Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110025L11Rik |
T |
C |
16: 88,860,873 (GRCm39) |
|
probably benign |
Het |
Abcc4 |
A |
G |
14: 118,865,103 (GRCm39) |
S308P |
probably damaging |
Het |
Agr3 |
G |
T |
12: 35,997,832 (GRCm39) |
V115L |
probably damaging |
Het |
Ahr |
A |
T |
12: 35,557,463 (GRCm39) |
I319N |
probably damaging |
Het |
Alpk1 |
A |
T |
3: 127,473,507 (GRCm39) |
V832D |
probably damaging |
Het |
Ano1 |
T |
C |
7: 144,223,289 (GRCm39) |
T78A |
probably benign |
Het |
Apob |
G |
A |
12: 8,045,585 (GRCm39) |
G897D |
probably damaging |
Het |
Arfgef1 |
A |
G |
1: 10,212,891 (GRCm39) |
F1677L |
probably benign |
Het |
Arhgap40 |
G |
T |
2: 158,374,226 (GRCm39) |
G217W |
probably benign |
Het |
Arhgef4 |
A |
G |
1: 34,761,749 (GRCm39) |
E335G |
unknown |
Het |
Calcoco2 |
T |
C |
11: 95,994,374 (GRCm39) |
T60A |
probably damaging |
Het |
Catsperg1 |
A |
T |
7: 28,889,721 (GRCm39) |
S741T |
probably benign |
Het |
Ccdc181 |
T |
G |
1: 164,105,846 (GRCm39) |
I27S |
probably damaging |
Het |
Ceacam9 |
A |
T |
7: 16,459,334 (GRCm39) |
Y211F |
probably damaging |
Het |
Cep41 |
T |
C |
6: 30,671,318 (GRCm39) |
|
probably null |
Het |
Cercam |
T |
A |
2: 29,759,689 (GRCm39) |
L45Q |
probably damaging |
Het |
Cnnm2 |
G |
A |
19: 46,751,685 (GRCm39) |
V492M |
possibly damaging |
Het |
Cntn3 |
A |
G |
6: 102,180,981 (GRCm39) |
V738A |
probably damaging |
Het |
Coq8a |
T |
C |
1: 179,997,646 (GRCm39) |
E351G |
probably damaging |
Het |
Cyp3a57 |
T |
C |
5: 145,307,538 (GRCm39) |
|
probably null |
Het |
Dbn1 |
T |
C |
13: 55,623,071 (GRCm39) |
I471V |
probably benign |
Het |
Ddx21 |
G |
T |
10: 62,429,782 (GRCm39) |
Q321K |
probably benign |
Het |
Dhx8 |
T |
C |
11: 101,630,634 (GRCm39) |
V347A |
probably damaging |
Het |
Dkc1 |
A |
G |
X: 74,144,598 (GRCm39) |
I215V |
probably benign |
Homo |
Dlg2 |
A |
G |
7: 92,077,788 (GRCm39) |
I685V |
possibly damaging |
Het |
Dusp11 |
A |
C |
6: 85,930,363 (GRCm39) |
N140K |
probably damaging |
Het |
Ece2 |
A |
G |
16: 20,459,468 (GRCm39) |
K454R |
probably damaging |
Het |
Eno4 |
T |
A |
19: 58,935,181 (GRCm39) |
V131E |
probably damaging |
Het |
Enpep |
A |
G |
3: 129,097,362 (GRCm39) |
|
probably null |
Het |
Etv1 |
T |
C |
12: 38,885,219 (GRCm39) |
Y236H |
probably damaging |
Het |
F2rl2 |
A |
G |
13: 95,837,140 (GRCm39) |
T62A |
probably benign |
Het |
Fbxl21 |
T |
C |
13: 56,684,862 (GRCm39) |
V296A |
probably damaging |
Het |
Fig4 |
T |
C |
10: 41,148,994 (GRCm39) |
I153V |
probably benign |
Het |
Fis1 |
T |
A |
5: 136,991,951 (GRCm39) |
N41K |
possibly damaging |
Het |
Fras1 |
T |
A |
5: 96,848,427 (GRCm39) |
M1814K |
probably benign |
Het |
Frem2 |
T |
A |
3: 53,451,792 (GRCm39) |
I2266F |
probably benign |
Het |
Gm10330 |
A |
T |
12: 23,829,843 (GRCm39) |
*113R |
probably null |
Het |
Gm12185 |
T |
A |
11: 48,806,367 (GRCm39) |
I275F |
probably benign |
Het |
Gsdme |
A |
T |
6: 50,206,304 (GRCm39) |
C180S |
possibly damaging |
Het |
Herc1 |
A |
G |
9: 66,323,551 (GRCm39) |
E1355G |
