Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
G |
A |
3: 137,774,156 (GRCm39) |
S1115N |
probably damaging |
Het |
Abca1 |
A |
G |
4: 53,059,303 (GRCm39) |
V1551A |
probably benign |
Het |
Adam30 |
T |
C |
3: 98,070,291 (GRCm39) |
I708T |
probably benign |
Het |
Aknad1 |
T |
A |
3: 108,659,328 (GRCm39) |
L114H |
possibly damaging |
Het |
Akr1c18 |
G |
A |
13: 4,185,262 (GRCm39) |
S290L |
probably benign |
Het |
Aldh18a1 |
G |
T |
19: 40,545,881 (GRCm39) |
D635E |
probably benign |
Het |
Bax |
G |
T |
7: 45,115,698 (GRCm39) |
P23Q |
probably null |
Het |
Bhlha15 |
A |
T |
5: 144,128,244 (GRCm39) |
N119Y |
probably damaging |
Het |
Boll |
T |
A |
1: 55,402,478 (GRCm39) |
M1L |
probably benign |
Het |
C2cd2 |
A |
T |
16: 97,693,502 (GRCm39) |
I123N |
probably benign |
Het |
Cacnb4 |
A |
C |
2: 52,364,997 (GRCm39) |
S89A |
probably benign |
Het |
Calca |
A |
G |
7: 114,234,387 (GRCm39) |
C21R |
probably benign |
Het |
Calcr |
T |
C |
6: 3,693,899 (GRCm39) |
I325M |
probably benign |
Het |
Card14 |
T |
A |
11: 119,212,718 (GRCm39) |
F94Y |
probably damaging |
Het |
Chil3 |
A |
C |
3: 106,057,203 (GRCm39) |
I247S |
probably damaging |
Het |
Clca3b |
T |
C |
3: 144,544,898 (GRCm39) |
N363S |
probably benign |
Het |
Cnksr3 |
A |
G |
10: 7,070,475 (GRCm39) |
V494A |
possibly damaging |
Het |
Cog4 |
A |
G |
8: 111,578,717 (GRCm39) |
|
probably null |
Het |
Crybg1 |
T |
A |
10: 43,862,322 (GRCm39) |
Y1484F |
probably damaging |
Het |
Dglucy |
A |
G |
12: 100,816,370 (GRCm39) |
|
probably null |
Het |
Dmp1 |
T |
A |
5: 104,359,380 (GRCm39) |
|
probably null |
Het |
Dscaml1 |
T |
A |
9: 45,658,140 (GRCm39) |
I1637N |
possibly damaging |
Het |
Ercc6 |
T |
A |
14: 32,279,905 (GRCm39) |
I640N |
probably damaging |
Het |
Esp16 |
G |
T |
17: 39,850,707 (GRCm39) |
E29* |
probably null |
Het |
Fam149a |
T |
C |
8: 45,834,755 (GRCm39) |
I15V |
possibly damaging |
Het |
Flt4 |
T |
A |
11: 49,525,723 (GRCm39) |
I724N |
probably damaging |
Het |
Glb1 |
C |
T |
9: 114,259,429 (GRCm39) |
R202C |
probably damaging |
Het |
Gmpr2 |
C |
A |
14: 55,910,441 (GRCm39) |
S41* |
probably null |
Het |
Golgb1 |
T |
A |
16: 36,737,192 (GRCm39) |
D2187E |
probably damaging |
Het |
Gpsm2 |
A |
G |
3: 108,597,080 (GRCm39) |
|
probably null |
Het |
Helz |
A |
G |
11: 107,563,399 (GRCm39) |
D1613G |
unknown |
Het |
Hemgn |
A |
C |
4: 46,396,504 (GRCm39) |
M244R |
possibly damaging |
Het |
Hsd3b1 |
A |
T |
3: 98,763,453 (GRCm39) |
V56E |
probably damaging |
Het |
Jup |
A |
T |
11: 100,267,751 (GRCm39) |
I524N |
probably damaging |
Het |
Kdm1b |
G |
T |
13: 47,205,377 (GRCm39) |
|
probably null |
Het |
Kif11 |
A |
T |
19: 37,379,095 (GRCm39) |
|
probably null |
Het |
Lars1 |
A |
T |
18: 42,361,835 (GRCm39) |
W591R |
probably damaging |
Het |
Med12l |
A |
C |
3: 59,169,389 (GRCm39) |
D1593A |
probably damaging |
Het |
Med17 |
A |
T |
9: 15,188,928 (GRCm39) |
D112E |
possibly damaging |
Het |
Mettl2 |
T |
A |
11: 105,019,866 (GRCm39) |
F168I |
probably benign |
Het |
Mmp9 |
A |
T |
2: 164,792,365 (GRCm39) |
D323V |
probably damaging |
Het |
Mpzl2 |
C |
T |
9: 44,961,006 (GRCm39) |
T214I |
probably benign |
Het |
Ms4a15 |
T |
C |
19: 10,958,670 (GRCm39) |
H134R |
probably benign |
Het |
Ms4a6d |
T |
A |
19: 11,580,653 (GRCm39) |
I2F |
probably damaging |
Het |
Muc3a |
G |
A |
5: 137,244,535 (GRCm39) |
P206S |
unknown |
Het |
Nectin2 |
C |
A |
7: 19,458,733 (GRCm39) |
L359F |
