Other mutations in this stock |
Total: 119 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss2 |
T |
C |
2: 155,360,186 (GRCm39) |
S54P |
probably damaging |
Het |
Ahnak2 |
T |
C |
12: 112,746,605 (GRCm39) |
K1242E |
|
Het |
Alpi |
T |
A |
1: 87,029,257 (GRCm39) |
M1L |
possibly damaging |
Het |
Atp2c1 |
C |
T |
9: 105,329,982 (GRCm39) |
A283T |
probably damaging |
Het |
Atp8b5 |
T |
G |
4: 43,366,021 (GRCm39) |
M764R |
probably benign |
Het |
B4galnt2 |
T |
A |
11: 95,760,193 (GRCm39) |
H278L |
probably damaging |
Het |
Bcl9l |
G |
T |
9: 44,420,634 (GRCm39) |
A1347S |
probably benign |
Het |
Bicd2 |
A |
G |
13: 49,533,427 (GRCm39) |
E671G |
probably damaging |
Het |
Bmp3 |
A |
T |
5: 99,020,077 (GRCm39) |
I167F |
probably damaging |
Het |
Bpifb5 |
T |
A |
2: 154,072,105 (GRCm39) |
C271S |
possibly damaging |
Het |
Camsap2 |
T |
A |
1: 136,198,644 (GRCm39) |
H793L |
|
Het |
Casp8ap2 |
T |
A |
4: 32,643,974 (GRCm39) |
S1016T |
possibly damaging |
Het |
Castor1 |
A |
G |
11: 4,171,897 (GRCm39) |
S325G |
not run |
Het |
Ccdc134 |
T |
A |
15: 82,025,149 (GRCm39) |
I216N |
possibly damaging |
Het |
Ccdc63 |
G |
T |
5: 122,246,245 (GRCm39) |
R559S |
probably benign |
Het |
Cd276 |
T |
C |
9: 58,442,895 (GRCm39) |
T187A |
probably benign |
Het |
Ciao1 |
C |
T |
2: 127,087,678 (GRCm39) |
R219H |
probably damaging |
Het |
Clmn |
T |
C |
12: 104,751,687 (GRCm39) |
D256G |
possibly damaging |
Het |
Cobl |
A |
C |
11: 12,206,225 (GRCm39) |
M550R |
possibly damaging |
Het |
Cracr2b |
A |
T |
7: 141,044,118 (GRCm39) |
T117S |
probably benign |
Het |
Cx3cr1 |
G |
A |
9: 119,881,282 (GRCm39) |
A40V |
probably benign |
Het |
Cxcl14 |
A |
G |
13: 56,440,344 (GRCm39) |
C72R |
probably damaging |
Het |
Dab2 |
T |
A |
15: 6,451,747 (GRCm39) |
I121N |
probably damaging |
Het |
Dapk1 |
A |
G |
13: 60,898,990 (GRCm39) |
Y820C |
probably damaging |
Het |
Dele1 |
A |
G |
18: 38,390,319 (GRCm39) |
N256D |
probably damaging |
Het |
Ech1 |
T |
A |
7: 28,525,623 (GRCm39) |
C91S |
probably damaging |
Het |
Exosc5 |
T |
G |
7: 25,358,734 (GRCm39) |
V25G |
probably benign |
Het |
Fbp1 |
A |
C |
13: 63,020,564 (GRCm39) |
D122E |
possibly damaging |
Het |
Fbxw13 |
A |
G |
9: 109,014,471 (GRCm39) |
Y101H |
unknown |
Het |
Fcsk |
C |
T |
8: 111,616,963 (GRCm39) |
G396S |
possibly damaging |
Het |
Fhip1a |
G |
A |
3: 85,579,871 (GRCm39) |
S778L |
probably benign |
Het |
Fmnl1 |
T |
A |
11: 103,077,453 (GRCm39) |
V271E |
probably damaging |
Het |
Galnt1 |
T |
A |
18: 24,417,866 (GRCm39) |
S545T |
probably benign |
Het |
Galnt13 |
G |
A |
2: 54,406,576 (GRCm39) |
V9M |
possibly damaging |
Het |
Gm7995 |
A |
T |
14: 42,132,302 (GRCm39) |
I45F |
|
Het |
Gpr137 |
C |
T |
19: 6,917,726 (GRCm39) |
R134Q |
possibly damaging |
Het |
Gpr22 |
T |
G |
