Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
T |
C |
11: 109,932,992 (GRCm39) |
I1211V |
probably benign |
Het |
Adgre4 |
A |
G |
17: 56,124,090 (GRCm39) |
S497G |
probably damaging |
Het |
Ankrd55 |
T |
C |
13: 112,459,601 (GRCm39) |
M65T |
possibly damaging |
Het |
Entrep3 |
A |
G |
3: 89,092,888 (GRCm39) |
T257A |
probably damaging |
Het |
Ermard |
A |
G |
17: 15,271,855 (GRCm39) |
D338G |
possibly damaging |
Het |
Espl1 |
T |
C |
15: 102,221,660 (GRCm39) |
L983P |
probably damaging |
Het |
Ext2 |
A |
C |
2: 93,642,294 (GRCm39) |
L192V |
probably damaging |
Het |
Fam83b |
T |
A |
9: 76,409,403 (GRCm39) |
Y241F |
probably benign |
Het |
Fbxl12 |
G |
A |
9: 20,550,215 (GRCm39) |
P170S |
possibly damaging |
Het |
Fsip2 |
C |
A |
2: 82,807,622 (GRCm39) |
P1314T |
possibly damaging |
Het |
Greb1l |
A |
G |
18: 10,522,144 (GRCm39) |
R747G |
probably benign |
Het |
Hspa1a |
G |
T |
17: 35,189,500 (GRCm39) |
P468T |
probably damaging |
Het |
Lcn8 |
C |
T |
2: 25,544,198 (GRCm39) |
A40V |
possibly damaging |
Het |
Lmbrd2 |
A |
G |
15: 9,165,906 (GRCm39) |
Y260C |
possibly damaging |
Het |
Mex3d |
G |
T |
10: 80,217,869 (GRCm39) |
N449K |
possibly damaging |
Het |
Mgat4f |
A |
G |
1: 134,317,696 (GRCm39) |
N156S |
probably damaging |
Het |
Ncam2 |
A |
G |
16: 81,309,823 (GRCm39) |
K438E |
possibly damaging |
Het |
Nudt7 |
A |
G |
8: 114,874,625 (GRCm39) |
|
probably benign |
Het |
Nup214 |
C |
A |
2: 31,941,084 (GRCm39) |
S39* |
probably null |
Het |
Opn5 |
A |
G |
17: 42,918,089 (GRCm39) |
S58P |
probably damaging |
Het |
Or6c74 |
T |
C |
10: 129,870,052 (GRCm39) |
S186P |
probably damaging |
Het |
Or7e173 |
T |
C |
9: 19,938,704 (GRCm39) |
I177V |
possibly damaging |
Het |
Pcsk1 |
T |
A |
13: 75,280,426 (GRCm39) |
N750K |
probably benign |
Het |
Pdzrn3 |
T |
C |
6: 101,127,502 (GRCm39) |
N1055D |
probably damaging |
Het |
Phf2 |
T |
A |
13: 48,959,355 (GRCm39) |
K884* |
probably null |
Het |
Prkdc |
A |
G |
16: 15,470,166 (GRCm39) |
N191S |
probably benign |
Het |
Prpf8 |
A |
T |
11: 75,386,472 (GRCm39) |
Q987L |
probably damaging |
Het |
Prrc2c |
G |
A |
1: 162,538,355 (GRCm39) |
P425L |
probably damaging |
Het |
Rab36 |
T |
C |
10: 74,886,520 (GRCm39) |
I166T |
possibly damaging |
Het |
Rab3gap1 |
G |
T |
1: 127,855,745 (GRCm39) |
L461F |
possibly damaging |
Het |
Rnls |
A |
T |
19: 33,368,499 (GRCm39) |
Y27N |
possibly damaging |
Het |
Sncaip |
A |
T |
18: 53,002,006 (GRCm39) |
I176F |
possibly damaging |
Het |
Tagap |
G |
A |
17: 8,151,780 (GRCm39) |
G322S |
probably benign |
Het |
Tas2r130 |
C |
T |
6: 131,607,046 (GRCm39) |
A250T |
probably benign |
Het |
Tgs1 |
A |
G |
4: 3,593,632 (GRCm39) |
S507G |
probably null |
Het |
Ttn |
T |
C |
2: 76,706,056 (GRCm39) |
|
probably benign |
Het |
Zp2 |
T |
C |
7: 119,737,548 (GRCm39) |
K246E |
possibly damaging |
Het |
|
Other mutations in Lamb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00932:Lamb1
|
APN |
12 |
31,348,825 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL00939:Lamb1
|
APN |
12 |
31,352,926 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01017:Lamb1
|
APN |
12 |
31,351,063 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01384:Lamb1
|
APN |
12 |
31,370,930 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01470:Lamb1
|
APN |
12 |
31,350,261 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02207:Lamb1
|
APN |
12 |
31,379,434 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02271:Lamb1
|
APN |
12 |
31,350,250 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02272:Lamb1
|
APN |
12 |
31,355,768 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02365:Lamb1
|
APN |
12 |