probably benign |
Het |
Hnrnpm |
A |
T |
17: 33,869,185 (GRCm39) |
I453N |
possibly damaging |
Het |
Hspb9 |
T |
C |
11: 100,604,896 (GRCm39) |
L74P |
probably damaging |
Het |
Ift46 |
C |
A |
9: 44,695,260 (GRCm39) |
Y85* |
probably null |
Het |
Insyn2b |
T |
G |
11: 34,353,227 (GRCm39) |
L423R |
probably damaging |
Het |
Ints3 |
T |
C |
3: 90,315,817 (GRCm39) |
T316A |
possibly damaging |
Het |
Isg20 |
C |
T |
7: 78,564,076 (GRCm39) |
|
probably benign |
Het |
Itga11 |
T |
A |
9: 62,642,639 (GRCm39) |
N187K |
probably damaging |
Het |
Klhl9 |
G |
A |
4: 88,639,161 (GRCm39) |
T360I |
probably damaging |
Het |
Krt39 |
T |
A |
11: 99,411,826 (GRCm39) |
I87F |
probably benign |
Het |
Krtap19-4 |
G |
A |
16: 88,681,734 (GRCm39) |
S74F |
unknown |
Het |
Lgi1 |
G |
A |
19: 38,289,737 (GRCm39) |
V268I |
probably damaging |
Het |
Lrrc46 |
G |
A |
11: 96,925,719 (GRCm39) |
P248S |
probably benign |
Het |
Lrrn4 |
C |
T |
2: 132,721,488 (GRCm39) |
V110I |
probably benign |
Het |
Mamstr |
C |
A |
7: 45,294,116 (GRCm39) |
|
probably benign |
Het |
Micu3 |
T |
A |
8: 40,833,718 (GRCm39) |
F451I |
probably damaging |
Het |
Mid1 |
C |
A |
X: 168,768,044 (GRCm39) |
D130E |
possibly damaging |
Het |
Mkks |
T |
C |
2: 136,722,201 (GRCm39) |
T319A |
probably benign |
Het |
Mob3c |
A |
G |
4: 115,690,968 (GRCm39) |
|
probably null |
Het |
Muc6 |
T |
C |
7: 141,230,554 (GRCm39) |
E1192G |
probably benign |
Het |
Ndc80 |
A |
G |
17: 71,827,753 (GRCm39) |
|
probably null |
Het |
Nfx1 |
A |
G |
4: 41,012,070 (GRCm39) |
K807E |
probably benign |
Het |
Nrxn1 |
A |
T |
17: 90,930,850 (GRCm39) |
L181Q |
probably damaging |
Het |
Nsun7 |
A |
G |
5: 66,418,407 (GRCm39) |
S46G |
probably benign |
Het |
Nup98 |
A |
T |
7: 101,834,038 (GRCm39) |
L308H |
probably damaging |
Het |
Or4c115 |
C |
A |
2: 88,927,860 (GRCm39) |
W137L |
probably benign |
Het |
Or52j3 |
T |
C |
7: 102,836,098 (GRCm39) |
F97L |
probably damaging |
Het |
Or6f2 |
T |
C |
7: 139,756,141 (GRCm39) |
V36A |
probably benign |
Het |
Or8k32 |
T |
C |
2: 86,369,077 (GRCm39) |
M61V |
possibly damaging |
Het |
Palb2 |
T |
C |
7: 121,726,589 (GRCm39) |
K427R |
probably damaging |
Het |
Pcdha1 |
C |
A |
18: 37,063,965 (GRCm39) |
Q210K |
probably benign |
Het |
Pcdhb2 |
T |
C |
18: 37,429,260 (GRCm39) |
L411P |
probably damaging |
Het |
Pde4dip |
C |
A |
3: 97,602,321 (GRCm39) |
D2252Y |
probably damaging |
Het |
Plekhg4 |
T |
A |
8: 106,107,003 (GRCm39) |
Y899* |
probably null |
Het |
Psmd2 |
T |
C |
16: 20,478,719 (GRCm39) |
V606A |
probably damaging |
Het |
Ptprq |
A |
T |
10: 107,521,043 (GRCm39) |
F710I |
probably benign |
Het |
Rad51ap2 |
A |
G |
12: 11,506,552 (GRCm39) |
E158G |
probably damaging |
Het |
Rasip1 |
T |
A |
7: 45,277,247 (GRCm39) |
H18Q |
possibly damaging |
Het |
Rassf8 |
A |
G |
6: 145,760,808 (GRCm39) |
K45E |
probably damaging |
Het |
Rrn3 |
T |
A |
16: 13,613,940 (GRCm39) |
M284K |
probably damaging |
Het |
Rsf1 |
GGCG |
GGCGACGGCTGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Rtn2 |
C |
A |