12: 31,759,514 (GRCm39) |
I203L |
probably benign |
Het |
H2-Q10 |
T |
C |
17: 35,784,457 (GRCm39) |
Y324H |
not run |
Het |
Hcn4 |
G |
A |
9: 58,751,582 (GRCm39) |
E403K |
unknown |
Het |
Hddc2 |
T |
A |
10: 31,189,412 (GRCm39) |
M1K |
probably null |
Het |
Hps3 |
A |
G |
3: 20,089,329 (GRCm39) |
F34S |
probably damaging |
Het |
Ift56 |
T |
A |
6: 38,381,422 (GRCm39) |
Y319* |
probably null |
Het |
Igdcc4 |
G |
T |
9: 65,031,276 (GRCm39) |
V405L |
possibly damaging |
Het |
Itpr2 |
C |
A |
6: 146,231,006 (GRCm39) |
V1215L |
probably damaging |
Het |
Kif26b |
T |
C |
1: 178,742,339 (GRCm39) |
S812P |
probably damaging |
Het |
Lgi1 |
T |
A |
19: 38,289,713 (GRCm39) |
C260S |
probably damaging |
Het |
Lhfpl6 |
A |
G |
3: 53,168,020 (GRCm39) |
Y198C |
probably damaging |
Het |
Lrp5 |
T |
C |
19: 3,699,439 (GRCm39) |
D282G |
probably benign |
Het |
Lrpprc |
T |
C |
17: 85,079,567 (GRCm39) |
T230A |
probably damaging |
Het |
Maco1 |
A |
T |
4: 134,555,590 (GRCm39) |
N294K |
possibly damaging |
Het |
Magi2 |
G |
A |
5: 20,563,954 (GRCm39) |
G199D |
probably damaging |
Het |
Map1b |
C |
T |
13: 99,644,648 (GRCm39) |
R85Q |
probably damaging |
Het |
Marchf7 |
T |
A |
2: 60,077,858 (GRCm39) |
|
probably null |
Het |
Morc1 |
A |
G |
16: 48,251,708 (GRCm39) |
D2G |
probably damaging |
Het |
Mpp7 |
A |
T |
18: 7,351,079 (GRCm39) |
F539L |
probably damaging |
Het |
Muc13 |
A |
T |
16: 33,634,951 (GRCm39) |
I502F |
probably damaging |
Het |
Myh13 |
A |
G |
11: 67,255,286 (GRCm39) |
|
probably null |
Het |
Nat10 |
C |
G |
2: 103,578,390 (GRCm39) |
L238F |
probably damaging |
Het |
Nckap1 |
G |
A |
2: 80,354,885 (GRCm39) |
T679I |
probably damaging |
Het |
Npy6r |
T |
A |
18: 44,409,260 (GRCm39) |
I227N |
probably damaging |
Het |
Nudt18 |
A |
T |
14: 70,815,389 (GRCm39) |
M1L |
unknown |
Het |
Or13d1 |
T |
A |
4: 52,971,207 (GRCm39) |
N195K |
probably damaging |
Het |
Or14a257 |
G |
A |
7: 86,138,417 (GRCm39) |
T114I |
probably damaging |
Het |
Or4f14 |
T |
A |
2: 111,742,637 (GRCm39) |
I213L |
probably benign |
Het |
Or8d1 |
C |
A |
9: 38,766,412 (GRCm39) |
T18K |
probably damaging |
Het |
Or8u8 |
T |
C |
2: 86,011,678 (GRCm39) |
Y259C |
probably damaging |
Het |
Pcdha3 |
T |
A |
18: 37,079,266 (GRCm39) |
F3I |
probably benign |
Het |
Pcdhga3 |
T |
A |
18: 37,808,917 (GRCm39) |
Y457N |
possibly damaging |
Het |
Pclo |
A |
T |
5: 14,719,631 (GRCm39) |
Q1256L |
unknown |
Het |
Piezo2 |
C |
T |
18: 63,157,543 (GRCm39) |
R2389H |
probably damaging |
Het |
Pml |
G |
T |
9: 58,154,496 (GRCm39) |
Q126K |
probably benign |
Het |
Ppef2 |
A |
G |
5: 92,376,563 (GRCm39) |
Y655H |
probably damaging |
Het |
Ppp4r1 |
T |
C |
17: 66,147,936 (GRCm39) |
V926A |
probably damaging |
Het |
Psg29 |
A |
G |
7: 16,945,648 (GRCm39) |
D406G |
possibly damaging |
Het |