31,368,344 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02471:Lamb1
|
APN |
12 |
31,370,907 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02704:Lamb1
|
APN |
12 |
31,368,466 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03132:Lamb1
|
APN |
12 |
31,350,333 (GRCm39) |
splice site |
probably null |
|
IGL03161:Lamb1
|
APN |
12 |
31,376,255 (GRCm39) |
missense |
probably benign |
0.41 |
IGL03169:Lamb1
|
APN |
12 |
31,373,645 (GRCm39) |
missense |
probably damaging |
1.00 |
Crush
|
UTSW |
12 |
31,337,423 (GRCm39) |
missense |
probably damaging |
1.00 |
Deflationary
|
UTSW |
12 |
31,371,074 (GRCm39) |
missense |
probably null |
0.63 |
E0374:Lamb1
|
UTSW |
12 |
31,337,929 (GRCm39) |
missense |
probably damaging |
1.00 |
P0043:Lamb1
|
UTSW |
12 |
31,328,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R0031:Lamb1
|
UTSW |
12 |
31,351,155 (GRCm39) |
missense |
probably benign |
0.04 |
R0047:Lamb1
|
UTSW |
12 |
31,328,600 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0047:Lamb1
|
UTSW |
12 |
31,328,600 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0285:Lamb1
|
UTSW |
12 |
31,376,644 (GRCm39) |
nonsense |
probably null |
|
R0456:Lamb1
|
UTSW |
12 |
31,354,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R0477:Lamb1
|
UTSW |
12 |
31,376,268 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0480:Lamb1
|
UTSW |
12 |
31,332,720 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0544:Lamb1
|
UTSW |
12 |
31,332,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R0565:Lamb1
|
UTSW |
12 |
31,348,914 (GRCm39) |
missense |
probably benign |
0.02 |
R1500:Lamb1
|
UTSW |
12 |
31,348,948 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1624:Lamb1
|
UTSW |
12 |
31,328,651 (GRCm39) |
critical splice donor site |
probably null |
|
R1772:Lamb1
|
UTSW |
12 |
31,328,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Lamb1
|
UTSW |
12 |
31,351,093 (GRCm39) |
missense |
probably benign |
0.00 |
R1853:Lamb1
|
UTSW |
12 |
31,368,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R1854:Lamb1
|
UTSW |
12 |
31,368,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Lamb1
|
UTSW |
12 |
31,379,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R2091:Lamb1
|
UTSW |
12 |
31,337,428 (GRCm39) |
missense |
probably damaging |
0.98 |
R2186:Lamb1
|
UTSW |
12 |
31,368,466 (GRCm39) |
nonsense |
probably null |
|
R2268:Lamb1
|
UTSW |
12 |
31,377,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Lamb1
|
UTSW |
12 |
31,319,054 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2698:Lamb1
|
UTSW |
12 |
31,348,882 (GRCm39) |
missense |
probably benign |
0.10 |
R3121:Lamb1
|
UTSW |
12 |
31,337,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R3405:Lamb1
|
UTSW |
12 |
31,337,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R3406:Lamb1
|
UTSW |
12 |
31,337,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R3608:Lamb1
|
UTSW |
12 |
31,337,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R3725:Lamb1
|
UTSW |
12 |
31,371,074 (GRCm39) |
missense |
probably null |
0.63 |
R3726:Lamb1
|
UTSW |
12 |
31,371,074 (GRCm39) |
missense |
probably null |
0.63 |
R3949:Lamb1
|
UTSW |
12 |
31,332,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R4308:Lamb1
|
UTSW |
12 |
31,379,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Lamb1
|
UTSW |
12 |
31,373,528 (GRCm39) |
missense |
probably benign |
0.00 |
R4604:Lamb1
|
UTSW |
12 |
31,328,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Lamb1
|
UTSW |
12 |
31,316,847 (GRCm39) |
nonsense |
probably null |
|
R4710:Lamb1
|
UTSW |
12 |
31,332,582 (GRCm39) |
missense |
probably benign |
0.02 |
R4767:Lamb1
|
UTSW |
12 |
31,358,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R4809:Lamb1