7: 19,027,820 (GRCm39) |
N403K |
probably damaging |
Het |
Rusc1 |
A |
G |
3: 88,997,027 (GRCm39) |
W462R |
probably damaging |
Het |
Sdc3 |
T |
A |
4: 130,545,907 (GRCm39) |
|
probably benign |
Het |
Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
Slc12a2 |
T |
A |
18: 58,039,032 (GRCm39) |
C537* |
probably null |
Het |
Slc4a2 |
G |
A |
5: 24,639,238 (GRCm39) |
|
probably null |
Het |
Spsb4 |
T |
A |
9: 96,877,744 (GRCm39) |
D193V |
probably damaging |
Het |
Strn |
A |
C |
17: 78,984,780 (GRCm39) |
F288V |
probably damaging |
Het |
Stx18 |
G |
A |
5: 38,293,712 (GRCm39) |
|
probably benign |
Het |
Tfcp2l1 |
T |
A |
1: 118,596,378 (GRCm39) |
M371K |
probably benign |
Het |
Thnsl1 |
A |
G |
2: 21,216,352 (GRCm39) |
|
probably null |
Het |
Tlr11 |
C |
T |
14: 50,598,439 (GRCm39) |
H142Y |
possibly damaging |
Het |
Tor1aip2 |
T |
A |
1: 155,940,780 (GRCm39) |
I362K |
probably damaging |
Het |
Trmt13 |
T |
C |
3: 116,383,404 (GRCm39) |
K125E |
probably damaging |
Het |
Trpm8 |
T |
C |
1: 88,264,851 (GRCm39) |
V320A |
probably benign |
Het |
Ubr3 |
A |
T |
2: 69,766,263 (GRCm39) |
H377L |
probably damaging |
Het |
Usp8 |
A |
G |
2: 126,567,349 (GRCm39) |
R123G |
probably null |
Het |
Vim |
T |
A |
2: 13,579,775 (GRCm39) |
L178Q |
probably damaging |
Het |
Vmn1r231 |
A |
C |
17: 21,110,489 (GRCm39) |
V142G |
possibly damaging |
Het |
Vmn1r83 |
A |
G |
7: 12,055,697 (GRCm39) |
M120T |
possibly damaging |
Het |
Vwce |
G |
T |
19: 10,642,012 (GRCm39) |
V913F |
possibly damaging |
Het |
Zbtb18 |
C |
A |
1: 177,275,285 (GRCm39) |
T215K |
probably benign |
Het |
Zeb2 |
A |
T |
2: 44,886,353 (GRCm39) |
D857E |
probably damaging |
Het |
Zfp106 |
G |
A |
2: 120,364,221 (GRCm39) |
H729Y |
probably damaging |
Het |
Zfp977 |
C |
A |
7: 42,229,437 (GRCm39) |
A363S |
probably benign |
Het |
|
Other mutations in Plxnb2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00546:Plxnb2
|
APN |
15 |
89,046,569 (GRCm39) |
splice site |
probably benign |
|
IGL01574:Plxnb2
|
APN |
15 |
89,046,886 (GRCm39) |
splice site |
probably null |
|
IGL01695:Plxnb2
|
APN |
15 |
89,041,417 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01763:Plxnb2
|
APN |
15 |
89,046,184 (GRCm39) |
splice site |
probably null |
|
IGL01921:Plxnb2
|
APN |
15 |
89,048,474 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02129:Plxnb2
|
APN |
15 |
89,044,613 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02153:Plxnb2
|
APN |
15 |
89,050,016 (GRCm39) |
nonsense |
probably null |
|
IGL02637:Plxnb2
|
APN |
15 |
89,048,260 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02892:Plxnb2
|
APN |
15 |
89,045,425 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03108:Plxnb2
|
APN |
15 |
89,042,234 (GRCm39) |
missense |
probably benign |
0.32 |
IGL03115:Plxnb2
|
APN |
15 |
89,046,641 (GRCm39) |
splice site |
probably benign |
|
P0040:Plxnb2
|
UTSW |
15 |
89,047,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Plxnb2
|
UTSW |
15 |
89,047,479 (GRCm39) |
critical splice donor site |
probably null |
|
