113 (GRCm39) |
Y499* |
probably null |
Het |
Kif1a |
A |
T |
1: 93,005,420 (GRCm39) |
I118N |
probably damaging |
Het |
Klhdc7b |
A |
G |
15: 89,271,292 (GRCm39) |
S725G |
probably benign |
Het |
Mfsd13a |
T |
C |
19: 46,356,305 (GRCm39) |
F137L |
probably damaging |
Het |
Myo7a |
T |
A |
7: 97,703,710 (GRCm39) |
Y1977F |
probably damaging |
Het |
Naip2 |
T |
G |
13: 100,298,352 (GRCm39) |
K561N |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,288,644 (GRCm39) |
V1194I |
probably benign |
Het |
Nkx2-4 |
G |
T |
2: 146,925,860 (GRCm39) |
A334E |
possibly damaging |
Het |
Nlrp9c |
T |
A |
7: 26,070,747 (GRCm39) |
N945Y |
probably damaging |
Het |
Or2z2 |
A |
T |
11: 58,346,394 (GRCm39) |
I127N |
probably damaging |
Het |
Or4e5 |
C |
T |
14: 52,728,250 (GRCm39) |
R57Q |
probably benign |
Het |
Or8g20 |
A |
G |
9: 39,396,048 (GRCm39) |
V164A |
probably benign |
Het |
Pcdha7 |
A |
G |
18: 37,107,539 (GRCm39) |
Q188R |
probably benign |
Het |
Phf3 |
A |
T |
1: 30,844,104 (GRCm39) |
S1618R |
possibly damaging |
Het |
Phip |
C |
A |
9: 82,782,794 (GRCm39) |
E884* |
probably null |
Het |
Qser1 |
A |
G |
2: 104,610,605 (GRCm39) |
V1226A |
possibly damaging |
Het |
Ros1 |
G |
T |
10: 52,018,299 (GRCm39) |
S786R |
probably damaging |
Het |
Rps6ka5 |
A |
G |
12: 100,517,795 (GRCm39) |
S769P |
probably damaging |
Het |
Sfxn3 |
G |
A |
19: 45,038,354 (GRCm39) |
|
probably null |
Het |
Specc1 |
T |
G |
11: 62,037,244 (GRCm39) |
S813A |
probably damaging |
Het |
Spry1 |
T |
C |
3: 37,696,871 (GRCm39) |
I38T |
probably damaging |
Het |
Tagap |
T |
C |
17: 8,152,546 (GRCm39) |
V577A |
probably benign |
Het |
Tmem44 |
T |
C |
16: 30,356,369 (GRCm39) |
D110G |
probably damaging |
Het |
Ubn2 |
A |
G |
6: 38,411,397 (GRCm39) |
E97G |
possibly damaging |
Het |
Ubr4 |
C |
A |
4: 139,200,935 (GRCm39) |
H4706Q |
possibly damaging |
Het |
Usp25 |
T |
A |
16: 76,856,176 (GRCm39) |
N256K |
probably benign |
Het |
Vmn2r112 |
T |
A |
17: 22,820,160 (GRCm39) |
L11Q |
probably null |
Het |
Wnt2b |
C |
A |
3: 104,860,502 (GRCm39) |
R135L |
probably damaging |
Het |
Zfp60 |
T |
C |
7: 27,448,151 (GRCm39) |
F273S |
probably benign |
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 |
|
IGL02973:Plxnc1
|
APN |
10 |
94,646,546 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|
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 |
|