Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg7 |
T |
C |
16: 56,553,220 (GRCm39) |
I626V |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,588,344 (GRCm39) |
V4414E |
possibly damaging |
Het |
Ago1 |
C |
T |
4: 126,355,545 (GRCm39) |
R88H |
probably benign |
Het |
Ankrd6 |
C |
T |
4: 32,810,299 (GRCm39) |
D461N |
probably damaging |
Het |
Bcl2l14 |
A |
G |
6: 134,404,417 (GRCm39) |
N202D |
probably benign |
Het |
Bnip2 |
A |
G |
9: 69,910,686 (GRCm39) |
I245V |
probably damaging |
Het |
Cdhr3 |
T |
C |
12: 33,110,264 (GRCm39) |
D340G |
probably damaging |
Het |
Dchs1 |
T |
C |
7: 105,411,066 (GRCm39) |
E1653G |
probably damaging |
Het |
Dhdds |
C |
A |
4: 133,698,565 (GRCm39) |
Q256H |
possibly damaging |
Het |
Dsc2 |
A |
T |
18: 20,168,451 (GRCm39) |
C669* |
probably null |
Het |
Dync2h1 |
T |
C |
9: 7,135,015 (GRCm39) |
|
probably null |
Het |
Dysf |
T |
C |
6: 84,044,460 (GRCm39) |
S276P |
probably benign |
Het |
Galc |
A |
T |
12: 98,225,497 (GRCm39) |
L31* |
probably null |
Het |
Gm527 |
C |
T |
12: 64,969,184 (GRCm39) |
R204C |
possibly damaging |
Het |
Hivep3 |
G |
A |
4: 119,989,599 (GRCm39) |
D2017N |
probably benign |
Het |
Inf2 |
C |
T |
12: 112,566,752 (GRCm39) |
R106C |
probably damaging |
Het |
Itgb1 |
A |
G |
8: 129,446,786 (GRCm39) |
K434E |
probably benign |
Het |
Macc1 |
T |
G |
12: 119,410,734 (GRCm39) |
F501V |
possibly damaging |
Het |
Man2a2 |
G |
A |
7: 80,002,745 (GRCm39) |
H1079Y |
probably damaging |
Het |
Nedd4l |
G |
A |
18: 65,213,089 (GRCm39) |
V82I |
possibly damaging |
Het |
Nr2f1 |
T |
C |
13: 78,343,361 (GRCm39) |
E301G |
probably damaging |
Het |
Or10ag59 |
A |
G |
2: 87,405,715 (GRCm39) |
R96G |
probably damaging |
Het |
Or2ag13 |
A |
G |
7: 106,313,435 (GRCm39) |
L151P |
probably benign |
Het |
Or4a73 |
T |
C |
2: 89,421,040 (GRCm39) |
I140V |
probably benign |
Het |
Pdgfrb |
G |
A |
18: 61,212,004 (GRCm39) |
V844I |
possibly damaging |
Het |
Pkd1l2 |
T |
C |
8: 117,787,333 (GRCm39) |
E570G |
possibly damaging |
Het |
R3hdm4 |
A |
T |
10: 79,752,708 (GRCm39) |
L4Q |
probably damaging |
Het |
Rb1cc1 |
A |
G |
1: 6,318,415 (GRCm39) |
K639R |
probably null |
Het |
Robo3 |
A |
T |
9: 37,339,121 (GRCm39) |
C257S |
probably damaging |
Het |
Rprd2 |
A |
T |
3: 95,673,087 (GRCm39) |
L772Q |
probably damaging |
Het |
Sall2 |
T |
C |
14: 52,553,018 (GRCm39) |
D59G |
possibly damaging |
Het |
Sall3 |
T |
C |
18: 81,016,579 (GRCm39) |
T450A |
probably benign |
Het |
Sdhd |
T |
C |
9: 50,508,385 (GRCm39) |
*160W |
probably null |
Het |
Sgca |
T |
C |
11: 94,862,070 (GRCm39) |
E194G |
possibly damaging |
Het |
Shtn1 |
G |
A |
19: 59,016,616 (GRCm39) |
R228C |
probably damaging |
Het |
Skor1 |
A |
T |
9: 63,054,132 (GRCm39) |
S22T |
probably benign |
Het |
Slc26a8 |
C |
A |
17: 28,863,824 (GRCm39) |
G645V |
probably benign |
Het |
Smtn |
T |
C |
11: 3,479,988 (GRCm39) |
E411G |
probably damaging |
Het |
Sox17 |
A |
G |
1: 4,562,550 (GRCm39) |
Y217H |
probably damaging |
Het |
Syk |
A |
G |
13: 52,766,452 (GRCm39) |
Q179R |
probably benign |
Het |
Tpp2 |
A |
G |
1: 44,022,677 (GRCm39) |
I959M |
probably benign |
Het |
Trim65 |
T |
A |
11: 116,017,142 (GRCm39) |
N440I |
probably damaging |
Het |
Ubr2 |
C |
T |
17: 47,301,917 (GRCm39) |
|
probably null |
Het |
Ush2a |
T |
C |
1: 188,083,284 (GRCm39) |
S276P |
possibly damaging |
Het |
Vmn1r61 |
A |
G |
7: 5,613,430 (GRCm39) |
S295P |
probably benign |
Het |
Wdhd1 |
T |
C |
14: 47,511,481 (GRCm39) |
Q77R |
probably benign |
Het |
Xylb |
T |
A |
9: 119,220,882 (GRCm39) |
*552R |
probably null |
Het |
Zfp932 |
C |
T |
5: 110,156,694 (GRCm39) |
P131S |
probably 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 |
IGL01554:Lamb1
|
APN |
12 |
31,356,976 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|