R0095:Plxnb2
|
UTSW |
15 |
89,049,534 (GRCm39) |
missense |
probably benign |
|
R0103:Plxnb2
|
UTSW |
15 |
89,045,972 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0544:Plxnb2
|
UTSW |
15 |
89,042,816 (GRCm39) |
splice site |
probably benign |
|
R0671:Plxnb2
|
UTSW |
15 |
89,042,184 (GRCm39) |
missense |
probably benign |
0.14 |
R1279:Plxnb2
|
UTSW |
15 |
89,046,524 (GRCm39) |
missense |
probably benign |
0.02 |
R1530:Plxnb2
|
UTSW |
15 |
89,051,395 (GRCm39) |
missense |
probably benign |
|
R1542:Plxnb2
|
UTSW |
15 |
89,050,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R1610:Plxnb2
|
UTSW |
15 |
89,042,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R1686:Plxnb2
|
UTSW |
15 |
89,046,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R1702:Plxnb2
|
UTSW |
15 |
89,046,187 (GRCm39) |
critical splice donor site |
probably null |
|
R1996:Plxnb2
|
UTSW |
15 |
89,042,971 (GRCm39) |
missense |
probably benign |
0.13 |
R1997:Plxnb2
|
UTSW |
15 |
89,042,971 (GRCm39) |
missense |
probably benign |
0.13 |
R2031:Plxnb2
|
UTSW |
15 |
89,047,013 (GRCm39) |
nonsense |
probably null |
|
R2049:Plxnb2
|
UTSW |
15 |
89,043,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R2072:Plxnb2
|
UTSW |
15 |
89,042,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R2076:Plxnb2
|
UTSW |
15 |
89,042,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R2140:Plxnb2
|
UTSW |
15 |
89,040,765 (GRCm39) |
missense |
probably benign |
0.04 |
R2418:Plxnb2
|
UTSW |
15 |
89,045,272 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2419:Plxnb2
|
UTSW |
15 |
89,045,272 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3752:Plxnb2
|
UTSW |
15 |
89,041,458 (GRCm39) |
splice site |
probably benign |
|
R3825:Plxnb2
|
UTSW |
15 |
89,050,602 (GRCm39) |
missense |
probably benign |
0.05 |
R4154:Plxnb2
|
UTSW |
15 |
89,043,845 (GRCm39) |
missense |
probably damaging |
0.98 |
R4197:Plxnb2
|
UTSW |
15 |
89,041,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R4385:Plxnb2
|
UTSW |
15 |
89,044,826 (GRCm39) |
missense |
probably damaging |
0.96 |
R4434:Plxnb2
|
UTSW |
15 |
89,047,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R4717:Plxnb2
|
UTSW |
15 |
89,041,622 (GRCm39) |
nonsense |
probably null |
|
R4773:Plxnb2
|
UTSW |
15 |
89,051,150 (GRCm39) |
missense |
probably benign |
0.06 |
R4905:Plxnb2
|
UTSW |
15 |
89,041,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R5368:Plxnb2
|
UTSW |
15 |
89,043,796 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5418:Plxnb2
|
UTSW |
15 |
89,050,694 (GRCm39) |
missense |
probably benign |
0.00 |
R5484:Plxnb2
|
UTSW |
15 |
89,048,412 (GRCm39) |
splice site |
probably null |
|
R5520:Plxnb2
|
UTSW |
15 |
89,051,746 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5566:Plxnb2
|
UTSW |
15 |
89,048,223 (GRCm39) |
missense |
probably benign |
0.05 |
R5568:Plxnb2
|
UTSW |
15 |
89,041,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R5619:Plxnb2
|
UTSW |
15 |
89,047,012 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5685:Plxnb2