Ptprf |
T |
C |
4: 118,092,864 (GRCm39) |
D517G |
probably benign |
Het |
Ptprg |
G |
A |
14: 12,142,461 (GRCm38) |
E371K |
probably benign |
Het |
Pttg1ip2 |
T |
C |
5: 5,505,952 (GRCm39) |
I110V |
probably benign |
Het |
Rasgrp1 |
T |
C |
2: 117,118,424 (GRCm39) |
I522V |
probably damaging |
Het |
Rasgrp1 |
T |
A |
2: 117,122,178 (GRCm39) |
D404V |
possibly damaging |
Het |
Rb1cc1 |
T |
A |
1: 6,315,727 (GRCm39) |
F541I |
probably damaging |
Het |
Rgsl1 |
C |
A |
1: 153,719,847 (GRCm39) |
|
probably null |
Het |
Rhobtb2 |
C |
T |
14: 70,033,397 (GRCm39) |
W524* |
probably null |
Het |
Rhox4d |
G |
A |
X: 36,700,645 (GRCm39) |
G191E |
unknown |
Het |
Rims1 |
A |
G |
1: 22,474,699 (GRCm39) |
S211P |
|
Het |
Ripor2 |
A |
T |
13: 24,854,054 (GRCm39) |
Q54L |
possibly damaging |
Het |
Rnf213 |
A |
G |
11: 119,372,117 (GRCm39) |
I4903V |
|
Het |
Robo3 |
T |
A |
9: 37,336,111 (GRCm39) |
I452F |
possibly damaging |
Het |
Rpl27rt |
A |
G |
18: 34,870,580 (GRCm39) |
K38R |
probably damaging |
Het |
Seh1l |
C |
T |
18: 67,916,988 (GRCm39) |
H56Y |
probably damaging |
Het |
Sema3b |
T |
A |
9: 107,480,162 (GRCm39) |
D192V |
probably damaging |
Het |
Sidt1 |
A |
T |
16: 44,106,763 (GRCm39) |
C222* |
probably null |
Het |
Skor1 |
A |
G |
9: 63,053,385 (GRCm39) |
F195L |
probably damaging |
Het |
Slc44a2 |
A |
C |
9: 21,259,642 (GRCm39) |
K596N |
possibly damaging |
Het |
Smgc |
A |
G |
15: 91,729,696 (GRCm39) |
K217E |
probably benign |
Het |
Socs7 |
C |
A |
11: 97,267,917 (GRCm39) |
H349Q |
possibly damaging |
Het |
Speer4f2 |
A |
G |
5: 17,581,540 (GRCm39) |
T161A |
|
Het |
Spg11 |
T |
C |
2: 121,924,026 (GRCm39) |
|
probably null |
Het |
Ssb |
A |
G |
2: 69,693,624 (GRCm39) |
T11A |
probably benign |
Het |
Sun1 |
A |
G |
5: 139,232,589 (GRCm39) |
S837G |
probably damaging |
Het |
Szt2 |
A |
C |
4: 118,220,668 (GRCm39) |
S3385A |
unknown |
Het |
Tapbp |
T |
C |
17: 34,139,391 (GRCm39) |
V129A |
possibly damaging |
Het |
Thsd1 |
T |
C |
8: 22,733,349 (GRCm39) |
I132T |
possibly damaging |
Het |
Tm6sf2 |
T |
A |
8: 70,530,589 (GRCm39) |
V223E |
possibly damaging |
Het |
Tm9sf4 |
T |
A |
2: 153,036,267 (GRCm39) |
M343K |
probably benign |
Het |
Trank1 |
C |
A |
9: 111,195,417 (GRCm39) |
P1147Q |
probably benign |
Het |
Trip4 |
G |
A |
9: 65,773,757 (GRCm39) |
T275M |
probably damaging |
Het |
Tsen34 |
T |
C |
7: 3,698,834 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,680,422 (GRCm39) |
E1086G |
unknown |
Het |
Ubr4 |
A |
T |
4: 139,189,778 (GRCm39) |
M853L |
unknown |
Het |
Ubxn11 |
A |
T |
4: 133,852,466 (GRCm39) |
R352W |
probably damaging |
Het |
Vmn1r35 |
G |
A |
6: 66,656,219 (GRCm39) |
|
probably benign |
Het |
Vmn2r107 |
C |
T |
17: 20,595,994 (GRCm39) |
T849I |
probably benign |
Het |
Vmn2r93 |
C |
A |
17: 18,546,248 (GRCm39) |