probably damaging |
Het |
Or2y6 |
C |
A |
11: 52,104,096 (GRCm39) |
C240F |
probably damaging |
Het |
Or4f53 |
T |
A |
2: 111,087,918 (GRCm39) |
F153I |
probably benign |
Het |
Pgm2 |
G |
T |
5: 64,269,467 (GRCm39) |
C518F |
possibly damaging |
Het |
Plppr4 |
A |
G |
3: 117,116,114 (GRCm39) |
V581A |
probably damaging |
Het |
Prkra |
G |
C |
2: 76,469,634 (GRCm39) |
L142V |
probably damaging |
Het |
Prpf38a |
G |
A |
4: 108,434,195 (GRCm39) |
T74I |
probably benign |
Het |
Ptprs |
T |
A |
17: 56,736,064 (GRCm39) |
N635I |
probably damaging |
Het |
Rxfp2 |
A |
G |
5: 149,987,201 (GRCm39) |
N361D |
probably benign |
Het |
Ryr3 |
T |
G |
2: 112,608,588 (GRCm39) |
I2351L |
probably damaging |
Het |
Sfmbt2 |
A |
T |
2: 10,580,190 (GRCm39) |
T618S |
probably benign |
Het |
Six6 |
A |
G |
12: 72,986,906 (GRCm39) |
D26G |
probably damaging |
Het |
Slc20a1 |
T |
C |
2: 129,051,047 (GRCm39) |
L568P |
probably damaging |
Het |
Slx4ip |
T |
A |
2: 136,842,104 (GRCm39) |
C10S |
probably damaging |
Het |
Sox13 |
G |
T |
1: 133,311,498 (GRCm39) |
T578K |
probably benign |
Het |
Spire2 |
A |
T |
8: 124,088,042 (GRCm39) |
S509C |
probably damaging |
Het |
Sptbn4 |
T |
C |
7: 27,074,808 (GRCm39) |
D1521G |
possibly damaging |
Het |
Sult2a7 |
T |
C |
7: 14,204,098 (GRCm39) |
T207A |
probably benign |
Het |
Sun2 |
A |
G |
15: 79,609,721 (GRCm39) |
I708T |
probably damaging |
Het |
Supt5 |
T |
C |
7: 28,030,899 (GRCm39) |
E44G |
unknown |
Het |
Thsd1 |
A |
G |
8: 22,733,022 (GRCm39) |
E23G |
probably damaging |
Het |
Ticrr |
T |
C |
7: 79,310,728 (GRCm39) |
V214A |
possibly damaging |
Het |
Vmn2r74 |
A |
T |
7: 85,605,324 (GRCm39) |
F441L |
probably damaging |
Het |
Zfp30 |
A |
G |
7: 29,493,080 (GRCm39) |
T526A |
probably benign |
Het |
Zfp518a |
G |
T |
19: 40,902,415 (GRCm39) |
Q781H |
probably damaging |
Het |
Zmynd11 |
A |
G |
13: 9,739,687 (GRCm39) |
V434A |
probably benign |
Het |
Zranb1 |
A |
G |
7: 132,585,508 (GRCm39) |
D652G |
probably damaging |
Het |
|
Other mutations in Lrtm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02191:Lrtm1
|
APN |
14 |
28,743,906 (GRCm39) |
missense |
probably benign |
0.00 |
R0102:Lrtm1
|
UTSW |
14 |
28,744,184 (GRCm39) |
splice site |
probably benign |
|
R0102:Lrtm1
|
UTSW |
14 |
28,744,184 (GRCm39) |
splice site |
probably benign |
|
R0602:Lrtm1
|
UTSW |
14 |
28,744,179 (GRCm39) |
splice site |
probably benign |
|
R5214:Lrtm1
|
UTSW |
14 |
28,743,651 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5253:Lrtm1
|
UTSW |
14 |
28,743,801 (GRCm39) |
missense |
probably benign |
0.13 |
R5787:Lrtm1
|
UTSW |
14 |
28,743,947 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5937:Lrtm1
|
UTSW |
14 |
28,743,787 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6238:Lrtm1
|
UTSW |
14 |
28,749,628 (GRCm39) |
missense |
probably benign |
0.02 |
R6850:Lrtm1
|
UTSW |
14 |
28,749,407 (GRCm39) |
missense |
probably benign |
0.00 |
R7304:Lrtm1
|
UTSW |
14 |
28,744,075 (GRCm39) |
missense |
probably damaging |
0.97 |
R7363:Lrtm1
|
UTSW |
14 |
28,743,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R7385:Lrtm1
|
UTSW |
14 |
28,749,673 (GRCm39) |
missense |
probably benign |
0.00 |
R9299:Lrtm1
|
UTSW |
14 |
28,743,714 (GRCm39) |
missense |
probably damaging |
1.00 |
RF036:Lrtm1
|
UTSW |
14 |
28,743,400 (GRCm39) |
frame shift |
probably null |
|
RF063:Lrtm1
|
UTSW |
14 |
28,743,400 (GRCm39) |
frame shift |
probably null |
|
|