|
UTSW |
15 |
89,051,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R5688:Plxnb2
|
UTSW |
15 |
89,042,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R5809:Plxnb2
|
UTSW |
15 |
89,051,774 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5813:Plxnb2
|
UTSW |
15 |
89,044,962 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5866:Plxnb2
|
UTSW |
15 |
89,051,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R6016:Plxnb2
|
UTSW |
15 |
89,045,225 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6117:Plxnb2
|
UTSW |
15 |
89,042,203 (GRCm39) |
missense |
probably benign |
0.04 |
R6187:Plxnb2
|
UTSW |
15 |
89,051,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Plxnb2
|
UTSW |
15 |
89,049,494 (GRCm39) |
missense |
probably benign |
0.22 |
R6263:Plxnb2
|
UTSW |
15 |
89,046,189 (GRCm39) |
missense |
probably damaging |
0.99 |
R6269:Plxnb2
|
UTSW |
15 |
89,044,916 (GRCm39) |
missense |
probably benign |
0.18 |
R6351:Plxnb2
|
UTSW |
15 |
89,041,973 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6522:Plxnb2
|
UTSW |
15 |
89,048,629 (GRCm39) |
missense |
probably benign |
0.18 |
R6856:Plxnb2
|
UTSW |
15 |
89,048,523 (GRCm39) |
missense |
probably benign |
0.27 |
R6930:Plxnb2
|
UTSW |
15 |
89,044,592 (GRCm39) |
missense |
probably benign |
|
R7354:Plxnb2
|
UTSW |
15 |
89,049,928 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7513:Plxnb2
|
UTSW |
15 |
89,042,525 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7522:Plxnb2
|
UTSW |
15 |
89,045,977 (GRCm39) |
missense |
probably benign |
0.20 |
R7730:Plxnb2
|
UTSW |
15 |
89,046,533 (GRCm39) |
missense |
probably benign |
|
R7766:Plxnb2
|
UTSW |
15 |
89,045,474 (GRCm39) |
missense |
probably benign |
0.01 |
R7781:Plxnb2
|
UTSW |
15 |
89,041,225 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8126:Plxnb2
|
UTSW |
15 |
89,047,506 (GRCm39) |
missense |
probably benign |
|
R8131:Plxnb2
|
UTSW |
15 |
89,042,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R8372:Plxnb2
|
UTSW |
15 |
89,042,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R8736:Plxnb2
|
UTSW |
15 |
89,046,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R8772:Plxnb2
|
UTSW |
15 |
89,046,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R9022:Plxnb2
|
UTSW |
15 |
89,048,471 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9044:Plxnb2
|
UTSW |
15 |
89,044,566 (GRCm39) |
splice site |
probably benign |
|
R9253:Plxnb2
|
UTSW |
15 |
89,052,015 (GRCm39) |
missense |
probably benign |
|
R9398:Plxnb2
|
UTSW |
15 |
89,045,122 (GRCm39) |
missense |
probably benign |
0.02 |
R9562:Plxnb2
|
UTSW |
15 |
89,050,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R9568:Plxnb2
|
UTSW |
15 |
89,045,160 (GRCm39) |
nonsense |
probably null |
|
R9613:Plxnb2
|
UTSW |
15 |
89,048,496 (GRCm39) |
missense |
probably benign |
0.01 |
X0027:Plxnb2
|
UTSW |
15 |
89,044,916 (GRCm39) |
missense |
probably benign |
0.18 |
Z1177:Plxnb2
|
UTSW |
15 |
89,043,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|