Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adarb2 |
A |
T |
13: 8,620,455 (GRCm39) |
M314L |
probably damaging |
Het |
Apcs |
A |
G |
1: 172,722,259 (GRCm39) |
F29S |
probably damaging |
Het |
Arfgef1 |
CAGAG |
CAG |
1: 10,212,811 (GRCm39) |
|
probably null |
Het |
Avl9 |
T |
C |
6: 56,705,650 (GRCm39) |
|
probably null |
Het |
Ccdc38 |
A |
G |
10: 93,386,081 (GRCm39) |
M66V |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,258,467 (GRCm39) |
K269E |
probably benign |
Het |
Chrdl2 |
A |
C |
7: 99,678,412 (GRCm39) |
E328A |
possibly damaging |
Het |
D430041D05Rik |
T |
C |
2: 104,087,713 (GRCm39) |
N421S |
probably benign |
Het |
Dbndd1 |
G |
T |
8: 124,233,473 (GRCm39) |
Q207K |
probably benign |
Het |
Disc1 |
A |
G |
8: 125,814,874 (GRCm39) |
E246G |
probably damaging |
Het |
Dyrk4 |
A |
G |
6: 126,862,268 (GRCm39) |
I408T |
probably damaging |
Het |
Entpd7 |
G |
A |
19: 43,679,597 (GRCm39) |
R50Q |
probably benign |
Het |
Fan1 |
C |
A |
7: 64,021,292 (GRCm39) |
E591* |
probably null |
Het |
Fpr1 |
C |
A |
17: 18,097,191 (GRCm39) |
C266F |
probably benign |
Het |
Gata4 |
C |
T |
14: 63,478,146 (GRCm39) |
R151H |
possibly damaging |
Het |
Gipr |
T |
C |
7: 18,891,354 (GRCm39) |
N441S |
probably benign |
Het |
Ino80d |
G |
T |
1: 63,113,662 (GRCm39) |
Q263K |
probably benign |
Het |
Ipo13 |
A |
G |
4: 117,758,239 (GRCm39) |
I708T |
probably benign |
Het |
Iqsec3 |
A |
T |
6: 121,364,783 (GRCm39) |
Y835* |
probably null |
Het |
Kctd8 |
C |
T |
5: 69,498,617 (GRCm39) |
G10S |
probably benign |
Het |
Lcp1 |
A |
G |
14: 75,443,569 (GRCm39) |
N195S |
possibly damaging |
Het |
Or4k48 |
A |
T |
2: 111,475,871 (GRCm39) |
I157K |
possibly damaging |
Het |
Or5b121 |
T |
C |
19: 13,507,384 (GRCm39) |
S160P |
probably damaging |
Het |
Paxbp1 |
T |
C |
16: 90,840,905 (GRCm39) |
D113G |
probably damaging |
Het |
Pcdhb7 |
T |
C |
18: 37,476,141 (GRCm39) |
S426P |
probably benign |
Het |
Pcnx4 |
A |
G |
12: 72,603,076 (GRCm39) |
D446G |
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,797,011 (GRCm39) |
|
probably benign |
Het |
Pld2 |
A |
G |
11: 70,444,180 (GRCm39) |
D492G |
probably benign |
Het |
Ranbp17 |
G |
A |
11: 33,429,189 (GRCm39) |
A352V |
probably benign |
Het |
Rasgrf1 |
A |
C |
9: 89,863,797 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
C |
G |
2: 112,506,218 (GRCm39) |
R3443P |
probably damaging |
Het |
Serpinb10 |
T |
A |
1: 107,468,636 (GRCm39) |
L170H |
probably damaging |
Het |
Sfxn4 |
A |
G |
19: 60,840,501 (GRCm39) |
Y165H |
probably damaging |
Het |
Slc32a1 |
C |
T |
2: 158,453,152 (GRCm39) |
|
probably benign |
Het |
Slco5a1 |
A |
T |
1: 13,059,833 (GRCm39) |
V296D |
probably damaging |
Het |
Syn2 |
T |
A |
6: 115,204,290 (GRCm39) |
|
probably null |
Het |
Tbx2 |
C |
T |
11: 85,729,101 (GRCm39) |
Q495* |
probably null |
Het |
Trav6-1 |
G |
A |
14: 52,875,993 (GRCm39) |
V8M |
probably benign |
Het |
Usp7 |
A |
T |
16: 8,534,428 (GRCm39) |
N46K |
probably damaging |
Het |
Vmn2r58 |
A |
T |
7: 41,513,348 (GRCm39) |
F432I |
probably benign |
Het |
Vmn2r99 |
T |
C |
17: 19,599,252 (GRCm39) |
M312T |
probably benign |
Het |
Washc2 |
T |
C |
6: 116,185,165 (GRCm39) |
|
probably benign |
Het |
Yju2b |
A |
G |
8: 84,985,453 (GRCm39) |
V272A |
probably benign |
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 |
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 |
|