L707I |
probably benign |
Het |
Wwc1 |
G |
A |
11: 35,766,533 (GRCm39) |
T574I |
probably benign |
Het |
Zfp143 |
A |
G |
7: 109,669,705 (GRCm39) |
M45V |
probably benign |
Het |
Zfp518a |
T |
A |
19: 40,902,601 (GRCm39) |
N843K |
possibly damaging |
Het |
Zfp87 |
A |
T |
13: 67,665,163 (GRCm39) |
M433K |
probably benign |
Het |
Zfp873 |
C |
A |
10: 81,896,461 (GRCm39) |
H397Q |
probably damaging |
Het |
Zscan21 |
A |
T |
5: 138,116,110 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Lrtm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01089:Lrtm2
|
APN |
6 |
119,297,753 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02619:Lrtm2
|
APN |
6 |
119,294,199 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02694:Lrtm2
|
APN |
6 |
119,297,846 (GRCm39) |
missense |
possibly damaging |
0.80 |
1mM(1):Lrtm2
|
UTSW |
6 |
119,294,252 (GRCm39) |
missense |
probably damaging |
0.99 |
R0458:Lrtm2
|
UTSW |
6 |
119,294,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R1183:Lrtm2
|
UTSW |
6 |
119,297,846 (GRCm39) |
missense |
probably benign |
0.02 |
R1502:Lrtm2
|
UTSW |
6 |
119,294,235 (GRCm39) |
missense |
probably benign |
0.02 |
R3801:Lrtm2
|
UTSW |
6 |
119,294,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R4373:Lrtm2
|
UTSW |
6 |
119,297,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5126:Lrtm2
|
UTSW |
6 |
119,294,400 (GRCm39) |
missense |
probably benign |
0.04 |
R6366:Lrtm2
|
UTSW |
6 |
119,294,238 (GRCm39) |
missense |
probably damaging |
0.99 |
R7177:Lrtm2
|
UTSW |
6 |
119,294,113 (GRCm39) |
missense |
probably damaging |
0.99 |
R7442:Lrtm2
|
UTSW |
6 |
119,294,392 (GRCm39) |
missense |
probably damaging |
0.99 |
R7921:Lrtm2
|
UTSW |
6 |
119,294,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7936:Lrtm2
|
UTSW |
6 |
119,297,394 (GRCm39) |
missense |
probably benign |
0.01 |
R8204:Lrtm2
|
UTSW |
6 |
119,294,369 (GRCm39) |
missense |
probably benign |
0.03 |
R8239:Lrtm2
|
UTSW |
6 |
119,297,778 (GRCm39) |
missense |
probably damaging |
0.99 |
R8364:Lrtm2
|
UTSW |
6 |
119,294,259 (GRCm39) |
missense |
probably benign |
0.14 |
R8415:Lrtm2
|
UTSW |
6 |
119,294,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R8823:Lrtm2
|
UTSW |
6 |
119,294,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R9014:Lrtm2
|
UTSW |
6 |
119,294,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R9183:Lrtm2
|
UTSW |
6 |
119,294,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R9290:Lrtm2
|
UTSW |
6 |
119,297,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R9329:Lrtm2
|
UTSW |
6 |
119,297,412 (GRCm39) |
nonsense |
probably null |
|
R9342:Lrtm2
|
UTSW |
6 |
119,297,934 (GRCm39) |
missense |
probably benign |
|
R9390:Lrtm2
|
UTSW |
6 |
119,297,948 (GRCm39) |
missense |
probably benign |
|
|