|
UTSW |
12 |
31,328,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R4828:Lamb1
|
UTSW |
12 |
31,348,929 (GRCm39) |
missense |
probably benign |
|
R4842:Lamb1
|
UTSW |
12 |
31,337,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Lamb1
|
UTSW |
12 |
31,371,005 (GRCm39) |
missense |
probably benign |
0.01 |
R4909:Lamb1
|
UTSW |
12 |
31,338,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R4989:Lamb1
|
UTSW |
12 |
31,376,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R5444:Lamb1
|
UTSW |
12 |
31,348,908 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5736:Lamb1
|
UTSW |
12 |
31,352,664 (GRCm39) |
nonsense |
probably null |
|
R5766:Lamb1
|
UTSW |
12 |
31,349,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R5825:Lamb1
|
UTSW |
12 |
31,368,613 (GRCm39) |
missense |
probably benign |
|
R5840:Lamb1
|
UTSW |
12 |
31,316,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R5867:Lamb1
|
UTSW |
12 |
31,348,954 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5887:Lamb1
|
UTSW |
12 |
31,316,863 (GRCm39) |
nonsense |
probably null |
|
R5984:Lamb1
|
UTSW |
12 |
31,377,773 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6313:Lamb1
|
UTSW |
12 |
31,319,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R6359:Lamb1
|
UTSW |
12 |
31,332,715 (GRCm39) |
missense |
probably damaging |
0.97 |
R6505:Lamb1
|
UTSW |
12 |
31,373,461 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7127:Lamb1
|
UTSW |
12 |
31,374,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R7202:Lamb1
|
UTSW |
12 |
31,374,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R7271:Lamb1
|
UTSW |
12 |
31,337,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R7290:Lamb1
|
UTSW |
12 |
31,315,595 (GRCm39) |
missense |
probably benign |
0.04 |
R7486:Lamb1
|
UTSW |
12 |
31,337,441 (GRCm39) |
missense |
probably benign |
0.00 |
R7496:Lamb1
|
UTSW |
12 |
31,350,020 (GRCm39) |
missense |
probably benign |
0.31 |
R7591:Lamb1
|
UTSW |
12 |
31,376,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7722:Lamb1
|
UTSW |
12 |
31,373,570 (GRCm39) |
missense |
probably damaging |
0.99 |
R7985:Lamb1
|
UTSW |
12 |
31,350,214 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8058:Lamb1
|
UTSW |
12 |
31,353,046 (GRCm39) |
missense |
probably benign |
0.16 |
R8353:Lamb1
|
UTSW |
12 |
31,356,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R8506:Lamb1
|
UTSW |
12 |
31,379,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R8846:Lamb1
|
UTSW |
12 |
31,379,388 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8888:Lamb1
|
UTSW |
12 |
31,352,953 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8895:Lamb1
|
UTSW |
12 |
31,352,953 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9312:Lamb1
|
UTSW |
12 |
31,368,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R9340:Lamb1
|
UTSW |
12 |
31,374,224 (GRCm39) |
missense |
probably benign |
|
R9340:Lamb1
|
UTSW |
12 |
31,374,223 (GRCm39) |
missense |
probably benign |
|
R9371:Lamb1
|
UTSW |
12 |
31,348,863 (GRCm39) |
missense |
probably damaging |
0.98 |
R9417:Lamb1
|
UTSW |
12 |
31,337,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R9562:Lamb1
|
UTSW |
12 |
31,322,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R9626:Lamb1
|
UTSW |
12 |
31,354,669 (GRCm39) |
missense |
probably benign |
|
R9641:Lamb1
|
UTSW |
12 |
31,337,457 (GRCm39) |
missense |
probably damaging |
0.97 |
X0054:Lamb1
|
UTSW |
12 |
31,337,433 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Lamb1
|
UTSW |
12 |
31,353,041 (GRCm39) |
missense |
probably benign |
0.35 |
Z1176:Lamb1
|
UTSW |
12 |
31,377,701 (GRCm39) |
missense |
possibly damaging |
0.55 |
|